Publications of the Biosynthesis / NMR Research Group

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1Dudek, B., Warskulat, A.-C., Vogel, H., Wielsch, N., Menezes, R. C., Hupfer, Y., Paetz, C., Gebauer-Jung, S., Svatoš, A., Schneider, B. (2021). An integrated—omics/chemistry approach unravels enzymatic and spontaneous steps to form flavoalkaloidal nudicaulin pigments in flowers of Papaver nudicaule L. International Journal of Molecular Sciences, 22(8): 4129. doi:10.3390/ijms22084129. [NMR276] OPEN ACCESS gold MPG.PuRE
2Easson, M. L. A. E., Malka, O., Paetz, C., Hojná, A., Reichelt, M., Stein, B., van Brunschot, S., Feldmesser, E., Campbell, L., Colvin, J., Winter, S., Morin, S., Gershenzon, J., Giddings Vassão, D. (2021). Activation and detoxification of cassava cyanogenic glucosides by the whitefly Bemisia tabaci. Scientific Reports, 11: 13244. doi:10.1038/s41598-021-92553-w. [GER704] OPEN ACCESS gold MPG.PuRE
3Erdenetsogt, U., Nadmid, S., Paetz, C., Dahse, H.-M., Voigt, K., Gotov, C., Boland, W., Dagvadorj, E. (2021). New guaianolide sesquiterpene lactones and other constituents from Pyrethrum pulchrum. Planta Medica. doi:10.1055/a-1554-2866. [BOL732] MPG.PuRE
4Heiling, S., Cortés Llorca, L., Li, J., Gase, K., Schmidt, A., Schaefer, M., Schneider, B., Halitschke, R., Gaquerel, E., Baldwin, I. T. (2021). Specific decorations of 17-hydroxygeranyllinalool diterpene glycosides solve the autotoxicity problem of chemical defense in Nicotiana attenuata. The Plant Cell, 33(5), 1748-1770. doi:10.1093/plcell/koab048. [ITB627] OPEN ACCESS gelb MPG.PuRE
5Huber, M., Roder, T., Irmisch, S., Riedel, A., Gablenz, S., Fricke, J., Rahfeld, P., Reichelt, M., Paetz, C., Liechti, N., Hu, L., Meng, Y., Huang, W., Robert, C. A., Gershenzon, J., Erb, M. (2021). A beta-glucosidase of an insect herbivore determines both toxicity and deterrence of a dandelion defense metabolite. bioRxiv. doi:10.1101/2021.03.22.436380. [GER625] OPEN ACCESS gold MPG.PuRE
6Jamebozorgi, F. H., Yousefzadi, M., Firuzi, O., Nazemi, M., Zare, S., Chandran, J. N., Schneider, B., Baldwin, I. T., Jassbi, A. R. (2021). Cytotoxic furanosesquiterpenoids and steroids from Ircinia mutans sponges. Pharmaceutical Biology, 59(1), 575-583. doi:10.1080/13880209.2021.1920620. [NMR277] OPEN ACCESS gold MPG.PuRE
7Jassbi, A. R., Mirzaei, H. H., Firuzi, O., Pirhadi, S., Asadollahi, M., Chandran, J. N., Schneider, B. (2021). Cytotoxic abietane-type diterpenoids from roots of Salvia spinosa and their in Silico pharmacophore modeling. Natural Product Research. doi:10.1080/14786419.2021.1952202. [NMR278] MPG.PuRE
8Li, J., Halitschke, R., Li, D., Paetz, C., Su, H., Heiling, S., Xu, S., Baldwin, I. T. (2021). Controlled hydroxylations of diterpenoids allow for plant chemical defense without autotoxicity. Science, 371(6526), 255-260. doi:10.1126/science.abe4713. [ITB633] MPG.PuRE
9Li, L., Huang, J., Lyu, H., Guan, F., Li, P., Tian, M., Xu, S., Zhao, X., Liu, F., Paetz, C., Fenga, X., Chen, Y. (2021). Two lathyrane diterpenoid stereoisomers containing an unusual trans-gem-dimethylcyclopropane from the seeds of Euphorbia lathyris. RSC Advances, 11(5), 3183-3189. doi:10.1039/d0ra10724g. [NMR275] OPEN ACCESS gelb MPG.PuRE
10Rahman-Soad, A., Dávila-Lara, A., Paetz, C., Mithöfer, A. (2021). Plumbagin, a potent naphthoquinone from Nepenthes plants with growth inhibiting and larvicidal activities. Molecules, 26(4): 825. doi:10.3390/molecules26040825. [MIT026] OPEN ACCESS gold MPG.PuRE
11Rodríguez-López, C. E., Hong, B., Paetz, C., Nakamura, Y., Koudounas, K., Passeri, V., Baldoni, L., Alagna, F., Calderini, O., O’Connor, S. E. (2021). Two bi-functional cytochrome P450 CYP72 enzymes from olive (Olea europaea) catalyze the oxidative C-C bond cleavage in the biosynthesis of secoxy-iridoids – flavor and quality determinants in olive oil. New Phytologist, 229(4), 2288-2301. doi:10.1111/nph.16975. [SOC106] OPEN ACCESS gelb MPG.PuRE
12Schmiech, M., Ulrich, J., Lang, S. J., Büchele, B., Paetz, C., St-Gelais, A., Syrovets, T., Simmet, T. (2021). 11-keto-alpha-boswellic acid, a novel triterpenoid from Boswellia spp. with chemotaxonomic potential and antitumor activity against triple-negative breast cancer cells. Molecules, 26(2): 366. doi:10.3390/molecules26020366. [NMR272] OPEN ACCESS gold MPG.PuRE
13Soh, D., Icon, N. E., Satchet, E. M. T., Defokou, U. D., Schneider, B., Vidari, G., Nyassé, B. (2021). Antiproliferative activity of semisynthetic xylopic acid derivatives. Natural Product Research. doi:10.1080/14786419.2021.1876045. [NMR273] MPG.PuRE
14Stavenga, D. G., Leertouwer, H. L., Dudek, B., van der Kooi, C. J. (2021). Coloration of flowers by flavonoids and consequences of pH dependent absorption. Frontiers in Plant Science, 11: 600124. doi:10.3389/fpls.2020.600124. [IMPRS107] OPEN ACCESS gold MPG.PuRE
15Trenti, F., Yamamoto, K., Hong, B., Paetz, C., Nakamura, Y., O’Connor, S. E. (2021). Early and late steps of quinine biosynthesis. Organic Letters, 23(5), 1793-1797. doi:10.1021/acs.orglett.1c00206. [SOC110] OPEN ACCESS gelb MPG.PuRE
16Wirth, S., Krause, K., Kunert, M., Broska, S., Paetz, C., Boland, W., Kothe, E. (2021). Function of sesquiterpenes from Schizophyllum commune in interspecific interactions. Proceedings of the National Academy of Sciences of the United States of America, 16(1): e0245623. doi:10.1371/journal.pone.0245623. [BOL727] OPEN ACCESS gelb MPG.PuRE
17Zare, S., Hatam, G., Firuzi, O., Bagheri, A., Chandran, J. N., Schneider, B., Paetz, C., Pirhadi, S., Jassbi, A. R. (2021). Antileishmanial and pharmacophore modeling of abietane-type diterpenoids extracted from the roots of Salvia hydrangea. Journal of Molecular Structure, 1228: 129447. doi:10.1016/j.molstruc.2020.129447. [NMR274] MPG.PuRE
1Dong, C., Dolke, F., Bandi, S., Paetz, C., von Reuss, S. H. (2020). Dimerization of conserved ascaroside building blocks generates species-specific male attractants in Caenorhabditis nematodes. Organic & Biomolecular Chemistry, 18(27), 5253-5263. doi:10.1039/D0OB00799D. [BOL710] OPEN ACCESS gold MPG.PuRE
2Dudek, B., Schneider, B., Hilger, H. H., Stavenga, D. G., Martínez-Harms, J. (2020). Highly different flavonol content explains geographic variations in the UV reflecting properties of flowers of the corn poppy, Papaver rhoeas (Papaveraceae). Phytochemistry, 178: 112457. doi:10.1016/j.phytochem.2020.112457. [NMR270] MPG.PuRE
3Israni, B., Wouters, F. C., Luck, K., Seibel, E., Ahn, S.-J., Paetz, C., Reinert, M., Vogel, H., Erb, M., Heckel, D. G., Gershenzon, J., Giddings Vassão, D. (2020). The fall armyworm Spodoptera frugiperda utilizes specific UDP-glycosyltransferases to inactivate maize defensive benzoxazinoids. Frontiers in Physiology, 11: 604754. doi:10.3389/fphys.2020.604754. [GER619] OPEN ACCESS gold MPG.PuRE
4Lackus, N., Müller, A., Kröber, T., Reichelt, M., Schmidt, A., Nakamura, Y., Paetz, C., Luck, K., Lindroth, R. L., Constabel, C. P., Unsicker, S., Gershenzon, J., Köllner, T. G. (2020). The occurrence of sulfated salicinoids in poplar and their formation by sulfotransferase 1. Plant Physiology, 183(1), 137-151. doi:10.1104/pp.19.01447. [GER593] OPEN ACCESS gold MPG.PuRE
5Lang, S. J., Schmiech, M., Hafner, S., Paetz, C., Werner, K., Gaafary, M. E., Schmidt, C. Q., Syrovets, T., Simmet, T. (2020). Chrysosplenol d, a flavonol from Artemisia annua, induces ERK1/2-mediated apoptosis in triple negative human breast cancer cells. International Journal of Molecular Sciences, 21(11): 4090. doi:10.3390/ijms21114090. [NMR268] OPEN ACCESS gold MPG.PuRE
6Malka, O., Easson, M. L. A. E., Paetz, C., Götz, M., Reichelt, M., Stein, B., Luck, K., Stanišic, A., Juravel, K., Santos-Garcia, D., Mondaca, L. L., Springate, S., Colvin, J., Winter, S., Gershenzon, J., Morin, S., Giddings Vassão, D. (2020). Glucosylation prevents plant defense activation in phloem-feeding insects. Nature Chemical Biology, 16, 1429-1426. doi:10.1038/s41589-020-00658-6. [GER612] MPG.PuRE
7Nemesio-Gorriz, M., Menezes, R. C., Paetz, C., Hammerbacher, A., Steenackers, M., Schamp, K., Höfte, M., Svatoš, A., Gershenzon, J., Douglas, G. C. (2020). Canditate metabolites for ash dieback tolerance in Fraxinus excelsior. The Journal of Experimental Biology, 71(19), 6074-6083. doi:10.1093/jxb/eraa306. [MS207] MPG.PuRE
8Rodriguez, H. A., Hidalgo, W. F., Sanchez, J. D., Menezes, R. C., Schneider, B., Arango, R. E., Morales, J. G. (2020). Differential regulation of jasmonic acid pathways in resistant (Calcutta 4) and susceptible (Williams) banana genotypes during the interaction with Pseudocercospora fijiensis. Plant Pathology, 69(5), 872-882. doi:10.1111/ppa.13165. [NMR267] MPG.PuRE
9Scognamiglio, M., Schneider, B. (2020). Identification of potential allelochemicals from donor plants and their synergistic effects on the metabolome of Aegilops geniculata. Frontiers in Plant Science, 11: 1046. doi:10.3389/fpls.2020.01046. [NMR269] OPEN ACCESS gold MPG.PuRE
10Zare, S., Mirkhani, H., Firuzi, O., Moheimanian, N., Asadollahi, M., Pirhadi, S., Chandran, J. N., Schneider, B., Jassbi, A. R. (2020). Antidiabetic and cytotoxic polyhydroxylated oleanane and ursane type triterpenoids from Salvia grossheimii. Bioorganic Chemistry, 104: 104297. doi:10.1016/j.bioorg.2020.104297. [NMR271] MPG.PuRE
1Chen, Y., Paetz, C., Schneider, B. (2019). Organ-specific distribution and non-enzymatic conversions indicate a metabolic network of phenylphenalenones in Xiphidium caeruleum. Phytochemistry, 159, 30-38. doi:10.1016/j.phytochem.2018.12.004. [NMR258] MPG.PuRE
2Désiré, S., Ernestine, N., Bruno, T. B., Lazare, S. S., Ulrich, D. D., Lateef, M., Schneider, B., Ali, M. S., Barthélemy, N. (2019). A new dammarane type triterpene glucoside from the aerial parts of Gouania longipetala (Rhamnaceae). Natural Product Research. doi:10.1080/14786419.2019.1690483. [NMR265] MPG.PuRE
3Dolke, F., Dong, C., Bandi, S., Paetz, C., Glauser, G., von Reuß, S. H. (2019). Ascaroside signaling in the bacterivorous nematode Caenorhabditis remanei encodes the growth phase of its bacterial food source. Organic Letters, 21(15), 5832-5837. doi:10.1021/acs.orglett.9b01914. [BOL716] MPG.PuRE
4Fu, N., Yang, Z.-l., Pauchet, Y., Paetz, C., Brandt, W., Boland, W., Burse, A. (2019). A cytochrome P450 from juvenile mustard leaf beetles hydroxylates geraniol, a key step in iridoid biosynthesis. Insect Biochemistry and Molecular Biology, 113: 103212. doi:10.1016/j.ibmb.2019.103212. preprint available [BOL713] MPG.PuRE
5Günther, A., Schöning, I., Martin, M. J., Paetz, C. (2019). Verbreitung, Ökologie und Inhaltsstoffe von Boletopsis grisea (Peck) Bondartsev & Singer: Ein rezentes Vorkommen in Jena. Zeitschrift für Mykologie, 85(1), 31-51. [NMR259] MPG.PuRE
6Hölscher, D. (2019). Cellular-specific detection of polyphenolic compounds by NMR-and MS-based techniques. In H. Halbwirth, K. Stich, V. Cheynier, S. Quideau (Eds.), Recent Advances in Polyphenol Research (pp. 149-181). John Wiley & Sons Ltd. [NMR263] MPG.PuRE
7Lackner, S., Lackus, N., Paetz, C., Köllner, T. G., Unsicker, S. (2019). Aboveground phytochemical responses to belowground herbivory in poplar trees and the consequence for leaf herbivore preference. Plant, Cell and Environment, 42(12), 3293-3307. doi:10.1111/pce.13628. [GER578] OPEN ACCESS gelb MPG.PuRE
8Lang, S. J., Schmiech, M., Hafner, S., Paetz, C., Steinborn, C., Huber, R., Gaafary, M. E., Werner, K., Schmidt, C. Q., Syrovets, T., Simmet, T. (2019). Antitumor activity of an Artemisia annua herbal preparation and identification of active ingredients. Phytomedicine, 62: 152962. doi:10.1016/j.phymed.2019.152962. [NMR266] OPEN ACCESS gold MPG.PuRE
9Lyu, H., Liu, W., Bai, B., Shan, Y., Paetz, C., Feng, X., Chen, Y. (2019). Prenyleudesmanes and a hexanorlanostane from the roots of Lonicera macranthoides. Molecules, 24(23): 4276. doi:10.3390/molecules24234276. [NMR264] OPEN ACCESS gold MPG.PuRE
