| Year |
Citation |
Score |
| 2020 |
Scognamiglio M, Schneider B. Identification of Potential Allelochemicals From Donor Plants and Their Synergistic Effects on the Metabolome of . Frontiers in Plant Science. 11: 1046. PMID 32849675 DOI: 10.3389/Fpls.2020.01046 |
0.335 |
|
| 2020 |
Dudek B, Schneider B, Hilger HH, Stavenga DG, Martínez-Harms J. Highly different flavonol content explains geographic variations in the UV reflecting properties of flowers of the corn poppy, Papaver rhoeas (Papaveraceae). Phytochemistry. 178: 112457. PMID 32692661 DOI: 10.1016/J.Phytochem.2020.112457 |
0.335 |
|
| 2019 |
Désiré S, Ernestine N, Bruno TB, Lazare SS, Ulrich DD, Lateef M, Schneider B, Ali MS, Barthélemy N. A new dammarane type triterpene glucoside from the aerial parts of (Rhamnaceae). Natural Product Research. 1-12. PMID 31782674 DOI: 10.1080/14786419.2019.1690483 |
0.344 |
|
| 2019 |
Hadavand Mirzaei H, Firuzi O, Chandran JN, Schneider B, Jassbi AR. 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 |
0.345 |
|
| 2018 |
Chen Y, Paetz C, Schneider B. Organ-specific distribution and non-enzymatic conversions indicate a metabolic network of phenylphenalenones in Xiphidium caeruleum. Phytochemistry. 159: 30-38. PMID 30572115 DOI: 10.1016/J.Phytochem.2018.12.004 |
0.379 |
|
| 2018 |
Dudek B, Schnurrer F, Dahse HM, Paetz C, Warskulat AC, Weigel C, Voigt K, Schneider B. Formation of Nudicaulins In Vivo and In Vitro and the Biomimetic Synthesis and Bioactivity of -Methylated Nudicaulin Derivatives. Molecules (Basel, Switzerland). 23. PMID 30567384 DOI: 10.3390/Molecules23123357 |
0.374 |
|
| 2018 |
Krieger C, Roselli S, Kellner-Thielmann S, Galati G, Schneider B, Grosjean J, Olry A, Ritchie D, Matern U, Bourgaud F, Hehn A. The CYP71AZ P450 Subfamily: A Driving Factor for the Diversification of Coumarin Biosynthesis in Apiaceous Plants. Frontiers in Plant Science. 9: 820. PMID 29971079 DOI: 10.3389/Fpls.2018.00820 |
0.308 |
|
| 2018 |
Martinez-Harms J, Warskulat AC, Dudek B, Kunert G, Lorenz S, Hansson BS, Schneider B. Biosynthetic and functional color-scent associations in flowers of Papaver nudicaule and its impact on pollinators. Chembiochem : a European Journal of Chemical Biology. PMID 29696753 DOI: 10.1002/Cbic.201800155 |
0.304 |
|
| 2018 |
Feistel F, Paetz C, Menezes RC, Veit D, Schneider B. ACYLATED QUINIC ACIDS ARE THE MAIN SALICORTIN METABOLITES IN THE LEPIDOPTERAN SPECIALIST HERBIVORE Cerura vinula. Journal of Chemical Ecology. PMID 29549572 DOI: 10.1007/S10886-018-0945-1 |
0.356 |
|
| 2018 |
Chen Y, Paetz C, Schneider B. Precursor-Directed Biosynthesis of Phenylbenzoisoquinolindione Alkaloids and the Discovery of a Phenylphenalenone-Based Plant Defense Mechanism. Journal of Natural Products. PMID 29509420 DOI: 10.1021/Acs.Jnatprod.7B00885 |
0.382 |
|
| 2018 |
Naseri M, Emami SA, Asili J, Tayarani-Najaran Z, Dehghan G, Schneider B, Iranshahi M. Rupestrines A-D, alkaloids from the aerial parts of Corydalis rupestris. Bioorganic Chemistry. 77: 651-659. PMID 29502026 DOI: 10.1016/J.Bioorg.2018.02.019 |
0.305 |
|
| 2018 |
Carqueijeiro I, Dugé de Bernonville T, Lanoue A, Dang TT, 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, et al. 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 : For Cell and Molecular Biology. PMID 29438577 DOI: 10.1111/Tpj.13868 |
0.57 |
|
| 2018 |