10Mirzaei, H. H., Firuzi, O., Chandran, J. N., Schneider, B., Jassbi, A. R. (2019). Two antiproliferative seco-4,5-abietane diterpenoids from roots of Salvia ceratophylla L. Phytochemistry Letters, 29, 129-133. doi:10.1016/j.phytol.2018.11.017. [NMR257] MPG.PuRE
11Schubert, T., von Reuß, S. H., Kunze, C., Paetz, C., Kruse, S., Brand-Schön, P., Nelly, A. M., Nüske, J., Diekert, G. (2019). Guided cobamide biosynthesis for heterologous production of reductive dehalogenases. Microbial Biotechnology, 12(2), 346-359. doi:10.1111/1751-7915.13339. [NMR260] OPEN ACCESS gold MPG.PuRE
12Sree, K. S., Dahse, H.-M., Chandran, J. N., Schneider, B., Jahreis, G., Appenroth, K. J. (2019). Duckweed for human nutrition: No cytotoxic and no anti-proliferative effects on human cell lines. Plant Foods for Human Nutrition, 74(2), 223-224. doi:10.1007/s11130-019-00725-x. [NMR261] MPG.PuRE
1Beran, F., Sporer, T., Paetz, C., Ahn, S.-J., Betzin, F., Kunert, G., Shekhov, A., G. Vassão, D., Bartram, S., Lorenz, S., Reichelt, M. (2018). One pathway is not enough: The cabbage stem flea beetle Psylliodes chrysocephala uses multiple strategies to overcome the glucosinolate-myrosinase defense in its host plants. Frontiers in Plant Science, 9: 1754. doi:10.3389/fpls.2018.01754. [BER004] OPEN ACCESS gold MPG.PuRE
2Berg, A., Oner, E. T., Combie, J., Schneider, B., Ellinger, R., Weisser, J., Wyrwa, R., Schnabelrauch, M. (2018). Formation of new, cytocompatible hydrogels based on photochemically crosslinkable levan methacrylates. International Journal of Biological Macromolecules, 107(Part B), 2312-2319. doi:10.1016/j.ijbiomac.2017.10.120. [NMR246] MPG.PuRE
3Carqueijeiro, I., de Bernonville, T. D., Lanoue, A., Dang, T.-T., Teijaro, C., Paetz, C., Billet, K., Mosquera, A., Oudin, A., Besseau, S., Papon, N., Glévarec, G., Atehortùa, L., Clastre, M., Giglioli-Guivarc'h, N., Schneider, B., St-Pierre, B., Andrade, R. B., O’Connor, S. E., Courdavault, V. (2018). A BAHD acyltransferase catalyzing 19-O-acetylation of tabersonine derivatives in roots of Catharanthus roseus enables combinatorial synthesis of monoterpene indole alkaloids. The Plant Journal, 49(3), 469-484. doi:10.1111/tpj.13868. [NMR249] OPEN ACCESS gold MPG.PuRE
4Chen, Y., Paetz, C., Schneider, B. (2018). Precursor-directed biosynthesis of phenylbenzoisoquinolindione alkaloids and the discovery of a phenylphenalenone-based plant defense mechanism. Journal of Natural Products, 81(4), 879-884. doi:10.1021/acs.jnatprod.7b00885. [NMR251] MPG.PuRE
5Dudek, B., Schnurrer, F., Dahse, H.-M., Paetz, C., Warskulat, A.-C., Weigel, C., Voigt, K., Schneider, B. (2018). Formation of nudicaulins in vivo and in vitro and the biomimetic synthesis and bioactivity of O-methylated nudicaulin derivatives. Molecules, 23(12): 3357. doi:10.3390/molecules23123357. [NMR256] OPEN ACCESS gold MPG.PuRE
6Feistel, F., Paetz, C., Menezes, R. C., Veit, D., Schneider, B. (2018). Acylated quinic acids are the main salicortin metabolites in the lepidopteran specialist herbivore Cerura vinula. Journal of Chemical Ecology, 44(5), 497-509. doi:10.1007/s10886-018-0945-1. [NMR253] OPEN ACCESS gelb MPG.PuRE
7Keller, A., Kunze, D., Bommer, L., Paetz, C., Menezes, R. C., Svatoš, A., Dobbek, H., Schubert, T. (2018). Selective utilization of benzimidazolyl-norcobamides as cofactors by the tetrachloroethene reductive dehalogenase of Sulfurospirillum multivorans. Journal of Bacteriology, 200(8): e00584-17. doi:10.1128/JB.00584-17. [NMR254] OPEN ACCESS gold MPG.PuRE
8Krieger, C., Roselli, S., Galati, G., Kellner-Thielmann, S., Schneider, B., Grosjean, J., Orly, A., Ritchie, D., Matern, U., Bourgaud, F., Hehn, A. (2018). The CYP71AZ P450 subfamily: a driving factor for the diversification of coumarin biosynthesis in apiaceous plants. Frontiers in Plant Science, 9: 820. doi:10.3389/fpls.2018.00820. [NMR255] OPEN ACCESS gold MPG.PuRE
9Martínez-Harms, J., Warskulat, A.-C., Dudek, B., Kunert, G., Lorenz, S., Hansson, B. S., Schneider, B. (2018). Biosynthetic and functional color-scent associations in flowers of Papaver nudicaule and its impact on pollinators. Chembiochem, 19(14), 1553-1562. doi:10.1002/cbic.201800155. [HAN307] MPG.PuRE
10Michal Johnson, J., Thürich, J., Petutschnig, E. K., Altschmied, L., Meichsner, D., Sherameti, I., Dindas, J., Mrozinska, A., Paetz, C., Scholz, S. S., Furch, A. C. U., Lipka, V., Hedrich, R., Schneider, B., Svatoš, A., Oelmüller, R. (2018). A poly(A) ribonuclease controls the cellotriose-based interaction between Piriformospora indica and its host Arabidopsis. Plant Physiology, 176(1), 2496-2514. doi:10.1104/pp.17.01423. [NMR248] OPEN ACCESS gold MPG.PuRE
11Nakamura, Y., Paetz, C., Boland, W. (2018). Synthesis of methyl 4-dihydrotrisporate B and methyl trisporate B, morphogenetic factors of Zygomycetes fungi. Zeitschrift für Naturforschung, C: Journal of Biosciences, 73(1), 59-66. doi:10.1515/znc-2017-0148. [BOL686] MPG.PuRE
12Naseri, M., Emami, S. A., Asili, J., Tayarani-Najaran, Z., Dehghan, G., Schneider, B., Iranshahi, M. (2018). Rupestrines A-D, alkaloids from the aerial parts of Corydalis rupestris. Bioorganic Chemistry, 77, 651-659. doi:10.1016/j.bioorg.2018.02.019. [NMR250] MPG.PuRE
13Soltani, S., Amin, G.-R., Salehi-Sourmaghi, M. H., Schneider, B., Lorenz, S., Iranshahi, M. (2018). Sulfur-containing compounds from the roots of Ferula latisecta and their cytotoxic activities. Fitoterapia, 124, 108-112. doi:10.1016/j.fitote.2017.10.012. [NMR247] MPG.PuRE
14Stavrinides, A. K., Tatsis, E. C., Dang, T.-T., Caputi, L., Stevenson, C. E. M., Lawson, D. M., Schneider, B., O'Connor, S. E. (2018). Discovery of a short-chain dehydrogenase from Catharanthus roseus that produces a novel monoterpene indole alkaloid. Chembiochem, 19(9), 940-948. doi:10.1002/cbic.201700621. [NMR252] MPG.PuRE
15Wang, M., Schäfer, M., Li, D., Halitschke, R., Dong, C.-F., McGale, E., Paetz, C., Song, Y., Li, S., Dong, J., Heiling, S., Groten, K., Franken, P., Bitterlich, M., Harrison, M., Paszkowski, U., Baldwin, I. T. (2018). Blumenols as shoot markers for root symbiosis with arbuscular mycorrhizal fungi. eLife, 7: e37093. doi:10.7554/eLife.37093. [ITB589] OPEN ACCESS gold MPG.PuRE
16Wirth, S., Kunert, M., Ahrens, L., Krause, K., Broska, S., Paetz, C., Kniemeyer, O., Jung, E., Boland, W., Kothe, E. (2018). The regulator of G-protein signaling Thn1 links pheromone response to volatile production in Schizophyllum commune. Environmental Microbiology, 20(10), 3684-3699. doi:10.1111/1462-2920.14369. [BOL703] MPG.PuRE
1Berasategui, A., Salem, H., Paetz, C., Santoro, M., Gershenzon, J., Kaltenpoth, M., Schmidt, A. (2017). Gut microbiota of the pine weevil degrades conifer diterpenes and increases insect fitness. Molecular Ecology, 26(15), 4099-4110. doi:10.1111/mec.14186. [GER478] MPG.PuRE
2Brkljaca, R., Schneider, B., Hidalgo, W., Otálvaro, F., Ospina, F., Lee, S., Hoshino, M., Fujita, M., Urban, S. (2017). Application of the crystalline sponge method to revise the structure of the phenalenone fuliginone. Molecules, 22(2): 211. doi:10.3390/molecules22020211. [NMR239] OPEN ACCESS gold MPG.PuRE
3Chen, Y., Paetz, C., Menezes, R. C., Schneider, B. (2017). Cultured roots of Xiphidium caeruleum: Phenylphenalenones and their biosynthetic and extractant-dependent conversion. Phytochemistry, 133, 15-25. doi:10.1016/j.phytochem.2016.10.011. [NMR237] MPG.PuRE
4Crecelius, A. C., Hölscher, D., Hoffmann, T., Schneider, B., Fischer, T. C., Hanke, M.-V., Flachowsky, H., Schwab, W., Schubert, U. S. (2017). Spatial and temporal localization of flavonoid metabolites in strawberry fruit (Fragaria × ananassa). Journal of Agricultural and Food Chemistry, 65(17), 3559-3568. doi:10.1021/acs.jafc.7b00584. [NMR241] MPG.PuRE
5Feistel, F., Paetz, C., Lorenz, S., Beran, F., Kunert, G., Schneider, B. (2017). Idesia polycarpa (Salicaceae) leaf constituents and their toxic effect on Cerura vinula and Lymantria dispar (Lepidoptera) larvae. Phytochemistry, 143, 170-179. doi:10.1016/j.phytochem.2017.08.008. [NMR245] MPG.PuRE
6Hölscher, D., Vollrath, A., Kai, M., Dhakshinamoorthy, S., Menezes, R. C., Svatoš, A., Schubert, U. S., Buerkert, A., Schneider, B. (2017). Local phytochemical response of Musa acuminata x balbisiana Colla cv. ‘Bluggoe’ (ABB) to colonization by Sternorrhyncha. Phytochemistry, 133, 26-32. doi:10.1016/j.phytochem.2016.10.007. [NMR238] MPG.PuRE
7Jassbi, A. R., Eghtesadi, F., Hazeri, N., Ma’sumi, H., Valizadeh, J., Chandran, J. N., Schneider, B., Baldwin, I. T. (2017). The roots of Salvia rhytidea: a rich source of biologically active diterpenoids. Natural Product Research, 31(4), 477-481. doi:10.1080/14786419.2016.1188096. [ITB525] MPG.PuRE
8Jassbi, A. R., Vafapour, M., Shokrollahi, A., Firuzi, O., Zare, M., Chandran, J. N., Schneider, B., Baldwin, I. T. (2017). Cytotoxic activity of two cembranoid diterpenes from Nicotiana sylvestris against three human cancer cell lines. The Open Bioactive Compounds Journal, 05, 1-8. doi:10.2174/1874847301705010001. [ITB567] OPEN ACCESS gelb MPG.PuRE
9Mageroy, M. H., Jancsik, S., Yuen, M. M. S., Fischer, M., Withers, S. G., Paetz, C., Schneider, B., MacKay, J. J., Bohlmann, J. (2017). A conifer UDP-sugar dependent glycosyltransferase contributes to acetophenone metabolism and defense against insects. Plant Physiology, 175(2), 641-651. doi:10.1104/pp.17.00611. [NMR242] OPEN ACCESS gelb MPG.PuRE
10Mirzaei, H. H., Firuzi, O., Schneider, B., Baldwin, I. T., Jassbi, A. R. (2017). Cytotoxic diterpenoids from the roots of Salvia lachnocalyx. Revista Brasileira de Farmacognosia, 27(4), 475-479. doi:10.1016/j.bjp.2017.01.009. [ITB544] OPEN ACCESS gelb MPG.PuRE
11Ocampos, F. M. M., Paetz, C., Antar, G. M., Menezes, R. C., Miguel, O. G., Schneider, B. (2017). Phytochemical profile of Schiekia orinocensis (Haemodoraceae). Phytochemistry Letters, 21, 139-145. doi:10.1016/j.phytol.2017.06.008. [NMR244] MPG.PuRE
12Ospina, F., Ramirez, A., Cano, M., Hidalgo, W., Schneider, B., Otálvaro, F. (2017). Synthesis of positional isomeric phenylphenalenones. The Journal of Organic Chemistry, 82(7), 3873-3879. doi:10.1021/acs.joc.6b02985. [NMR240] MPG.PuRE
13Schneider, B. (2017). Phenylphenalenone glycosides: Occurrence, structure revision, and substituent effects on the steric orientation. Phytochemistry Letters, 21, 104-108. doi:10.1016/j.phytol.2017.06.004. [NMR243] MPG.PuRE
14Wang, M., Schoettner, M., Xu, S., Paetz, C., Wilde, J., Baldwin, I. T., Groten, K. (2017). Catechol, a major component of smoke, influences primary root growth and root hair elongation through reactive oxygen species-mediated redox signaling. New Phytologist, 213(4), 1755-1770. doi:10.1111/nph.14317. [ITB534] OPEN ACCESS gold MPG.PuRE
1Boeckler, A., Paetz, C., Feibicke, P., Gershenzon, J., Unsicker, S. (2016). Metabolism of poplar salicinoids by the generalist herbivore Lymantria dispar (Lepidoptera). Insect Biochemistry and Molecular Biology, 78, 39-49. doi:10.1016/j.ibmb.2016.08.001. [GER456] MPG.PuRE
2Chen, Y., Paetz, C., Menezes, R. C., Schneider, B. (2016). Phenylbenzoisoquinolindione alkaloids accumulate in stamens of Xiphidium caeruleum Aubl. flowers. Phytochemistry, 128, 95-101. doi:10.1016/j.phytochem.2016.05.002. [NMR230] MPG.PuRE
3Dudek, B., Warskulat, A.-C., Schneider, B. (2016). The occurrence of flavonoids and related compounds in flower sections of Papaver nudicaule. Plants, 5: 28. doi:10.3390/plants5020028. [NMR229] OPEN ACCESS gold MPG.PuRE
4Fang, J., Ramsay, A., Renouard, S., Hano, C., Lamblin, F., Chabbert, B., Mesnard, F., Schneider, B. (2016). Laser microdissection and spatiotemporal pinoresinol-lariciresinol reductase gene expression assign the cell layer-specific accumulation of secoisolaricirésinol diglucoside in flaxseed coats. Frontiers in Plant Science, 7: 1743. doi:10.3389/fpls.2016.01743. [NMR236] OPEN ACCESS gold MPG.PuRE
5Handrick, V., Robert, C. A. M., Ahern, K. R., Zhou, S., Machado, R. A. R., Maag, D., Glauser, G., Fernandez-Penny, F. E., Chandran, J. N., Rodgers-Melnike, E., Schneider, B., Buckler, E. S., Boland, W., Gershenzon, J., Jander, G., Erb, M., Köllner, T. G. (2016). Biosynthesis of 8-O-methylated benzoxazinoid defense compounds in maize. The Plant Cell, 28(7), 1682-1700. doi:10.1105/tpc.16.00065. [GER442] OPEN ACCESS gold MPG.PuRE
6Hidalgo, W., Cano, M., Arbelaez, M., Zarrazola, E., Gil, J., Schneider, B., Otálvaro, F. (2016). 4-Phenylphenalenones as a template for new photodynamic compounds against Mycosphaerella fijiensis. Pest Management Science, 72(4), 796-800. doi:10.1002/ps.4055. [NMR222] MPG.PuRE
7Hidalgo, W., Chandran, J. N., Menezes, R. C., Otálvaro, F., Schneider, B. (2016). Phenylphenalenones protect banana plants from infection by Mycosphaerella fijiensis and are deactivated by metabolic conversion. Plant, Cell and Environment, 39(3), 492-513. doi:10.1111/pce.12630. [NMR223] OPEN ACCESS gelb MPG.PuRE
8Hölscher, D., Buerkert, A., Schneider, B. (2016). Phenylphenalenones accumulate in plant tissues of two banana cultivars in response to herbivory by the banana weevil and banana stem weevil. Plants, 5(3): 34. doi:10.3390/plants5030034. [NMR233] OPEN ACCESS gold MPG.PuRE
9Iranshahy, M., Tayarani-Najaran, Z., Kasaian, J., Ghandadi, M., Emami, S. A., Asili, J., Chandran, J. N., Schneider, B., Iranshahi, M. (2016). Highly oxygenated sesquiterpene lactones from Cousinia aitchisonii and their cytotoxic properties: Rhaserolide induces apoptosis in human T lymphocyte (Jurkat) cells via the activation of c-Jun N-terminal kinase phosphorylation. Phytotherapy Research, 30(2), 222-226. doi:10.1002/ptr.5519. [NMR226] MPG.PuRE
10Jassbi, A. R., Firuzi, O., Miri, R., Salhei, S., Zare, S., Zare, M., Masroorbabanari, M., Chandran, J. N., Schneider, B., Baldwin, I. T. (2016). Cytotoxic activity and chemical constituents of Anthemis mirheydari. Pharmaceutical Biology, 54(10), 2044-2049. doi:10.3109/13880209.2016.1141220. [ITB515] MPG.PuRE
11Jassbi, A. R., Mirzaei, Y., Firuzi, O., Chandran, J. N., Schneider, B. (2016). Bioassay guided purification of cytotoxic natural products from a red alga Dichotomaria obtusata. Revista Brasileira de Farmacognosia, 26(6), 705-709. doi:10.1016/j.bjp.2016.06.008. [NMR232] OPEN ACCESS gelb MPG.PuRE
12Liu, Y., Luo, S.-H., Schmidt, A., Wang, G.-D., Sun, G.-L., Grant, M., Kuang, C., Yang, M.-J., Jing, S.-X., Li, C.-H., Schneider, B., Gershenzon, J., Li, S.-H. (2016). A geranylfarnesyl diphosphate synthase provides the precursor for sesterterpenoid (C25) formation in the glandular trichomes of the mint Leucosceptrum canum. The Plant Cell, 28(3), 804-822. doi:10.1105/tpc.15.00715. [GER436] OPEN ACCESS gold MPG.PuRE
13Ospina, F., Hidalgo, W., Cano, M., Schneider, B., Otálvaro, F. (2016). Synthesis of 8-Phenylphenalenones: 2-Hydroxy-8-(4-hydroxyphenyl)-1H-phenalen-1-one from Eichhornia crassipes. The Journal of Organic Chemistry, 81(3), 1256-1262. doi:10.1021/acs.joc.5b02559. [NMR228] MPG.PuRE
14Paetz, C., Hammerbacher, A., Menezes, R. C., Feistel, F., Weigel, C., Voigt, K., Schneider, B. (2016). Chemical composition and antimicrobial activity of Populus nigra shoot resin. Natural Product Communications, 11(7), 989-992. doi:10.1177/1934578X1601100730. [NMR231] MPG.PuRE
15Pauls, G., Becker, T., Rahfeld, P., Gretscher, R., Paetz, C., Pasteels, J., von Reuss, S. H., Burse, A., Boland, W. (2016). Two defensive lines in juvenile leaf beetles; esters of 3-nitropropionic acid in the hemo­lymph and aposematic warning. Journal of Chemical Ecology, 42(3), 240-248. doi:10.1007/s10886-016-0684-0. [BOL645] MPG.PuRE
16Ramsay, A., Fliniaux, O., Quéro, A., Molinie, R., Dly, H., Hano, C., Paetz, C., Roscher, A., Grand, E., Kovensky, J., Schneider, B., Mesnard, F. (2016). Kinetics of the incorporation of the main phenolic compounds into the lignan macromolecule during flaxseed development. Food Chemistry, 217, 1-8. doi:10.1016/j.foodchem.2016.08.039. [NMR234] MPG.PuRE
17Ritter, M., Seidel, R. A., Bellstedt, P., Schneider, B., Bauer, M., Görls, H., Pohnert, G. (2016). Isolation and identification of intermediates of the oxidative bilirubin degradation. Organic Letters, 18(17), 4432-4435. doi:10.1021/acs.orglett.6b02287. [FGP001] MPG.PuRE
18Stanton, M., Preßler, J., Paetz, C., Boland, W., Svatoš, A., Baldwin, I. T. (2016). Plant-mediated pheromone emission by a hemipteran seed feeder increases the apparency of an unreliable but rewarding host. New Phytologist, 211(1), 113-125. doi:10.1111/nph.13879. [ITB516] OPEN ACCESS gold MPG.PuRE
19Wadke, N., Kandasamy, D., Vogel, H., Lah, L., Wingfield, B. D., Paetz, C., Wright, L., Gershenzon, J., Hammerbacher, A. (2016). The bark-beetle-associated fungus, Endoconidiophora polonica, utilizes the phenolic defense compounds of its host as a carbon source. Plant Physiology, 171(2), 914-931. doi:10.1104/pp.15.01916. [GER448] OPEN ACCESS gold MPG.PuRE
20Warskulat, A.-C., Tatsis, E., Dudek, B., Kai, M., Lorenz, S., Schneider, B. (2016). An unprecedented utilization of pelargonidin and indole for the biosynthesis of plant indole alkaloids. Chembiochem, 17(4), 318-327. doi:10.1002/cbic.201500572. [NMR227] OPEN ACCESS gold MPG.PuRE
1Baranovskii, A. V., Bolibrukh, D. A., Schneider, B. (2015). Synthesis of 14alpha-substituted Androstanes—key compounds in the synthesis of 14-substituted Brassinosteroids. Russian Journal of Organic Chemistry, 51(1), 78-85. doi:10.1134/S1070428015010133. [NMR216] MPG.PuRE
2Baranovsky, A., Bolibrukh, D. A., Schneider, B. (2015). Solvolysis of 14,17-etheno-bridged 16alpha-nitroestratrienyl acetate and lactam formation pathways studied by LC-NMR and LC-MS. Structures of minor products. Steroids, 104, 37-48. doi:10.1016/j.steroids.2015.08.009. [NMR224] MPG.PuRE
3Becker, T., Kartikeya, P., Paetz, C., von Reuß, S. H., Boland, W. (2015). Synthesis and photosensitivity of isoxazolin-5-one glycosides. Organic & Biomolecular Chemistry, 13, 4025-4030. doi:10.1039/C5OB00244C. [BOL618] OPEN ACCESS gold MPG.PuRE
4Boachon, B., Junker, R. R., Miesch, L., Bassard, J.-E., Höfer, R., Caillieaudeaux, R., Seidel, D. E., Lesot, A., Heinrich, C., Ginglinger, J.-F., Allouche, L., Vincent, B., Wahyuni, D. S., Paetz, C., Beran, F., Miesch, M., Schneider, B., Leiss, K., Werck-Reichhart, D. (2015). CYP76C1 (Cytochrome P450)-mediated linalool metabolism and the formation of volatile and soluble Linalool oxides in Arabidopsis flowers: A strategy for defense against floral antagonists. The Plant Cell, 27(10), 2972-2990. doi:10.1105/tpc.15.00399. [NMR225] OPEN ACCESS gold MPG.PuRE
5Chitsazian-Yazdi, M., Agnolet, S., Lorenz, S., Schneider, B., Es’haghi, Z., Kasaian, J., Khameneh, B., Iranshahi, M. (2015). Foetithiophenes C-F, thiophene derivatives from the roots of Ferula foetida. Pharmaceutical Biology, 53(5), 710-714. doi:10.3109/13880209.2014.939765. [NMR211] MPG.PuRE
6Fatangare, A., Paetz, C., Saluz, H., Svatoš, A. (2015). 2-Deoxy-2-fluoro-D-glucose metabolism in Arabidopsis thaliana. Frontiers in Plant Science, 6: 935. doi:10.3389/fpls.2015.00935. [MS174] OPEN ACCESS gold MPG.PuRE
7Feistel, F., Paetz, C., Lorenz, S., Schneider, B. (2015). The absolute configuration of salicortin, HCH-salicortin and tremulacin from Populus trichocarpa × deltoides Beaupré. Molecules, 20, 5566-5573. doi:10.3390/molecules20045566. [NMR217] OPEN ACCESS gold MPG.PuRE
8Gaafary, M. E., Büchele, B., Syrovets, T., Agnolet, S., Schneider, B., Schmidt, C. Q., Simmet, T. (2015). An alpha-acetoxy-tirucallic acid isomer inhibits Akt/mTOR signaling and induces oxidative stress in prostate cancer cells. Journal of Pharmacology and Experimental Therapeutics, 352(1), 33-42. doi:10.1124/jpet.114.217323. [NMR213] MPG.PuRE
9González-Cabanelas, D., Wright, L., Paetz, C., Onkokesung, N., Gershenzon, J., Concepción, M. R., Phillips, M. A. (2015). The diversion of 2-C-methyl-D-erythritol-2,4-cyclodiphosphate from the 2-C-methyl-D-erythritol 4-phosphate pathway to hemiterpene glycosides mediates stress responses in Arabidopsis thaliana. The Plant Journal, 82(1), 122-137. doi:10.1111/tpj.12798. [GER405] OPEN ACCESS gold MPG.PuRE
10Hidalgo, W., Kai, M., Schneider, B. (2015). 4-Methoxycinnamic acid – An unusual phenylpropanoid involved in phenylphenalenone biosynthesis in Anigozanthos preissii. Phytochemistry, 117, 476-481. doi:10.1016/j.phytochem.2015.05.017. [NMR221] OPEN ACCESS gold MPG.PuRE
11Hölscher, D., Fuchser, J., Knop, K., Menezes, R. C., Buerkert, A., Svatoš, A., Schubert, U. S., Schneider, B. (2015). High resolution mass spectrometry imaging reveals the occurrence of phenylphenalenone-type compounds in red paracytic stomata and red epidermis tissue of Musa acuminata ssp. zebrina cv. ‘Rowe Red’. Phytochemistry, 116, 239-245. doi:10.1016/j.phytochem.2015.04.010. [NMR218] MPG.PuRE
12Huber, M., Triebwasser-Freese, D., Reichelt, M., Heiling, S., Paetz, C., Chandran, J. N., Bartram, S., Schneider, B., Gershenzon, J., Erb, M. (2015). Identification, quantification, spatiotemporal distribution and genetic variation of major latex secondary metabolites in the common dandelion (Taraxacum officinale agg.). Phytochemistry, 115, 89-98. doi:10.1016/j.phytochem.2015.01.003. [GER406] MPG.PuRE
13Kamarozaman, A. S., Latip, J., Paetz, C., Syah, Y. M. (2015). Monomer stilbenoid glucosides from Vatica pauciflora and Vatica lowii (Dipterocarpaceae). Jurnal Teknologi, 77(2), 69-72. doi:10.11113/jt.v77.5989. [NMR262] OPEN ACCESS gold MPG.PuRE
14Lu, X., Dittgen, J., Pislewska-Bednarek, M., Molina, A., Schneider, B., Svatoš, A., Doubský, J., Schneeberger, K., Weigel, D., Bednarek, P., Schulze-Lefert, P. (2015). Mutant allele-specific uncoupling of PENETRATION3 functions reveals engagement of the ATP-binding cassette transporter in distinct tryptophan metabolic pathways. Plant Physiology, 168, 814-827. doi:10.1104/pp.15.00182. [MS170] OPEN ACCESS gelb MPG.PuRE
15Martin, N. J., Ferreiro, S. F., Barbault, F., Nicolas, M., Lecellier, G., Paetz, C., Gaysinski, M., Alonso, E., Thomas, O. P., Botana, L. M., Raharivelomanana, P. (2015). Indole alkaloids from the Marquesan plant Rauvolfia nukuhivensis and their effects on ion channels. Phytochemistry, 109, 84-95. doi:10.1016/j.phytochem.2014.10.026. [NMR235] MPG.PuRE
16Morgenstern, A., Paetz, C., Behrend, A., Spiteller, D. (2015). Divalent transition-metal-ion stress induces Prodigiosin biosynthesis in Streptomyces coelicolor M145: formation of Coeligiosins. Chemistry – A European Journal, 21(16), 6027-6032. doi:10.1002/chem.201405733. [BOL619] MPG.PuRE
17Poreddy, S., Mitra, S., Schöttner, M., Chandran, J. N., Schneider, B., Baldwin, I. T., Kumar, P., Pandit, S. S. (2015). Detoxification of hostplant’s chemical defense rather than its anti-predator co-option drives beta-glucosidase-mediated lepidopteran counter-adaptation. Nature Communications, 6: 8525. doi:10.1038/ncomms9525. [ITB506] OPEN ACCESS gold MPG.PuRE
18Schläger, S., Beran, F., Groot, A. T., Ulrichs, C., Veit, D., Paetz, C., Karumuru, B. R. M., Srinivasan, R., Schreiner, M., Mewis, I. (2015). Pheromone blend analysis and cross-attraction among populations of Maruca vitrata from Asia and West Africa. Journal of Chemical Ecology, 41, 1155-1162. doi:10.1007/s10886-015-0653-z. [BER003] MPG.PuRE
19Shokoohinia, Y., Sajjadi, S.-E., Jassbi, A. R., Moradi, H., Ghassemi, N., Schneider, B. (2015). Sesquiterpenes and flavonoids of Anthemis odontostephana var. odontostephana. Chemistry of Natural Compounds, 51(3), 491-494. doi:10.1007/s10600-015-1322-8. [NMR220] MPG.PuRE
20Zenger, K., Agnolet, S., Schneider, B., Kraus, B. (2015). Biotransformation of flavokawains A, B and C, chalcones from Kava (Piper methysticum), by human liver microsomes. Journal of Agricultural and Food Chemistry, 63(28), 6376-6385. doi:10.1021/acs.jafc.5b01858. [NMR219] MPG.PuRE