Stavrinides A, Tatsis E, Dang TT, Caputi L, Stevenson C, Lawson D, Schneider B, O'Connor S. Discovery of a short chain dehydrogenase from Catharanthus roseus that produces a novel monoterpene indole alkaloid. Chembiochem : a European Journal of Chemical Biology. PMID 29424954 DOI: 10.1002/Cbic.201700621 |
0.784 |
|
| 2017 |
Soltani S, Amin GR, Salehi-Sourmaghi MH, Schneider B, Lorenz S, Iranshahi M. Sulfur-containing compounds from the roots of Ferula latisecta and their cytotoxic activities. Fitoterapia. PMID 29066298 DOI: 10.1016/J.Fitote.2017.10.012 |
0.344 |
|
| 2017 |
Feistel F, Paetz C, Lorenz S, Beran F, Kunert G, Schneider B. Idesia polycarpa (Salicaceae) leaf constituents and their toxic effect on Cerura vinula and Lymantria dispar (Lepidoptera) larvae. Phytochemistry. 143: 170-179. PMID 28822319 DOI: 10.1016/J.Phytochem.2017.08.008 |
0.339 |
|
| 2017 |
Mageroy MH, Jancsik S, Yuen MMS, Fischer M, Withers SG, Paetz C, Schneider B, MacKay JJ, Bohlmann J. A conifer UDP-sugar dependent glycosyltransferase contributes to acetophenone metabolism and defense against insects. Plant Physiology. PMID 28794260 DOI: 10.1104/Pp.17.00611 |
0.354 |
|
| 2017 |
Ospina F, Ramirez A, Cano M, Hidalgo W, Schneider B, Otálvaro F. Synthesis of Positional Isomeric Phenylphenalenones. The Journal of Organic Chemistry. PMID 28345339 DOI: 10.1021/Acs.Joc.6B02985 |
0.31 |
|
| 2017 |
Brkljača R, Schneider B, Hidalgo W, Otálvaro F, Ospina F, Lee S, Hoshino M, Fujita M, Urban S. Application of the Crystalline Sponge Method to Revise the Structure of the Phenalenone Fuliginone. Molecules (Basel, Switzerland). 22. PMID 28146104 DOI: 10.3390/Molecules22020211 |
0.361 |
|
| 2017 |
Ramsay A, Fliniaux O, Quéro A, Molinié R, Demailly H, Hano C, Paetz C, Roscher A, Grand E, Kovensky J, Schneider B, Mesnard F. Kinetics of the incorporation of the main phenolic compounds into the lignan macromolecule during flaxseed development. Food Chemistry. 217: 1-8. PMID 27664601 DOI: 10.1016/J.Foodchem.2016.08.039 |
0.311 |
|
| 2017 |
Ocampos FMM, Paetz C, Antar GM, Menezes RC, Miguel OG, Schneider B. Phytochemical profile of Schiekia orinocensis (Haemodoraceae) Phytochemistry Letters. 21: 139-145. DOI: 10.1016/J.Phytol.2017.06.008 |
0.387 |
|
| 2017 |
Schneider B. 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 |
0.352 |
|
| 2017 |
Hadavand Mirzaei H, Firuzi O, Schneider B, Baldwin IT, Jassbi AR. Cytotoxic diterpenoids from the roots of Salvia lachnocalyx Revista Brasileira De Farmacognosia. 27: 475-479. DOI: 10.1016/J.Bjp.2017.01.009 |
0.35 |
|
| 2016 |
Hölscher D, Vollrath A, Kai M, Dhakshinamoorthy S, Menezes RC, Svatoš A, Schubert US, Buerkert A, Schneider B. Local phytochemical response of Musa acuminata × balbisiana Colla cv. 'Bluggoe' (ABB) to colonization by Sternorrhyncha. Phytochemistry. PMID 27839785 DOI: 10.1016/J.Phytochem.2016.10.007 |
0.313 |
|
| 2016 |
Chen Y, Paetz C, Menezes RC, Schneider B. Cultured roots of Xiphidium caeruleum: Phenylphenalenones and their biosynthetic and extractant-dependent conversion. Phytochemistry. PMID 27816177 DOI: 10.1016/J.Phytochem.2016.10.011 |
0.377 |
|
| 2016 |
Handrick V, Robert CA, Ahern KR, Zhou S, Machado RA, Maag D, Glauser G, Fernandez-Penny FE, Chandran JN, Rodgers-Melnik E, Schneider B, Buckler ES, Boland W, Gershenzon J, Jander G, et al. Biosynthesis of 8-O-Methylated Benzoxazinoid Defense Compounds in Maize. The Plant Cell. 28: 1682-700. PMID 27317675 DOI: 10.1105/Tpc.16.00065 |