1Falk, K., Kästner, J., Bodenhausen, N., Schramm, K., Paetz, C., G. Vassão, D., Reichelt, M., von Knorre, D., Bergelson, J., Erb, M., Gershenzon, J., Meldau, S. (2014). The role of glucosinolates and the jasmonic acid pathway in resistance of Arabidopsis thaliana against molluskan herbivores. Molecular Ecology, 23(5), 1188-1203. doi:10.1111/mec.12610. [GER357] MPG.PuRE
2Fang, J., Schneider, B. (2014). Laser microdissection: a sample preparation technique for plant micrometabolic profiling. Phytochemical Analysis, 25, 307-313. doi:10.1002/pca.2477. [NMR202] MPG.PuRE
3Hammerbacher, A., Paetz, C., Wright, L., Fischer, T. C., Bohlmann, J., Davis, A. J., Fenning, T. M., Gershenzon, J., Schmidt, A. (2014). Flavan-3-ols in Norway spruce: Biosynthesis, accumulation and function in response to attack by the bark beetle-associated fungus Ceratocystis polonica. Plant Physiology, 164, 2107-2122. doi:10.1104/pp.113.232389. [GER379] OPEN ACCESS gelb MPG.PuRE
4Hölscher, D., Dhakshinamoorthy, S., Alexandrov, T., Becker, M., Bretschneider, T., Bürkert, A., Crecelius, A. C., De Waele, D., Elsen, A., Heckel, D. G., Heklau, H., Hertweck, C., Kai, M., Knop, K., Krafft, C., Maddula, R. K., Matthäus, C., Popp, J., Schneider, B., Schubert, U., Sikora, R., Svatoš, A., Swennen, R. (2014). Phenalenone-type phytoalexins mediate resistance of banana plants (Musa spp.) to the burrowing nematode Radopholus similis. Proceedings of the National Academy of Sciences of the United States of America, 111(1), 105-110. doi:10.1073/pnas.1314168110. [NMR205] OPEN ACCESS gold MPG.PuRE
5Keller-Costa, T., Hubbard, P. C., Paetz, C., Nakamura, Y., da Silva, J. P., Rato, A., Barata, E. N., Schneider, B., Canario, A. V. M. (2014). Identity of a tilapia pheromone released by dominant males that primes females for reproduction. Current Biology, 24(18), 2130-2135. doi:10.1016/j.cub.2014.07.049. [NMR212] OPEN ACCESS gold MPG.PuRE
6Kia, S. H., Schulz, M., Ayah, E., Schouten, A., Müllenborn, C., Paetz, C., Schneider, B., Hofmann, D., Disko, U., Tabaglio, V., Marocco, A. (2014). Abutilon theophrasti’s defense against the allelochemical benzoxazolin-2(3H)-one: support by Actinomucor elegans. Journal of Chemical Ecology, 40(11-12), 1286-1298. doi:10.1007/s10886-014-0529-7. [NMR215] MPG.PuRE
7Monakhova, Y., Schneider, B. (2014). The intramolecular Diels-Alder reaction of diarylheptanoids – quantum chemical calculation of structural features favoring the formation of phenylphenalenones. Molecules, 19, 5231-5242. doi:10.3390/molecules19045231. [NMR208] OPEN ACCESS gold MPG.PuRE
8Nagel, R., Berasategui, A., Paetz, C., Gershenzon, J., Schmidt, A. (2014). Overexpression of an isoprenyl diphosphate synthase in spruce leads to unexpected terpene diversion products that function in plant defense. Plant Physiology, 164(2), 555-569. doi:10.1104/pp.113.228940. [GER356] OPEN ACCESS gelb MPG.PuRE
9Nakamura, Y., Paetz, C., Brandt, W., David, A., Rendón-Anaya, M., Herrera-Estrella, A., Mithöfer, A., Boland, W. (2014). Synthesis of 6-substituted 1-oxoindanoyl isoleucine conjugates and modeling studies with the COI1-JAZ co-receptor complex of lima bean. Journal of Chemical Ecology, 40, 687-699. doi:10.1007/s10886-014-0469-2. [BOL601] MPG.PuRE
10Ramsay, A., Fliniaux, O., Fang, J., Molinie, R., Roscher, A., Grand, E., Guillot, X., Kovensky, J., Fliniaux, M.-A., Schneider, B., Mesnard, F. (2014). Development of an NMR metabolomics-based tool for selection of flaxseed varieties. Metabolomics, 10, 1258-1267. doi:10.1007/s11306-014-0664-8. [NMR207] MPG.PuRE
11Rasool, A., Joußen, N., Lorenz, S., Ellinger, R., Schneider, B., Khan, S. A., Ashfaq, M., Heckel, D. G. (2014). An independent occurrence of the chimeric P450 enzyme CYP337B3 of Helicoverpa armigera confers cypermethrin resistance in Pakistan. Insect Biochemistry and Molecular Biology, 53, 54-65. doi:10.1016/j.ibmb.2014.07.006. [HEC282] MPG.PuRE
12Schneider, B. (2014). Chemical Ecology. In M. J. Simpson, A. J. Simpson (Eds.), NMR Spectroscopy: A Versatile Tool for Environmental Research (pp. 223-242). Chichester, UK: John Wiley & Sons Ltd. [NMR210] MPG.PuRE
13Tatsis, E., Eylert, E., Maddula, R. K., Ostrozhenkova, E., Svatoš, A., Eisenreich, W., Schneider, B. (2014). Biosynthesis of nudicaulins. A 13CO2-pulse/chase labeling study with Papaver nudicaule. Chembiochem, 15, 1645-1650. doi:10.1002/cbic.201402109. [NMR209] MPG.PuRE
1Besseau, S., Kellner, F., Lanoue, A., Thamm, A. M., Salim, V., Schneider, B., Geu-Flores, F., Höfer, R., Guirimand, G., Guihur, A., Oudin, A., Glevarec, G., Foureau, E., Papon, N., Clastre, M., Giglioli-Guivarc’h, N., St-Pierre, B., Werck-Reichhart, D., Burlat, V., Luca, V. D., O'Connor, S. E., Courdavault, V. (2013). A pair of tabersonine 16-hydroxylases initiates the synthesis of vindoline in an organ dependent manner in Catharanthus roseus. Plant Physiology, 163(4), 1792-1803. doi:10.1104/pp.113.222828. [NMR203] OPEN ACCESS gold MPG.PuRE
2Buch, F., Rott, M., Rottloff, S., Paetz, C., Hilke, I., Raessler, M., Mithöfer, A. (2013). Secreted pitfall-trap fluid of carnivorous Nepenthes plants is unsuitable for microbial growth. Annals of Botany, 111(3), 375-383. doi:10.1093/aob/mcs287. [BOL551] OPEN ACCESS gold MPG.PuRE
3de Souza, G. D., Mithöfer, A., Daolio, C., Schneider, B., Rodrigues-Filho, E. (2013). Identification of Alternaria alternata mycotoxins by LC-SPE-NMR and their cytotoxic effects to soybean (Glycine max) cell suspension culture. Molecules and Cells, 18, 2528-2538. doi:10.3390/molecules18032528. [BOL556] OPEN ACCESS gelb MPG.PuRE
4Duque, L., Zapata, C., Rojano, B., Schneider, B., Otalvaro, F. (2013). Radical scavenging capacity of 2,4-dihydroxy-9-phenyl-1H-phenalen-1-one: A functional group exclusion approach. Organic Letters, 15(14), 3542-3545. doi:10.1021/ol400384z. [NMR201] MPG.PuRE
5Fang, J., Ramsay, A., Paetz, C., Tatsis, E., Renouard, S., Hano, C., Grand, E., Fliniaux, O., Roscher, A., Mesnard, F., Schneider, B. (2013). Concentration kinetics of secoisolariciresinol diglucoside and its biosynthetic precursor coniferin in developing flaxseed. Phytochemical Analysis, 24(1), 41-46. doi:10.1002/pca.2377. [NMR188] MPG.PuRE
6Ginglinger, J.-F., Boachon, B., Höfer, R., Paetz, C., Köllner, T., Lugan, R., Mutterer, J., Fischer, M., Ullmann, P., Beran, F., Claudel, P., Baltenweck, R., Miesch, L., Verstappen, F., Bouwmeester, H., Miesch, M., Schneider, B., Gershenzon, J., Ehlting, J., Werck-Reichhart, D. (2013). Gene coexpression analysis reveals a complex metabolism of the monoterpene alcohol linalool in Arabidopsis flowers. The Plant Cell, 25(11), 4640-4657. doi:10.1105/tpc.113.117382. [GER362] OPEN ACCESS gold MPG.PuRE
7Hammerbacher, A., Schmidt, A., Wadke, N., Wright, L., Schneider, B., Bohlmann, J., Brand, W., Fenning, T. M., Gershenzon, J., Paetz, C. (2013). A common fungal associate of the spruce bark beetle metabolizes the stilbene defenses of Norway spruce. Plant Physiology, 162, 1324-1336. doi:10.1104/pp.113.218610. [GER344] OPEN ACCESS gelb MPG.PuRE
8Happyana, N., Agnolet, S., Muntendam, R., van Dam, A., Schneider, B., Kayser, O. (2013). Analysis of cannabinoids in laser-microdissected trichomes of medicinal Cannabis sativa using LCMS and cryogenic NMR. Phytochemistry, 87, 51-59. doi:10.1016/j.phytochem.2012.11.001. [NMR196] MPG.PuRE
9Heinrich, M., Hettenhausen, C., Lange, T., Wünsche, H., Fang, J., Baldwin, I. T., Wu, J. (2013). High levels of jasmonic acid antagonize the biosynthesis of gibberellins and inhibit the growth of Nicotiana attenuata stems. The Plant Journal, 73(4), 591-606. doi:10.1111/tpj.12058. [ITB397] OPEN ACCESS gold MPG.PuRE
10Irmisch, S., Clavijo McCormick, A. L., Boeckler, A., Schmidt, A., Reichelt, M., Schneider, B., Block, K., Schnitzler, J.-P., Gershenzon, J., Unsicker, S., Köllner, T. (2013). Two herbivore-induced cytochrome P450 enzymes CYP79D6 and CYP79D7 catalyze the formation of volatile aldoximes involved in poplar defense. The Plant Cell, 25(11), 4737-4754. doi:10.1105/tpc.113.118265. [GER361] OPEN ACCESS gold MPG.PuRE
11Kunert, M., Rahfeld, P., Shaker, K. H., Schneider, B., David, A., Dettner, K., Pasteels, J. M., Boland, W. (2013). Beetles do it differently: Two stereodivergent cyclisation modes in iridoid-producing leaf-beetle larvae. ChemBioChem, 14, 353-360. doi:10.1002/cbic.201200689. [BOL561] MPG.PuRE
12Li, C.-H., Jing, S.-X., Luo, S.-H., Shi, W., Hua, J., Liu, Y., Li, X.-N., Schneider, B., Gershenzon, J., Li, S.-H. (2013). Peltate glandular trichomes of Colquhounia coccinea var. Mollis Harbor a new class of defensive sesterterpenoids. Organic Letters, 15(7), 1694-1697. doi:10.1021/ol4004756. [GER342] MPG.PuRE
13Miosic, S., Knop, K., Hölscher, D., Greiner, J., Gosch, C., Thill, J., Kai, M., Shrestha, B. K., Schneider, B., Crecelius, A. C., Schubert, U. S., Svatoš, A., Stich, K., Halbwirth, H. (2013). 4-Deoxyaurone formation in Bidens ferulifolia (Jacq.) DC. PLoS One, 8(5): e61766. doi:10.1371/journal.pone.0061766. [MS147] OPEN ACCESS gold MPG.PuRE
14Munde, T., Brand, S., Hidalgo, W., Maddula, R. K., Svatoš, A., Schneider, B. (2013). Biosynthesis of tetraoxygenated phenylphenalenones in Wachendorfia thyrsiflora. Phytochemistry, 91, 165-176. doi:10.1016/j.phytochem.2012.02.020. [NMR187] MPG.PuRE
15Pardo-Torre, J., Schmidt, G., Paetz, C., Reichelt, M., Schneider, B., Gershenzon, J., D'Auria, J. (2013). The biosynthesis of hydroxycinnamoyl quinate esters and their role in the storage of cocaine in Erythroxylum coca. Phytochemistry, 91, 177-186. doi:10.1016/j.phytochem.2012.09.009. [GER346] MPG.PuRE
16Schneider, B. (2013). Chemical Ecology. In R. K. Harris, R. E. Wasylishen (Eds.), eMagRes (pp. 451-466). John Wiley and Sons. doi:10.1002/9780470034590.emrstm1341. [NMR204] MPG.PuRE
17Soh, D., Nkwengoua, E., Ngantchou, I., Nyasse, B., Denier, C., Hannaert, V., Shaker, K. H., Schneider, B. (2013). Xylopioxyde and other bioactive kaurane-diterpenes from Xylopia aethiopica Dunal (Annonaceae). Journal of Applied Pharmaceutical Science, 3(12), 013-019. [NMR206] MPG.PuRE
18Tatsis, E., Böhm, H., Schneider, B. (2013). Occurrence of nudicaulin structural variants in flowers of papaveraceous species. Phytochemistry, 105-112. doi:10.1016/j.phytochem.2013.04.011. [NMR200] MPG.PuRE
19Tatsis, E., Schaumlöffel, A., Warskulat, A.-C., Massiot, G., Schneider, B., Bringmann, G. (2013). Nudicaulins, yellow flower pigments of Papaver nudicaule: Revised constitution and assignment of absolute configuration. Organic Letters, 15(1), 156-159. doi:10.1021/ol303211w. [NMR198] MPG.PuRE
1Baranovsky, A. V., Bolibrukh, D. A., Khripach, V. A., Schneider, B. (2012). Diels–Alder reaction of androsta-14,16-dien-17-yl acetates with nitroethylene: Product distribution and selected adduct transformations. Steroids, 78, 282-287. doi:10.1016/j.steroids.2012.11.015. [NMR199] MPG.PuRE
2Cano, M., Rojas, C., Hidalgo, W., Sáez, J., Gil, J., Schneider, B., Otálvaro, F. (2012). Improved synthesis of 4-phenylphenalenones: the case of isoanigorufone and structural analogs. Tetrahedron Letters, 54, 351-354. doi:10.1016/j.tetlet.2012.11.118. [NMR197] MPG.PuRE
3Cervellati, C., Paetz, C., Dondini, L., Tartarini, S., Bassi, D., Schneider, B., Masia, A. (2012). A qNMR approach for bitterness phenotyping and QTL identification in an F1 apricot progeny. Journal of Biotechnology, 159, 312-319. doi:10.1016/j.jbiotec.2011.09.004. [NMR185] MPG.PuRE
4Daolio, C., Schneider, B. (2012). Coupling liquid chromatography and other separation techniques to nuclear magnetic resonance spectroscopy. In Hyphenated and Alternative Methods of Detection in Chromatography (pp. 61-98). [NMR184] MPG.PuRE
5Docimo, T., Reichelt, M., Schneider, B., Kai, M., Kunert, G., Gershenzon, J., D'Auria, J. (2012). The first step in the biosynthesis of cocaine in Erythroxylum coca: the characterization of arginine and ornithine decarboxylases. Plant Molecular Biology, 78(6), 599-615. doi:10.1007/s11103-012-9886-1. [GER321] MPG.PuRE
6Fang, J., Hölscher, D., Schneider, B. (2012). Co-occurrence of phenylphenalenones and flavonoids in Xiphidium caeruleum Aubl. flowers. Phytochemistry, 82, 143-148. doi:10.1016/j.phytochem.2012.07.005. [NMR192] MPG.PuRE
7Fang, J., Kai, M., Schneider, B. (2012). Phytochemical profile of aerial parts and roots of Wachendorfia thyrsiflora L. studied by LC-DAD-SPE-NMR. Phytochemistry, 81, 144-152. doi:10.1016/j.phytochem.2012.05.023. [NMR190] MPG.PuRE
8Fang, J., Reichelt, M., Hidalgo, W., Agnolet, S., Schneider, B. (2012). Tissue-specific distribution of secondary metabolites in rapeseed (Brassica napus). PLoS One, 7(10): e48006. doi:10.1371/journal.pone.0048006. [NMR194] OPEN ACCESS gold MPG.PuRE
9Fang, J., Reichelt, M., Kai, M., Schneider, B. (2012). Metabolic profiling of lignans and other secondary metabolites from rapeseed (Brassica napus L.). Journal of Agricultural and Food Chemistry, 60, 10523-10529. doi:10.1021/jf303907b. [NMR193] MPG.PuRE
10Iranshahi, M., Amanolahi, F., Schneider, B. (2012). New sesquiterpene coumarin from the roots of Ferula latisecta. Avicenna Journal of Phytomedicine, 2(3), 133-138. [NMR191] OPEN ACCESS gold MPG.PuRE
11Jirschitzka, J., Schmidt, G., Reichelt, M., Schneider, B., Gershenzon, J., D'Auria, J. (2012). Plant tropane alkaloid biosynthesis evolved independently in the Solanaceae and Erythroxylaceae. Proceedings of the National Academy of Sciences of the United States of America, 109(26), 10304-10309. doi:10.1073/pnas.1200473109. [GER328] OPEN ACCESS gold MPG.PuRE
12Joußen, N., Agnolet, S., Lorenz, S., Schöne, S. E., Ellinger, R., Schneider, B., Heckel, D. G. (2012). Resistance of Australian Helicoverpa armigera to fenvalerate is due to the chimeric P450 enzyme CYP337B3. Proceedings of the National Academy of Sciences of the United States of America, 109(38), 15206-15211. doi:10.1073/pnas.1202047109. [HEC230] OPEN ACCESS gold MPG.PuRE
13Kaur, H., Shaker, K. H., Heinzel, N., Ralph, J., Galis, I., Baldwin, I. T. (2012). Environmental stresses of field growth allow cinnamyl alcohol dehydrogenase-deficient Nicotiana attenuata plants to compensate for their structural deficiencies. Plant Physiology, 159(4), 1545-1570. doi:10.1104/pp.112.196717. [ITB374] OPEN ACCESS gelb MPG.PuRE
14Krafft, C., Cervellati, C., Paetz, C., Schneider, B., Popp, J. (2012). Distribution of amygdalin in apricot (Prunus armeniaca) seeds studied by Raman microscopic imaging. Applied Spectroscopy, 66(6), 644-649. doi:10.1366/11-06521. [NMR189] MPG.PuRE
15Li, S.-H., Nagy, N. E., Hammerbacher, A., Krokene, P., Niu, X.-M., Gershenzon, J., Schneider, B. (2012). Localization of phenolics in phloem parenchyma cells of Norway spruce (Picea abies). ChemBioChem: A European Journal of Chemical Biology, 13, 2707-2713. doi:10.1002/cbic.201200547. [NMR195] MPG.PuRE
16Luo, S.-H., Liu, Y., Hua, J., Niu, X.-M., Jing, S.-X., Zhao, X., Schneider, B., Gershenzon, J., Li, S.-H. (2012). Unique proline-benzoquinone pigment from the colored nectar of “Bird’s Coca Cola Tree” functions in bird attractions. Organic Letters, 14(16), 4146-4149. doi:10.1021/ol3017879. [GER319] MPG.PuRE
17Schoenian, I., Paetz, C., Dickschat, J. S., Aigle, B., Leblond, P., Spiteller, D. (2012). An unprecedented 1,2-shift in the biosynthesis of the 3-aminosalicylate moiety of antimycins. ChemBioChem, 13(6), 769-773. doi:10.1002/cbic.201200033. [BOL523] MPG.PuRE
18Yan, Y.-M., Dai, H.-Q., Du, Y., Schneider, B., Guo, H., Li, D.-P., Zhang, L.-X., Fu, H., Dong, X.-P., Cheng, Y.-X. (2012). Identification of blapsins A and B as potent small-molecule 14-3-3 inhibitors from the insect Blaps japanensis. Bioorganic & Medicinal Chemistry Letters, 22(12), 4179-4181. doi:10.1016/j.bmcl.2012.04.027. [NMR186] MPG.PuRE
1Ahn, S.-J., Badenes-Pérez, F. R., Reichelt, M., Svatoš, A., Schneider, B., Gershenzon, J., Heckel, D. G. (2011). Metabolic detoxification of capsaicin by UDP-glycosyltransferase in three Helicoverpa species. Archives of Insect Biochemistry and Physiology, 78(2), 104-118. doi:10.1002/arch.20444. [HEC198] MPG.PuRE
2Berg, A., Wyrwa, R., Weisser, J., Weiss, T., Schade, R., Hildebrand, G., Liefeith, K., Schneider, B., Ellinger, R., Schnabelrauch, M. (2011). Synthesis of photopolymerizable hydrophilic macromers and evaluation of their applicability as reactive resin components for the fabrication of three-dimensionally structured hydrogel matrices by 2-photon-polymerization. Advanced Engineering Materials, 13(9), B274-B284. doi:10.1002/adem.201080092. [NMR144] MPG.PuRE
3Fang, J., Paetz, C., Hölscher, D., Munde, T., Schneider, B. (2011). Phenylphenalenones and related natural products from Wachendorfia thyrsiflora L. Phytochemistry Letters, 4(2), 203-208. doi:10.1016/j.phytol.2011.03.006. [NMR181] MPG.PuRE
4Fang, J., Paetz, C., Schneider, B. (2011). C-methylated flavanones and dihydrochalcones from Myrica gale seeds. Biochemical Systematics and Ecology, 39(1), 68-70. doi:10.1016/j.bse.2011.01.009. [NMR095] MPG.PuRE
5Frölich, N., Dees, C., Paetz, C., Ren, X., Lohse, M. J., Nikolaev, V. O., Zenk, M. H. (2011). Distinct pharmacological properties of morphine metabolites at Gi-protein and b-arrestin signaling pathways activated by the human m-opioid receptor. Biochemical Pharmacology, 81(10), 1248-1254. doi:10.1016/j.bcp.2011.03.001. [NMR165] MPG.PuRE
6Morad, S. A., Schmidt, C., Büchele, B., Schneider, B., Wenzler, M., Syrovets, T., Simmet, T. (2011). (8R)-3ß,8-Dihydroxypolypoda-13E,17E,21-triene induces cell cycle arrest and apoptosis in treatment-resistant prostate cancer cells. Journal of Natural Products, 74, 1731-1736. doi:10.1021/np200161a. [NMR183] MPG.PuRE
7Munde, T., Maddula, R. K., Svatoš, A., Schneider, B. (2011). The biosynthetic origin of oxygen functions in phenylphenalenones of Anigozanthos preissii inferred from NMR- and HRMS-based isotopologue analysis. Phytochemistry, 72, 49-58. doi:10.1016/j.phytochem.2010.10.007. [NMR118] MPG.PuRE
8Nganso, Y. O. D., Ngantchou, I. E. W., Nkwenoua, E., Nyasse, B., Denier, C., Hannert, V., Schneider, B. (2011). Preparation antitrypanosomal and cytotoxic activities of 22-hydroxyclerosterol, a new sterol from Allexis cauliflora (Violaceae). Scientia Pharmaceutica, 79(1), 137-144. doi:10.3797/scipharm.1012-10. [NMR154] OPEN ACCESS gold MPG.PuRE
9Rempt, M., Schneider, B., Pohnert, G. (2011). A reactive conjugated allene involved in the biosynthesis of volatile oxylipins in the moss Dicranum scoparium. Organic Letters, 13, 3229-3231. doi:10.1021/ol201114g. [NMR182] MPG.PuRE
10Schneider, B. (2011). Nuclear magnetic resonance spectroscopic analysis of enzyme products. Progress in Botany, 72, 183-208. doi:10.1007/978-3-642-13145-5_7. [NMR115] MPG.PuRE
11Shao, Y., Spiteller, D., Tang, X., Ping, L., Colesie, C., Münchberg, U., Bartram, S., Schneider, B., Büdel, B., Popp, J., Heckel, D. G., Boland, W. (2011). Crystallization of a- and ß-carotene in the foregut of Spodoptera larvae feeding on a toxic food plant. Insect Biochemistry and Molecular Biology, 41(4), 273-281. doi:10.1016/j.ibmb.2011.01.004. [BOL506] MPG.PuRE
12Weinhold, A., Shaker, K. H., Wenzler, M., Schneider, B., Baldwin, I. T. (2011). Phaseoloidin, a homogentisic acid glucoside from Nicotiana attenuata trichomes, contributes to the plant’s resistance against Lepidopteran herbivores. Journal of Chemical Ecology, 37, 1091-1098. doi:10.1007/s10886-011-0012-7. [ITB333] MPG.PuRE
13Ziaei, A., Ramezani, M., Wright, L., Paetz, C., Schneider, B., Amirghofran, Z. (2011). Identification of spathulenol in Salvia mirzayanii and the immunomodulatory effects. Phytotherapy Research, 25(4), 557-562. doi:10.1002/ptr.3289. [NMR153] MPG.PuRE
1Bartsch, M., Bednarek, P., Vivancos, P. D., Schneider, B., von Röpenack-Lahaye, E., Foyer, C., Kombrink, E., Scheel, D., Parker, J. E. (2010). Accumulation of isochorismate-derived 2,3-dihydroxybenzoic 3-O-ß-D-xyloside in Arabidopsis resistance to pathogens and ageing of leaves. The Journal of Biological Chemistry, 285, 25654-25665. doi:10.1074/jbc.M109.092569. [NMR114] OPEN ACCESS gold MPG.PuRE
2Bürkert, A., Khanjari, S. A., Al-Saady, N. A., De Langhe, E., Hölscher, D., Gebauer, J., Behrendt, S., Happe, S., Brinkmann, K., Schlecht, E. (2010). Wie sich Oasen-Bananen gegen ihre Feinde wehren. Uralter Toleranzmechanismus im Oman entdeckt. Biologie in unserer Zeit, 40(5), 334-341. doi:10.1002/biuz.201010432. [NMR119] MPG.PuRE
3Dagvadorj, E., Shaker, K. H., Windsor, D., Schneider, B., Boland, W. (2010). Phenolic glucosides from Hasseltia floribunda. Phytochemistry, 71(16), 1900-1907. doi:10.1016/j.phytochem.2010.08.004. [BOL409] MPG.PuRE
4Drach, S., Khripach, V., Litvinovskaya, R., Lyakhov, A., Schneider, B., Zhylitskaya, H. (2010). Stereoselective synthesis of 9a-hydroxylated ecdysteroids. Steroids, 75(2), 184-188. doi:10.1016/j.steroids.2009.10.011. [NMR094] MPG.PuRE
5Duque, L., Restrepo, C., Sáez, J., Gil, J., Schneider, B., Otálvaro, F. (2010). Synthesis of musafluorone: A naphthoxanthenone isolated from Musa acuminata. Tetrahedron Letters, 51(35), 4640-4643. doi:10.1016/j.tetlet.2010.06.128. [NMR116] MPG.PuRE
6Gosch, C., Halbwirth, H., Schneider, B., Hölscher, D., Stich, K. (2010). Cloning and heterologous expression of glycosyltransferases from Malus x domestica and Pyrus communis, which convert phloretin to phloretin 2'-O-glucoside (phloridzin). Plant Science, 178(3), 299-306. doi:10.1016/j.plantsci.2009.12.009. [NMR180] MPG.PuRE
7Heiling, S., Schuman, M. C., Schöttner, M., Mukerjee, P., Berger, B., Schneider, B., Jassbi, A., Baldwin, I. T. (2010). Jasmonate and ppHsystemin regulate key malonylation steps in the biosynthesis of 17-hydroxygeranyllinalool diterpene glycosides, an abundant and effective direct defense against herbivores in Nicotiana attenuata. The Plant Cell, 22(1), 273-292. doi:10.1105/tpc.109.071449. [ITB140] OPEN ACCESS gold MPG.PuRE
8Iranshahi, M., Kalategi, F., Sahebkar, A., Sardashti, A., Schneider, B. (2010). New sesquiterpene coumarins from the roots of Ferula flabelliloba. Pharmaceutical Biology, 48(2), 217-220. doi:10.3109/13880200903019226. [NMR093] MPG.PuRE
9Jitsaeng, K., Paetz, C., Schneider, B. (2010). Phenylphenalenones from Musa cv. 'Thepanom' (BBB). Records of Natural Products, 4(1), 26-30. [NMR065] OPEN ACCESS gold MPG.PuRE
10Jitsaeng, K., Schneider, B. (2010). Metabolic profiling of Musa acuminata challenged with Sporobolomyces salmonicolor. Phytochemistry Letters, 3(2), 84-87. doi:10.1016/j.phytol.2010.02.001. [NMR099] MPG.PuRE
11Khripach, V., Zhabinskii, V., Zhiburtovich, Y., Ivanova, G., Konstantinova, O., Tsavlovskii, D., Lorenz, S., Schneider, B. (2010). Preparation and synthetic application of partially protected brassinosteroids. Steroids, 75(1), 27-33. doi:10.1016/j.steroids.2009.09.010. [NMR179] MPG.PuRE
12Kroiß, J., Kaltenpoth, M., Schneider, B., Schwinger, M.-G., Hertweck, C., Maddula, R. K., Strohm, E., Svatos, A. (2010). Symbiotic streptomycetes provide antibiotic combination prophylaxis for wasp offspring. Nature Chemical Biology, 6, 261-263. doi:10.1038/nchembio.331. [KAL001] MPG.PuRE
13Luo, S.-H., Luo, Q., Niu, X., Xie, M.-J., Zhao, X., Schneider, B., Gershenzon, J., Li, S.-H. (2010). Glandular trichomes of Leucosceptrum canum harbor defensive sesterterpenoids. Angewandte Chemie International Edition, 49, 4471-4475. doi:10.1002/ange.201000449. [GER280] MPG.PuRE
14Ngantchou, I., Nyasse, B., Denier, C., Blonski, C., Hannaert, V., Schneider, B. (2010). Antitrypanosomal alkaloids from Polyalthia suaveolens (Annonaceae): their effects on three selected glycolytic enzymes of Trypanosoma brucei. Bioorganic & Medicinal Chemistry Letters, 20(12), 3495-3498. doi:10.1016/j.bmcl.2010.04.145. [NMR112] MPG.PuRE
15Otálvaro, F., Jitsaeng, K., Munde, T., Echeverri, F., Quinones, W., Schneider, B. (2010). O-Methylation of phenylphenalenone phytoalexins in Musa acuminata and Wachendorfia thyrsiflora. Phytochemistry, 71(2-3), 206-213. doi:10.1016/j.phytochem.2009.10.019. [NMR177] MPG.PuRE