0.336 |
|
| 2016 |
Jassbi AR, Eghtesadi F, Hazeri N, Ma'sumi H, Valizadeh J, Chandran JN, Schneider B, Baldwin IT. The roots of Salvia rhytidea: a rich source of biologically active diterpenoids. Natural Product Research. 1-5. PMID 27266560 DOI: 10.1080/14786419.2016.1188096 |
0.39 |
|
| 2016 |
Chen Y, Paetz C, Menezes RC, Schneider B. Phenylbenzoisoquinolindione alkaloids accumulate in stamens of Xiphidium caeruleum Aubl. flowers. Phytochemistry. PMID 27179683 DOI: 10.1016/J.Phytochem.2016.05.002 |
0.39 |
|
| 2016 |
Liu Y, Luo SH, Schmidt A, Gershenzon J, Wang G, Sun GL, Grant M, Kuang C, Yang MJ, Jing SX, Li CH, Schneider B, Li SH. A geranylfarnesyl diphosphate synthase provides the precursor for sesterterpenoid (C25) formation in the glandular trichomes of Leucosceptrum canum. The Plant Cell. PMID 26941091 DOI: 10.1105/Tpc.15.00715 |
0.375 |
|
| 2016 |
Jassbi AR, Firuzi O, Miri R, Salhei S, Zare S, Zare M, Masroorbabanari M, Chandran JN, Schneider B, Baldwin IT. Cytotoxic activity and chemical constituents of Anthemis mirheydari. Pharmaceutical Biology. 1-6. PMID 26864903 DOI: 10.3109/13880209.2016.1141220 |
0.325 |
|
| 2016 |
Ospina F, Hidalgo W, Cano M, Schneider B, Otálvaro F. Synthesis of 8-Phenylphenalenones: 2-Hydroxy-8-(4-hydroxyphenyl)-1H-phenalen-1-one from Eichhornia crassipes. The Journal of Organic Chemistry. PMID 26741281 DOI: 10.1021/Acs.Joc.5B02559 |
0.302 |
|
| 2016 |
Hidalgo W, Chandran JN, Menezes RC, Otálvaro F, Schneider B. Phenylphenalenones protect banana plants from infection by Mycosphaerella fijiensis and are deactivated by metabolic conversion. Plant, Cell & Environment. 39: 492-513. PMID 26290378 DOI: 10.1111/Pce.12630 |
0.358 |
|
| 2015 |
Schneider B, Warskulat AC, Tatsis EC, Dudek B, Kai M, Lorenz S. An unprecedented utilization of pelargonidin and indole for the biosynthesis of plant indole alkaloids. Chembiochem : a European Journal of Chemical Biology. PMID 26670055 DOI: 10.1002/Cbic.201500572 |
0.754 |
|
| 2015 |
Iranshahy M, Tayarani-Najaran Z, Kasaian J, Ghandadi M, Emami SA, Asili J, Chandran JN, Schneider B, Iranshahi M. 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 : Ptr. PMID 26581585 DOI: 10.1002/Ptr.5519 |
0.319 |
|
| 2015 |
Boachon B, Junker RR, Miesch L, Bassard JE, Höfer R, Caillieaudeaux R, Seidel DE, Lesot A, Heinrich C, Ginglinger JF, Allouche L, Vincent B, Wahyuni DS, Paetz C, Beran F, ... ... Schneider B, et al. 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: 2972-90. PMID 26475865 DOI: 10.1105/Tpc.15.00399 |
0.327 |
|
| 2015 |
Baranovsky AV, Bolibrukh DA, Schneider B. Solvolysis of 14,17-etheno-bridged 16α-nitroestratrienyl acetate and lactam formation pathways studied by LC-NMR and LC-MS. Structures of minor products. Steroids. 104: 37-48. PMID 26296334 DOI: 10.1016/J.Steroids.2015.08.009 |
0.322 |
|
| 2015 |
Hidalgo W, Kai M, Schneider B. 4-Methoxycinnamic acid--An unusual phenylpropanoid involved in phenylphenalenone biosynthesis in Anigozanthos preissii. Phytochemistry. 117: 476-481. PMID 26218676 DOI: 10.1016/J.Phytochem.2015.07.017 |
0.349 |
|
| 2015 |
Hidalgo W, Cano M, Arbelaez M, Zarrazola E, Gil J, Schneider B, Otálvaro F. 4-Phenylphenalenones as a template for new photodynamic compounds against Mycosphaerella fijiensis. Pest Management Science. PMID 26058960 DOI: 10.1002/Ps.4055 |
0.301 |
|
| 2015 |