16Shaker, K. H., Morsy, N., Zinecker, H., Imhoff, J., Schneider, B. (2010). Secondary metabolites from Calotropis procera (Aiton). Phytochemistry Letters, 3(4), 212-216. doi:10.1016/j.phytol.2010.07.009. [NMR117] MPG.PuRE
17Shaker, K., Zinecker, H., Ghani, M., Imhoff, J., Schneider, B. (2010). Bioactive metabolites from the sponge Suberea sp. Chemistry and Biodiversity, 7(12), 2880-2887. doi:10.1002/cbdv.200900277. [NMR096] MPG.PuRE
1Bednarek, P., Pislewska-Bednarek, M., Svatos, A., Schneider, B., Doubský, J., Mansourova, M., Humphry, M., Consonni, C., Panstruga, R., Sanchez-Vallet, A., Molina, A., Schulze-Lefert, P. (2009). A glucosinolate metabolism pathway in living plant cells mediates broad-spectrum antifungal defense. Science, 323, 101-106. [MS128] MPG.PuRE
2Hidalgo, W., Duque, L., Saez, J., Arango, R., Gil, J., Rojano, B., Schneider, B., Otálvaro, F. (2009). Structure-activity relationship in the interaction of substituted perinaphthenones with Mycosphaerella fijiensis. Journal of Agricultural and Food Chemistry, 57(16), 7417-7421. doi:10.1021/jf901052e. [NMR176] MPG.PuRE
3Hölscher, D., Shroff, R., Knop, K., Gottschaldt, M., Crecelius, A., Schneider, B., Heckel, D. G., Schubert, U. S., Svatos, A. (2009). Matrix-free UV-laser desorption/ionization (LDI) mass spectrometric imaging at the single-cell level: Distribution of secondary metabolites of Arabidopsis thaliana and Hypericum species. The Plant Journal, 60(5), 907-918. doi:10.1111/j.1365-313X.2009.04012.x. [MS118] OPEN ACCESS gold MPG.PuRE
4Iranshahi, M., Noroozi, A., Behravan, J., Karimi, G., Schneider, B. (2009). Persicasulphide C, a new sulphur-containing derivative from Ferula persica. Natural Product Research, 23(17), 1584-1588. doi:10.1080/14786410802393571. [NMR178] MPG.PuRE
5Jean, T. P., Shaari, K., Paetz, C., Ismail, I. S., Abas, F., Lajis, N. H., Ahmad, V. U. (2009). Bidesmosidic oleanane saponins from Xerospermum noronhianum. Helvetica Chimica Acta, 92(10), 1973-1982. doi:10.1002/hlca.200900063. [NMR019] MPG.PuRE
6Jitsaeng, K., De Eknamkul, W., Schneider, B. (2009). Flavonoids and a new calamenene-type sesquiterpene from rhizomes of Alpinia oxymitra K. Schum (Zingiberaceae). Records of Natural Products, 3(2), 110-113. [NMR171] OPEN ACCESS gold MPG.PuRE
7Knill, T., Reichelt, M., Paetz, C., Gershenzon, J., Binder, S. (2009). Arabidopsis thaliana encodes a bacterial-type heterodimeric isopropylmalate isomerase involved in both Leu biosynthesis and the Met chain elongation pathway of glucosinolate formation. Plant Molecular Biology Reporter, 71(3), 227-239. doi:10.1007/s11103-009-9519-5. [GER269] MPG.PuRE
8Larbat, R., Hehn, A., Hans, J., Schneider, S., Jugdé, H., Schneider, B., Matern, U., Bourgaud, F. (2009). Isolation and functional characterization of CYP71AJ4 encoding for the first P450 monooxygenase of angular furanocoumarin biosynthesis. The Journal of Biological Chemistry, 284(8), 4776-4785. doi:10.1074/jbc.M807351200. [NMR168] OPEN ACCESS gold MPG.PuRE
9Lusebrink, I., Dettner, K., Schierling, A., Müller, T., Daolio, C., Schneider, B., Schmidt, J., Seifert, K. (2009). New pyridine alkaloids from rove beetles of the genus Stenus (Coleoptera: Staphylinidae). Zeitschrift für Naturforschung, C: Journal of Biosciences, 64(3-4), 271-278. doi:10.1515/znc-2009-3-420. [NMR172] MPG.PuRE
10Maulidiani, Shaari, K., Paetz, C., Stanslas, J., Abas, F., Lajis, N. H. (2009). Naturally occurring labdane diterpene and benzofuran from Globba pendula. Natural Product Communications, 4(8), 1031-1036. doi:10.1177/1934578X0900400803. [NMR017] MPG.PuRE
11Moco, S., Schneider, B., Vervoort, J. (2009). Plant micrometabolomics: the analysis of endogenous metabolites present in a plant cell or tissue. Journal of Proteome Research, 8(4), 1694-1703. doi:10.1021/pr800973r. [NMR170] MPG.PuRE
12Ngantchou, I., Nkwengoua, E., Nganso, Y., Nyasse, B., Denier, C., Hannaert, V., Schneider, B. (2009). Antitrypanosomal activity of polycarpol from Piptostigma preussi (Annonaceae). Fitoterapia, 80(3), 188-191. doi:10.1016/j.fitote.2009.01.008. [NMR169] MPG.PuRE
13Nkwengoua, E., Ngantchou, I., Nyasse, B., Denier, C., Blonski, C., Schneider, B. (2009). in vitro inhibitory effects of palmatine from Enantia chlorantha on Trypanosoma cruzi and Leishmania infantum. Natural Product Research, 23(12), 1144-1150. doi:10.1080/14786410902726241. [NMR175] MPG.PuRE
14Nyasse, B., Nono, J.-J., Nganso, Y., Ngantchou, I., Schneider, B. (2009). Uapaca genus (Euphorbiaceae), a good source of betulinic acid. Fitoterapia, 80(1), 32-34. doi:10.1016/j.fitote.2008.09.005. [NMR167] MPG.PuRE
1Abdullah, Y., Schneider, B., Petersen, M. (2008). Occurrence of rosmarinic acid, chlorogenic acid and rutin in Marantaceae species. Phytochemistry Letters, 1, 199-203. doi:10.1016/j.phytol.2008.09.010. [NMR174] MPG.PuRE
2Baranovsky, A. V., Bolibrukh, D. A., Khripach, V. A., Schneider, B. (2008). A new approach to heterocycle-modified steroids via nitrile oxide intermediates. Arkivoc, 9, 29-41. [NMR163] OPEN ACCESS gold MPG.PuRE
3Berim, A., Ebel, R., Schneider, B., Petersen, M. (2008). UDP-glucose:(6-methoxy)podophyllotoxin 7-O-glucosyltransferase from suspension cultures of Linum nodiflorum. Phytochemistry, 69(2), 374-381. doi:10.1016/j.phytochem.2007.07.030. [NMR159] MPG.PuRE
4Hölscher, D., Brand, S., Wenzler, M., Schneider, B. (2008). NMR-based metabolic profiling of Anigozanthos floral nectar. Journal of Natural Products, 71(2), 251-257. doi:10.1021/np0705514. [NMR173] MPG.PuRE
5Hölscher, D., Schneider, B. (2008). Application of laser-assisted microdissection for tissue and cell-specific analysis of RNA, proteins, and metabolites. Progress in Botany, 69, 141-167. doi:10.1007/978-3-540-72954-9_6. [NMR157] MPG.PuRE
6Iranshahi, M., Mojarab, M., Sadeghian, H., Hanafi-Bojd, M. Y., Schneider, B. (2008). Polar secondary metabolites of Ferula persica roots. Phytochemistry, 69(2), 473-478. doi:10.1016/j.phytochem.2007.08.001. [NMR155] MPG.PuRE
7Khripach, V., Zhabinskii, V. N., Fando, G. P., Khripach, N. B., Schneider, B. (2008). Synthesis and radical oxidation of steroidal 1-oxo-5-alpha-alcohols. ARKIVOC, 9, 20-28. doi:10.3998/ark.5550190.0009.903. [NMR162] OPEN ACCESS gold MPG.PuRE
8Khripach, V., Zhabinskii, V., Antonchick, A., Litvinovskaya, R., Drach, S., Sviridov, O., Pryadko, A., Novik, T., Matveentsev, V., Schneider, B. (2008). A new type of modified brassinosteroids for enzyme-linked immunosorbent assay. Natural Product Communications, 3(5), 735-748. doi:10.1177/1934578X0800300513. [NMR160] MPG.PuRE
9Köllner, T. G., Schnee, C., Li, S., Svatos, A., Schneider, B., Gershenzon, J., Degenhardt, J. (2008). Protonation of a neutral (S)-beta-bisabolene intermediate is involved in (S)-beta-macrocarpene formation by the maize sesquiterpene synthases TPS6 and TPS11. The Journal of Biological Chemistry, 283(30), 20779-20788. doi:10.1074/jbc.M802682200. [GER245] OPEN ACCESS gold MPG.PuRE
10Li, S. H., Niu, X. M., Zahn, S., Gershenzon, J., Weston, J., Schneider, B. (2008). Diastereomeric stilbene glucoside dimers from the bark of Norway spruce (Picea abies). Phytochemistry, 69(3), 772-782. [NMR156] MPG.PuRE
11Murgu, M., Santos, A., Souza, D., Daolio, C., Schneider, B., Ferreira, A. G., Rodrigues-Filho, E. (2008). Hydroxylation of a hederagenin derived saponin by a xylareaceous fungus found in fruits of Sapindus saponaria. Journal of the Brazilian Chemical Society, 9, 831-835. doi:10.1590/S0103-50532008000500004. [NMR164] OPEN ACCESS gold MPG.PuRE
12Nanclares, J., Gil, J., Rojano, B., Saez, J., Schneider, B., Otalvaro, F. (2008). Synthesis of 4-methoxy-1H-phenalen-1-one: a subunit related to natural phenalenone-type compounds. Tetrahedron Letters, 49(24), 3844-3847. doi:10.1016/j.tetlet.2008.04.095. [NMR161] MPG.PuRE
13Tao, Q. F., Xu, Y., Lam, R. Y. Y., Schneider, B., Dou, H., Leung, P. S., Shi, S. Y., Zhou, C. X., Yang, L. X., Zhang, R. P., Xiao, Y. C., Wu, X., Stöckigt, J., Zeng, S., Cheng, C. H. K., Zhao, Y. (2008). Diarylheptanoids and a monoterpenoid from the rhizomes of Zingiber officinale: antioxidant and cytoprotective properties. Journal of Natural Products, 71(1), 12-17. doi:10.1021/np070114p. [NMR158] MPG.PuRE
14Vergara, F., Wenzler, M., Hansen, B. G., Kliebenstein, D. J., Halkier, B. A., Gershenzon, J., Schneider, B. (2008). Determination of the absolute configuration of the glucosinolate methyl sulfoxide group reveals a stereospecific biosynthesis of the side chain. Phytochemistry, 69(15), 2737-2742. doi:10.1016/j.phytochem.2008.09.008. [GER248] MPG.PuRE
15Wenzler, M., Hölscher, D., Oerther, T., Schneider, B. (2008). Nectar formation and floral nectary anatomy of Anigozanthos flavidus - a combined magnetic resonance imaging and spectroscopy study. Journal of Experimental Botany, 59(12), 3425-3434. doi:10.1093/jxb/ern191. [NMR166] OPEN ACCESS gold MPG.PuRE
1Berim, A., Schneider, B., Petersen, M. (2007). Methyl allyl ether formation in plants: novel S-adenosyl L-methionine:coniferyl alcohol 9-O-methyltransferase from suspension cultures of three Linum species. Plant Molecular Biology, 64(3), 279-291. doi:10.1007/s11103-007-9151-1. [NMR147] MPG.PuRE
2Emami, S. A., Amin-Ar-Ramimeh, E., Ahi, A., Kashy, M. R. B., Schneider, B., Iranshahi, M. (2007). Prenylated flavonoids and flavonostilbenes from Sophora pachycarpa roots. Pharmaceutical Biology, 45(6), 453-457. doi:10.1080/13880200701389078. [NMR150] MPG.PuRE
3Hemmati, S., Schneider, B., Schmidt, T., Federolf, K., Alfermann, A. W., Fuss, E. (2007). Justicidin B 7-hydroxylase, a cytochrome P450 monooxygenase from cell cultures of Linum perenne Himmelszelt involved in the biosynthesis of diphyllin. Phytochemistry, 68(22-24), 2736-2743. doi:10.1016/j.phytochem.2007.10.025. [NMR152] MPG.PuRE
4Khripach, V. A., Khripach, N. B., Zhabinskii, V. N., Zhiburtovich, Y. Y., Schneider, B., Degroot, A. T. (2007). Synthesis of [7,7-2H2]epibrassinolide. Journal of Labelled Compounds and Radiopharmaceuticals, 50(13), 1153-1158. doi:10.1002/jlcr.1408. [NMR151] MPG.PuRE
5Li, S. H., Schneider, B., Gershenzon, J. (2007). Microchemical analysis of laser-microdissected stone cells of Norway spruce by cryogenic nuclear magnetic resonance spectroscopy. Planta, 225(3), 771-779. doi:10.1007/s00425-006-0376-z. [NMR139] MPG.PuRE
6Otalvaro, F., Nanclares, J., Estella, L., Quinones, W., Echeverri, W., Arango, R., Schneider, B. (2007). Phenalenone-type compounds from Musa acuminata var. "Yangambi km 5" (AAA) and their activity against Mycosphaerella fijensis. Journal of Natural Products, 70(5), 887-890. doi:10.1021/np070091e. [NMR148] MPG.PuRE
7Schneider, B. (2007). Nuclear magnetic resonance spectroscopy in biosynthetic studies. Progress in Nuclear Magnetic Resonance Spectroscopy, 51(3), 155-198. doi:10.1016/j.pnmrs.2007.02.006. [NMR146] MPG.PuRE
8Schneider, B., Hölscher, D. (2007). Laser microdissection and cryogenic nuclear magnetic resonance spectroscopy: an alliance for cell type-specific metabolite profiling. Planta, 225(3), 763-770. doi:10.1007/s00425-006-0404-z. [NMR141] MPG.PuRE
9Vdovitchenko, M. Y., Kuzovkina, I. N., Paetz, C., Schneider, B. (2007). Formation of phenolic compounds in the roots of Hedysarum theinum cultured in vitro. Russian Journal of Plant Physiology, 54(4), 536-544. [NMR149] MPG.PuRE
1Antonchik, A. P., Svatos, A., Konstantinova, O. V., Zhabinskii, V. N., Khripach, V. A., Schneider, B. (2006). Reversible conversion in the brassinosteroid quartet castasterone, brassinolide and their 3 beta-epimers. Zeitschrift für Naturforschung, B: A Journal of Chemical Sciences, 61(8), 1039-1044. doi:10.1515/znb-2006-0817. [NMR138] OPEN ACCESS gold MPG.PuRE
2Brand, S., Holscher, D., Schierhorn, A., Svatos, A., Schroder, J., Schneider, B. (2006). A type III polyketide synthase from Wachendorfia thyrsiflora and its role in diarylheptanoid and phenylphenalenone biosynthesis. Planta, 224(2), 413-428. doi:10.1007/s00425-006-0228-x. [NMR137] MPG.PuRE
3Buchele, B., Zugmaier, W., Estrada, A., Genze, F., Syrovets, T., Paetz, C., Schneider, B., Simmet, T. (2006). Characterization of 3 alpha-acetyl-11-keto-alpha-boswellic acid, a pentacyclic triterpenoid inducing apoptosis in vitro and in vivo. Planta Medica, 72(14), 1285-1289. doi:10.1055/s-2006-951680. [NMR143] MPG.PuRE
4Cheng, Y., Schneider, B., Riese, U., Schubert, B., Li, Z., Hamburger, M. (2006). (+)-N-deoxymillitarinone A, a neuritogenic pyridone alkaloid from the insect pathogenic fungus Paecilomyces farinosus. Journal of Natural Products, 69(3), 436-438. doi:10.1021/np050418g. [NMR135] MPG.PuRE
5Hölscher, D., Reichert, M., Gorls, H., Ohlenschlager, O., Bringmann, G., Schneider, B. (2006). Monolaterol, the first configurationally assigned phenylphenalenone derivative with a stereogenic center at C-9, from Monochoria elata. Natural Product Reports, 69(11), 1614-1617. doi:10.1021/np060192x. [NMR142] MPG.PuRE
6Nyasse, B., Ngantchou, I., Nono, J.-J., Schneider, B. (2006). Antifilarial activity in vitro of polycarpol and 3-O-acetyl aleuritolic acid from Cameroonian medicinal plants against Onchocerca gutturosa. Natural Product Research, 20(4), 391-397. doi:10.1080/14786410600661377. [NMR136] MPG.PuRE
7Schliemann, W., Schneider, B., Wray, V., Schmidt, E., Nimtz, M., Porzel, A., Böhm, H. (2006). Flavonols and an indole alkaloid skeleton bearing identical acylated glycosidic groups from yellow petals of Papaver nudicaule. Phytochemistry, 67(2), 191-201. doi:10.1016/j.phytochem.2005.11.002. [NMR131] MPG.PuRE
8Vergara, F., Svatoš, A., Schneider, B., Reichelt, M., Gershenzon, J., Wittstock, U. (2006). Glycine conjugates in a lepidopteran insect herbivore - The metabolism of benzylglucosinolate in the cabbage white butterfly, Pieris rapae. Chembiochem, 7(12), 1982-1989. doi:10.1002/cbic.200600280. [GER369] MPG.PuRE
9Vogelsang, K., Schneider, B., Petersen, M. (2006). Production of rosmarinic acid and a new rosmarinic acid 3 '-O-beta-D-glucoside in suspension cultures of the hornwort Anthoceros agrestis Paton. Planta, 223(2), 369-373. doi:10.1007/s00425-005-0089-8. [NMR102] MPG.PuRE
1Antonchik, A. P., Svatos, A., Schneider, B., Konstantinova, O. V., Zhabinskii, V. N., Khripach, V. A. (2005). 2,3-Epoxybrassinosteroids are intermediates in the biosynthesis of castasterone in seedlings of Secale cereale. Phytochemistry, 66(1), 65-72. doi:10.1016/j.phytochem.2004.11.008. [NMR087] MPG.PuRE
2Bednarek, P., Schneider, B., Svatos, A., Oldham, N. J., Hahlbrock, K. (2005). Structural complexity, differential response to infection, and tissue specificity of indolic and phenylpropanoid secondary metabolism in Arabidopsis roots. Plant Physiology, 138(2), 1058-1070. doi:10.1104/pp.104.057794. [NMR089] OPEN ACCESS gold MPG.PuRE
3Cheng, Y., Schneider, B., Oberthür, C., Graf, H., Adler, S., Hamburger, M. (2005). Flavone C-glycosides from Isatis tinctoria leaves. Heterocycles, 65(7), 1655-1661. doi:10.3987/COM-05-10343. [NMR091] MPG.PuRE
4Hölscher, D., Schneider, B. (2005). The biosynthesis of 8-phenylphenalenones from Eichhornia crassipes involves a putative aryl migration step. Phytochemistry, 66(1), 59-64. doi:10.1016/j.phytochem.2004.10.019. [NMR086] MPG.PuRE
5Khripach, V. A., Zhabinskii, V. N., Konstantinova, O. V., Khripach, N. B., Antonchik, A. V., Antonchik, A. P., Schneider, B. (2005). Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids. Steroids, 70(8), 551-562. doi:10.1016/j.steroids.2005.02.014. [NMR088] MPG.PuRE
6Kuzovkina, I. N., Schneider, B. (2005). Genetically transformed root cultures - generation, properties and application in plant sciences. Progress in Botany, 67, 275-314. doi:10.1007/3-540-27998-9_13. [NMR092] MPG.PuRE
7Schneider, B., Paetz, C., Hölscher, D., Opitz, S. (2005). HPLC-NMR for tissue-specific analysis of phenylphenalenone-related compounds in Xiphidium caeruleum (Haemodoraceae). Magnetic Resonance in Chemistry, 43(9), 724-728. doi:10.1002/mrc.1634. [NMR090] MPG.PuRE
1Antonchik, A. P., Schneider, B., Zhabinskii, V. N., Khripach, V. A. (2004). Synthesis of [26,27-H-2H6] brassinosteroids from 23,24-bisnorcholenic acid methyl ester. Steroids, 69(10), 617-628. doi:10.1016/j.steroids.2004.05.014. [NMR084] MPG.PuRE
2Bednarek, P., Winter, J., Hamberger, B., Oldham, N. J., Schneider, B., Tan, J.-W., Hahlbrock, K. (2004). Induction of 3 '-O-beta-D-ribofuranosyl adenosine during compatible, but not during incompatible, interactions of Arabidopsis thaliana or Lycopersicon esculentum with Pseudomonas syringae pathovar tomato. Planta, 218(4), 668-672. doi:10.1007/s00425-003-1146-9. [NMR077] MPG.PuRE
3Cheng, Y., Schneider, B., Riese, U., Schubert, B., Li, Z., Hamburger, M. (2004). Farinosones A-C, neurotrophic alkaloidal metabolites from the entomogenous deuteromycete Paecilomyces farinosus. Journal of Natural Products, 67(11), 1854-1858. doi:10.1021/np049761w. [NMR085] MPG.PuRE
4Kuzovkina, I. N., Al'terman, I., Schneider, B. (2004). Specific accumulation and revised structures of acridone alkaloid glucosides in the tips of transformed roots of Ruta graveolens. Phytochemistry, 65(8), 1095-1100. doi:10.1016/j.phytochem.2004.03.003. [NMR081] MPG.PuRE
5Nookandeh, A., Frank, N., Steiner, F., Ellinger, R., Schneider, B., Gerhauser, C., Becker, H. (2004). Xanthohumol metabolites in faeces of rats. Phytochemistry, 65(5), 561-570. doi:10.1016/j.phytochem.2003.11.016. [NMR078] MPG.PuRE
6Oberthur, C., Schneider, B., Graf, H., Hamburger, M. (2004). The elusive indigo precursors in woad (Isatis tinctoria L.) - Identification of the major indigo precursor, isatan A, and a structure revision of isatan B. Chemistry and Biodiversity, 1(1), 174-182. doi:10.1002/cbdv.200490009. [NMR082] MPG.PuRE
7Otálvaro, F., Quinones, W., Echeverri, F., Schneider, B. (2004). Synthesis of [phenyl-13C6]lachnanthocarpone and other 13C-labelled phenylphenalenones. Journal of Labelled Compounds and Radiopharmaceuticals, 47, 147-159. doi:10.1002/jlcr.808. [NMR080] MPG.PuRE
8Schneider, B. (2004). Nuclear magnetic resonance applications to low-molecular metabolites in plant sciences. Progress in Botany, 65(65), 301-322. doi:10.1007/978-3-642-18819-0_12. [NMR083] MPG.PuRE
9Schüler, G., Mithöfer, A., Baldwin, I. T., Berger, S., Ebel, S., Santos, J. G., Herrmann, G., Hölscher, D., Kramell, R., Kutchan, T. M., Maucher, H., Schneider, B., Stenzel, I., Wasternack, C., Boland, W. (2004). Coronalon: a powerful tool in plant stress physiology. FEBS Letters, 563(1-3), 17-22. doi:10.1016/S0014-5793(04)00239-X. [BOL159] OPEN ACCESS gold MPG.PuRE
10Svatos, A., Antonchik, A. P., Schneider, B. (2004). Determination of brassinosteroids in the sub-femtomolar range using dansyl-3-aminophenylboronate derivatization and electrospray mass spectrometry. Rapid Communications in Mass Spectrometry, 18(7), 816-821. doi:10.1002/rcm.1413. [MS042] MPG.PuRE
11Tan, J.-W., Bednarek, P., Liu, J., Schneider, B., Svatos, A., Hahlbrock, K. (2004). Universally occurring phenylpropanoid and species-specific indolic metabolites in infected and uninfected Arabidopsis thaliana roots and leaves. Phytochemistry, 65(6), 691-699. doi:10.1016/j.phytochem.2003.12.009. [NMR079] MPG.PuRE
1Antonchik, A. P., Schneider, B., Zhabinskii, V. N., Konstantinova, O. V., Khripach, V. A. (2003). Biosynthesis of 2,3-epoxybrassinosteroids in seedlings of Secale cereale. Phytochemistry, 63(7), 771-776. doi:10.1016/S0031-9422(03)00354-6. [NMR074] MPG.PuRE
2Baranovsky, A., Schmitt, B., Fowler, D. J., Schneider, B. (2003). Synthesis of new biosynthetically important diarylheptanoids and their oxa- and fluoro-analogues by three different strategies. Synthetic Communications, 33(6), 1019-1045. doi:10.1081/SCC-120016367. [NMR075] MPG.PuRE
3Eckermann, C., Schröder, G., Eckermann, S., Strack, D., Schmidt, E., Schneider, B., Schröder, J. (2003). Stilbenecarboxylate biosynthesis: a new function in the family of chalcone synthase-related proteins. Phytochemistry, 62(3), 271-286. doi:10.1016/s0031-9422(02)00554-x. [NMR068] MPG.PuRE
4Hölscher, D., Williams, D. C., Wildung, M. R., Croteau, R. (2003). A cDNA clone for 3-carene synthase from Salvia stenophylla. Phytochemistry, 62, 1081-1086. doi:10.1016/s0031-9422(02)00674-x. [NMR067] MPG.PuRE
5Opitz, S., Schneider, B. (2003). Oxidative biosynthesis of phenylbenzoisochromenones from phenylphenalenones. Phytochemistry, 62(3), 307-312. doi:10.1016/S0031-9422(02)00546-0. [NMR066] MPG.PuRE
6Opitz, S., Schnitzler, J. P., Hause, B., Schneider, B. (2003). Histochemical analysis of phenylphenalenone-related compounds in Xiphidium caeruleum (Haemodoraceae). Planta, 216(5), 881-889. doi:10.1007/s00425-002-0941-z. [NMR070] MPG.PuRE
7Schneider, B. (2003). Differentiation-dependent levels of benzofuran-type resveratrol dimers in root cultures of Anigozanthos preissii. Phytochemistry, 64(2), 459-462. doi:10.1016/s0031-9422(03)00193-6. [NMR073] MPG.PuRE
8Schneider, B., Gershenzon, J., Graser, G., Hölscher, D., Schmitt, B. (2003). One-dimensional 13C NMR and HPLC-1H NMR techniques for observing carbon-13 and deuterium labelling in biosynthetic studies. Phytochemistry Reviews, 2, 31-43. doi:10.1023/B:PHYT.0000004196.73829.4e. [NMR076] MPG.PuRE
9Scholl, Y., Schneider, B., Dräger, B. (2003). Biosynthesis of calystegines: N-15 NMR and kinetics of formation in root cultures of Calystegia sepium. Phytochemistry, 62(3), 325-332. doi:10.1016/s0031-9422(02)00544-7. [NMR145] MPG.PuRE
1Berlich, M., Menge, S., Bruns, I., Schmidt, J., Schneider, B., Krauss, G.-J. (2002). Coumarins give misleading absorbance with Ellman's reagent suggestive of thiol conjugates. Analyst, 127(3), 333-336. doi:10.1039/b110988j. [NMR063] MPG.PuRE
2Khripach, V. A., Zhabinskii, V. N., Antonchik, A. P., Konstantinova, O. V., Schneider, B. (2002). Synthesis of hexadeuterated 23-dehydroxybrassinosteroids. Steroids, 67(13-14), 1101-1108. doi:10.1016/S0039-128X(02)00071-5. [NMR014] MPG.PuRE
3Khripach, V. A., Zhabinskii, V. N., Konstantinova, O. V., Antonchik, A. P., Schneider, B. (2002). Synthesis of [26-2 H3]brassinosteroids. Steroids, 67(7), 587-595. doi:10.1016/S0039-128X(02)00004-1. [NMR061] MPG.PuRE
4Khripach, V. A., Zhabinskii, V. N., Konstantinova, O. V., Khripach, N. B., Antonchik, A. P., Schneider, B. (2002). [3,3]-Claisen rearrangements in 24 alpha-methyl steroid synthesis - Application to campesterol, crinosterol, and delta(25)-crinosterol side chain construction. Steroids, 67(7), 597-603. doi:10.1016/S0039-128X(02)00007-7. [NMR060] MPG.PuRE
5Opitz, S., Hölscher, D., Oldham, N. J., Bartram, S., Schneider, B. (2002). Phenylphenalenone-related compounds: chemotaxonomic markers of the Haemodoraceae from Xiphidium caeruleum. Journal of Natural Products, 65(8), 1122-1130. doi:10.1021/np020083s. [NMR054] MPG.PuRE
6Opitz, S., Otalvaro, F., Echeverri, F., Quinones, W., Schneider, B. (2002). Isomeric oxabenzochrysenones from Musa acuminata and Wachendorfia thyrsiflora. Natural Product Letters, 16(5), 335-338. doi:10.1080/10575630290033079. [NMR048] MPG.PuRE
7Opitz, S., Schneider, B. (2002). Organ-specific analysis of phenylphenalenone-related compounds in Xiphidium caeruleum. Phytochemistry, 61(7), 819-825. doi:10.1016/S0031-9422(02)00359-X. [NMR056] MPG.PuRE
8Otálvaro, F., Echeverri, F., Quinones, W., Torres, F., Schneider, B. (2002). Correlation between phenylphenalenone phytoalexins and phytopathological properties in Musa and the role of a dihydrophenylphenalene triol. Molecules, 7(3), 331-340. doi:10.3390/70300331. [NMR062] OPEN ACCESS gold MPG.PuRE
9Otálvaro, F., Görls, H., Hölscher, D., Schmitt, B., Echeverri, F., Quinones, W., Schneider, B. (2002). Dimeric phenylphenalenones from Musa acuminata and various Haemodoraceae species. Crystal structure of anigorootin. Phytochemistry, 60(1), 61-66. doi:10.1016/s0031-9422(02)00066-3. [NMR059] MPG.PuRE
10Reichelt, M., Brown, P. D., Schneider, B., Oldham, N. J., Stauber, E. J., Tokuhisa, J. G., Kliebenstein, D. J., Mitchell-Olds, T., Gershenzon, J. (2002). Benzoic acid glucosinolate esters and other glucosinolates from Arabidopsis thaliana. Phytochemistry, 59(6), 663-671. doi:10.1016/S0031-9422(02)00014-6. [MPI020] MPG.PuRE
1Blitzke, T., Baranovsky, A., Schneider, B. (2001). Synthesis and protein binding of (4-carboxybutyl)carbamoyl- substituted taxoids. Helvetica Chimica Acta, 84(7), 1989-1995. doi:10.1002/1522-2675(20010711)84:7<1989:AID-HLCA1989>3.0.CO;2-M. [NMR034] MPG.PuRE
2Gräther, O., Schneider, B. (2001). The metabolic diversity of plant cell and tissue cultures. In Progress in Botany (pp. 266-304). Berlin: Springer-Verlag. [NMR032] MPG.PuRE
3Hagemeier, J., Schneider, B., Oldham, N. J., Hahlbrock, K. (2001). Accumulation of soluble and wall-bound indolic metabolites in Arabidopsis thaliana leaves infected with virulent or avirulent Pseudomonas syringae pathovar tomato strains. Proceedings of the National Academy of Sciences of the United States of America, 98(2), 753-758. doi:10.1073/pnas.021551098. [MPI009] OPEN ACCESS gold MPG.PuRE
4Konstantinova, O. V., Antonchik, A. P., Oldham, N. J., Zhabinskii, V. N., Khripach, V. A., Schneider, B. (2001). Analysis of underivatized brassinosteroids by HPLC/APCI-MS. Occurrence of 3-epibrassinolide in Arabidopsis thaliana. Collection of Czechoslovak Chemical Communications, 66(12), 1729-1734. doi:10.1135/cccc20011729. [MPI021] MPG.PuRE
5Schmitt, B., Schneider, B. (2001). Phenylpropanoid interconversion in Anigozanthos preissii observed by high-performance liquid chromatography-nuclear magnetic resonance spectroscopy. Phytochemical Analysis, 12(1), 43-47. doi:10.1002/1099-1565(200101/02)12:1<43:AID-PCA546>3.0.CO;2-Z. [NMR030] MPG.PuRE
6Schmitt, B., Schneider, B. (2001). Use of stable isotope labelling in biosynthetic studies on phenylphenalenones. In U. Pleiss, R. Veges (Eds.), Synthesis and Applications of Isotopically Labelled Compounds: Proceedings of the Seventh International Symposium, Dresden, Germany, 18-22 June 2000 (pp. 640-643). Chichester: Wiley. [NMR033] MPG.PuRE
7Schneider, B. (2001). Analogies in the conversion of natural and synthetic substrates in plants revealed by labelling studies. In U. Pleiss, R. Veges (Eds.), Synthesis and Applications of Isotopically Labelled Compounds: Proceedings of the Seventh International Symposium, Dresden, Germany, 18-22 June 2000 (pp. 597-599). Chichester: Wiley. [NMR035] MPG.PuRE
8Schneider, B. (2001). Pathways and enzymes of brassinosteroid biosynthesis. In Progress in Botany (pp. 286-306). Berlin: Springer-Verlag. [NMR052] MPG.PuRE
9Sicker, D., Schneider, B., Hennig, L., Knop, M., Schulz, M. (2001). Correction to: Glycoside carbamates from benzoxazolin-2(3H)-one detoxification in extracts and exudates of corn roots (2001: 58, 819-825). Phytochemistry, 58, 819-825. doi:10.1016/S0031-9422(01)00299-0. [NMR053] MPG.PuRE
10Stündl, U., Schneider, B. (2001). 3 beta-Brassinosteroid dehydrogenase activity in Arabidopsis and tomato. Phytochemistry, 58(7), 989-994. doi:10.1016/s0031-9422(01)00387-9. [NMR064] MPG.PuRE
1Graser, G., Schneider, B., Oldham, N. J., Gershenzon, J. (2000). The methionine chain elongation pathway in the biosynthesis of glucosinolates in Eruca sativa (Brassicaceae). Archives of Biochemistry and Biophysics, 378(2), 411-419. doi:10.1006/abbi.2000.1812. [MPI008] MPG.PuRE
2Hölscher, D., Schneider, B. (2000). Phenalenones from Strelitzia reginae. Journal of Natural Products, 63(7), 1027-1028. doi:10.1021/np000035c. [NMR058] MPG.PuRE
3Schmitt, B., Hölscher, D., Schneider, B. (2000). Variability of phenylpropanoid precursors in the biosynthesis of phenylphenalenones in Anigozanthos preissii. Phytochemistry, 53(3), 331-337. doi:10.1016/s0031-9422(99)00544-0. [NMR031] MPG.PuRE
4Schneider, B. (2000). Natural products: Liquid chromatography - Nuclear Magnetic Resonance. In I. D. Wilson, T. R. Adlard, M. Cooke, C. F. Poole (Eds.), Encyclopedia of Separation Science (pp. 3434-3445). London: Academic Press. [NMR057] MPG.PuRE
1Adam, G., Schmidt, J., Schneider, B. (1999). Brassinosteroids. Progress in the Chemistry of Organic Natural Products, 78, 1-46. [NMR050] MPG.PuRE
2Adam, G., Schneider, B. (1999). Uptake, transport and metabolism. In A. Sakurai, T. Yokota, S. D. Clouse (Eds.), Brassinosteroids: Steroidal Plant Hormones (pp. 113-136). Tokyo: Springer. [NMR001] MPG.PuRE
3Fowler, D. J., Hamilton, J. T. G., Humphrey, A. J., O'Hagan, D. (1999). Plant terpene biosynthesis. The biosynthesis of linalyl acetate in Mentha citrata. Tetrahedron Letters, 40(19), 3803-3806. doi:10.1016/S0040-4039(99)00532-8. [NMR071] MPG.PuRE
4Hartung, C., Illgen, K., Sieler, J., Schneider, B., Schulze, B. (1999). Synthesis of stable cyclic sulfinamides with a hydroperoxy function by oxidation of isothiazolium salts. Helvetica Chimica Acta, 82(5), 685-695. doi:10.1002/(SICI)1522-2675(19990505)82:5<685:AID-HLCA685>3.0.CO;2-4. [NMR006] MPG.PuRE
5Hölscher, D., Schneider, B. (1999). HPLC-NMR analysis of phenylphenalenones and a stilbene from Anigozanthos flavidus. Phytochemistry, 50(1), 155-161. doi:10.1016/S0031-9422(98)00495-6. [NMR004] MPG.PuRE
6Kolbe, A., Krauss, G., Schneider, B. (1999). Ornithopus sativus Brot. (Serradella): in vitro culture, phytochemical studies, and biotransformation. In Y. P. S. Bajaj (Ed.), Medicinal and Aromatic Plants XI. Biotechnology in Agriculture and Forestry (pp. 310-323). Berlin, Heidelberg: Springer. [NMR007] MPG.PuRE
7Kolbe, A., Krauss, G., Schneider, B. (1999). Ornithopus sativus Brot. (Serradella): in vitro culture, phytochemical studies, and biotransformation. In Y. P. S. Bajaj (Ed.), Medicinal and aromatic plants XI (pp. 310-323). Berlin: Springer. [NMR047] MPG.PuRE
8Mantrova, O. V., Dunaeva, M. V., Kuzovkina, I. N., Schneider, B., Muller-Uri, F. (1999). Effect of methyl jasmonate on anthraquinone biosynthesis in transformed madder roots. Russian Journal of Plant Physiology, 46(2), 248-251. [NMR029] MPG.PuRE
9Röhl, I., Schneider, B., Schmidt, B., Zeeck, E. (1999). L-Ovothiol A: The egg release pheromone of the marine polychaete Platynereis dumerilii: Annelida: Polychaeta. Zeitschrift für Naturforschung, C: Journal of Biosciences, 54(12), 1145-1147. doi:10.1515/znc-1999-1222. [NMR069] MPG.PuRE
10Schmitt, B., Schneider, B. (1999). Dihydrocinnamic acids are involved in the biosynthesis of phenylphenalenones in Anigozanthos preissii. Phytochemistry, 52(2), 45-53. doi:10.1016/S0031-9422(99)00116-8. [NMR002] MPG.PuRE
11Schneider, B. (1999). Brassinosteroid metabolism. Chemicke Listy, 93(1), 12-14. [NMR016] OPEN ACCESS gold MPG.PuRE
12Schupp, P., Eder, C., Proksch, P., Wray, V., Schneider, B., Herderich, M., Paul, V. (1999). Staurosporine derivatives from the ascidian Eudistoma toealensis and its predatory flatworm Pseudoceros sp. Journal of Natural Products, 62(7), 959-962. doi:10.1021/np980527d. [NMR011] MPG.PuRE
13Winter, J., Schneider, B., Meyenburg, S., Strack, D., Adam, G. (1999). Monitoring brassinosteroid biosynthetic enzymes by fluorescent tagging and HPLC analysis of their substrates and products. Phytochemistry, 51(2), 237-242. doi:10.1016/S0031-9422(98)00760-2. [NMR003] MPG.PuRE
14Zhao, Y., Nookandeh, A., Schneider, B., Sun, X. F., Schmitt, B., Stöckigt, J. (1999). Lignans from Torreya jackii identified by stopped-flow high- performance liquid chromatography nuclear magnetic resonance spectroscopy. Journal of Chromatography A, 837(1-2), 83-91. doi:10.1016/S0021-9673(99)00050-3. [NMR005] MPG.PuRE
1Hölscher, D., Schneider, B. (1998). Phenylphenalenones from Ensete ventricosum. Phytochemistry, 49(7), 2155-2157. doi:10.1016/S0031-9422(98)00423-3. [NMR008] MPG.PuRE
2Kolbe, A., Schneider, B., Porzel, A., Adam, G. (1998). Metabolic inversion of the 3-hydroxy function of brassinosteroids. Phytochemistry, 48(3), 467-470. doi:10.1016/S0031-9422(98)00037-5. [NMR009] MPG.PuRE
3Kolbe, A., Schneider, B., Voigt, B., Adam, G. (1998). Labelling of biogenetic brassinosteroid precursors. Journal of Labelled Compounds and Radiopharmaceuticals, 41(2), 131-137. doi:10.1002/(SICI)1099-1344(199802)41:2<131:AID-JLCR59>3.0.CO;2-F. [NMR026] MPG.PuRE
4Krause, U., Schneider, B. (1998). Investigations on the phenylpropane biosynthesis in in vitro cultures of Zingiberaceae spp. In P. Schreier, M. Herderich, H.-U. Humpf, W. Schwab (Eds.), Natural Product Analysis (pp. 393-394). Braunschweig/Wiesbaden: Vieweg. [NMR045] MPG.PuRE
5Maier, W., Schneider, B., Strack, D. (1998). Biosynthesis of sesquiterpenoid cyclohexenone derivatives in mycorrhizal barley roots proceeds via the glyceraldehyde 3- phosphate/pyruvate pathway. Tetrahedron Letters, 39(7), 521-524. doi:10.1016/S0040-4039(97)10673-6. [NMR027] MPG.PuRE
6Opitz, S., Koehler, G., Mabelis, A. (1998). Local movement of the grasshopper Chorthippus parallelus (Zett.). In M. J. Sommeijer, P. J. Francke (Eds.), Proceedings of the Section Experimental and Applied Entomology of the Netherlands Entomological Society (N.E.V.) (pp. 53-58). Netherlands Entomological Society, Plantage Middenlaan 64, 1018 DH Amsterdam 414, Netherlands. [GER073] MPG.PuRE
7Opitz, S., Köhler, G., Mabelis, A. (1998). Grasshopper movement in a Dutch heathland - Chorthippus parallelus (Zett.). Proceedings of the Section Experimental and Applied Entomology of the Netherlands Entomological Society, 9, 53-58. [GER082] MPG.PuRE
8Porzel, A., Hai, T., Kolbe, A., Schneider, B., Adam, G. (1998). Structure elucidation of brassinosteroid metabolites by NMR spectroscopy. In P. Schreier (Ed.), Natural Product Analysis (pp. 135-136). Braunschweig/Wiesbaden: Vieweg. [NMR046] MPG.PuRE
9Schmitt, B., Schneider, B. (1998). NMR-Spectroscopic investigations on the dynamics of phenylpropane biosynthetic pathways in Anigozanthos preissii. In P. Schreier (Ed.), Natural Product Analysis (pp. 127-128). Braunschweig/Wiesbaden: Vieweg. [NMR044] MPG.PuRE
10Schneider, B., Hölscher, D., Kolbe, A., Blitzke, T. (1998). HPLC-NMR in phytochemical analysis. In P. Schreier (Ed.), Natural Product Analysis (pp. 137-142). Braunschweig/Wiesbaden: Vieweg. [NMR043] MPG.PuRE
11Schneider, B., Zhao, Y., Blitzke, T., Schmitt, B., Nookandeh, A., Sun, X. F., Stockigt, J. (1998). Taxane analysis by high performance liquid chromatography nuclear magnetic resonance spectroscopy of Taxus species. Phytochemical Analysis, 9(5), 237-244. doi:10.1002/(SICI)1099-1565(199809/10)9:5<237:AID-PCA411>3.0.CO;2-U. [NMR010] MPG.PuRE
12Wieland, I., Kluge, M., Schneider, B., Schmidt, J., Sicker, D., Schulz, M. (1998). 3-beta-D-glucopyranosyl-benzoxazolin-2(3H)-one—A detoxification product of benzoxazolin-2(3H)-one in oat roots. Phytochemistry, 49(3), 719-722. doi:10.1016/S0031-9422(97)91012-8. [NMR028] MPG.PuRE
1Hölscher, D., Schneider, B. (1997). Phenylphenalenones from root cultures of Anigozanthos preissii. Phytochemistry, 45(1), 87-91. doi:10.1016/S0031-9422(96)00679-6. [NMR023] MPG.PuRE
2Kluge, M., Schneider, B., Sicker, D. (1997). Diastereoselective synthesis of the benzoxazinone acetal glucoside ent-GDIMBOA: the first enantiomer of a natural acetal glucoside. Carbohydrate Research, 298(3), 147-152. doi:10.1016/S0008-6215(96)00303-5. [NMR022] MPG.PuRE
3Kolbe, A., Porzel, A., Schneider, B., Adam, G. (1997). Diglycosidic metabolites of 24-epi-teasterone in cell suspension cultures of Lycopersicon esculentum L. Phytochemistry, 46(6), 1019-1022. doi:10.1016/S0031-9422(97)00390-7. [NMR025] MPG.PuRE
4Schneider, B. (1997). In-vivo nuclear magnetic resonance spectroscopy of low-molecular-weight compounds in plant cells. Planta, 203(1), 1-8. doi:10.1007/s00050158. [NMR036] MPG.PuRE
5Schneider, B., Kolbe, A., Winter, J., Porzel, A., Schmidt, J., Strack, D., Adam, G. (1997). Pathways and enzymology of brassinosteroid metabolism. In Proceedings of the Plant Growth Regulator Society of America, 24. Annual Meeting. [NMR042] MPG.PuRE
6Winter, J., Schneider, B., Strack, D., Adam, G. (1997). Role of a cytochrome P450-dependent monooxygenase in the hydroxylation of 24-epi-brassinolide. Phytochemistry, 45(2), 233-237. doi:10.1016/S0031-9422(96)00827-8. [NMR024] MPG.PuRE