Lu X, Dittgen J, Piślewska-Bednarek M, Molina A, Schneider B, Svatoš A, Doubský J, Schneeberger K, Weigel D, Bednarek P, Schulze-Lefert P. Mutant Allele-Specific Uncoupling of PENETRATION3 Functions Reveals Engagement of the ATP-Binding Cassette Transporter in Distinct Tryptophan Metabolic Pathways. Plant Physiology. 168: 814-27. PMID 26023163 DOI: 10.1104/Pp.15.00182 |
0.322 |
|
| 2015 |
Hölscher D, Fuchser J, Knop K, Menezes RC, Buerkert A, Svatoš A, Schubert US, Schneider B. 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: 239-45. PMID 26004822 DOI: 10.1016/J.Phytochem.2015.04.010 |
0.354 |
|
| 2015 |
Feistel F, Paetz C, Lorenz S, Schneider B. The absolute configuration of salicortin, HCH-salicortin and tremulacin from Populus trichocarpa × deltoides Beaupré. Molecules (Basel, Switzerland). 20: 5566-73. PMID 25830788 DOI: 10.3390/Molecules20045566 |
0.347 |
|
| 2015 |
Huber M, Triebwasser-Freese D, Reichelt M, Heiling S, Paetz C, Chandran JN, Bartram S, Schneider B, Gershenzon J, Erb M. Identification, quantification, spatiotemporal distribution and genetic variation of major latex secondary metabolites in the common dandelion (Taraxacum officinale agg.). Phytochemistry. 115: 89-98. PMID 25682510 DOI: 10.1016/J.Phytochem.2015.01.003 |
0.378 |
|
| 2015 |
Chitsazian-Yazdi M, Agnolet S, Lorenz S, Schneider B, Es'haghi Z, Kasaian J, Khameneh B, Iranshahi M. Foetithiophenes C-F, thiophene derivatives from the roots of Ferula foetida. Pharmaceutical Biology. 53: 710-4. PMID 25430396 DOI: 10.3109/13880209.2014.939765 |
0.316 |
|
| 2015 |
Shokoohinia Y, Sajjadi S, Jassbi AR, Moradi H, Ghassemi N, Schneider B. Sesquiterpenes and Flavonoids of Anthemis odontostephana var. odontostephana Chemistry of Natural Compounds. 51: 491-494. DOI: 10.1007/S10600-015-1322-8 |
0.365 |
|
| 2014 |
Kia SH, Schulz M, Ayah E, Schouten A, Müllenborn C, Paetz C, Schneider B, Hofmann D, Disko U, Tabaglio V, Marocco A. Abutilon theophrasti's defense against the allelochemical benzoxazolin-2(3H)-one: support by Actinomucor elegans. Journal of Chemical Ecology. 40: 1286-98. PMID 25432667 DOI: 10.1007/S10886-014-0529-7 |
0.377 |
|
| 2014 |
Tatsis EC, Eylert E, Maddula RK, Ostrozhenkova E, Svatoš A, Eisenreich W, Schneider B. Biosynthesis of Nudicaulins: A (13) CO2 -pulse/chase labeling study with Papaver nudicaule. Chembiochem : a European Journal of Chemical Biology. 15: 1645-50. PMID 24919663 DOI: 10.1002/Cbic.201402109 |
0.744 |
|
| 2014 |
Monakhova Y, Schneider B. The intramolecular Diels-Alder reaction of diarylheptanoids--quantum chemical calculation of structural features favoring the formation of phenylphenalenones. Molecules (Basel, Switzerland). 19: 5231-42. PMID 24762963 DOI: 10.3390/Molecules19045231 |
0.361 |
|
| 2014 |
Hölscher D, Dhakshinamoorthy S, Alexandrov T, Becker M, Bretschneider T, Buerkert A, Crecelius AC, De Waele D, Elsen A, Heckel DG, Heklau H, Hertweck C, Kai M, Knop K, Krafft C, ... ... Schneider B, et al. 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: 105-10. PMID 24324151 DOI: 10.1073/Pnas.1314168110 |
0.345 |
|
| 2014 |
Fang J, Schneider B. Laser microdissection: a sample preparation technique for plant micrometabolic profiling. Phytochemical Analysis : Pca. 25: 307-13. PMID 24108508 DOI: 10.1002/Pca.2477 |
0.314 |
|
| 2014 |
Ramsay A, Fliniaux O, Fang J, Molinie R, Roscher A, Grand E, Guillot X, Kovensky J, Fliniaux MA, Schneider B, Mesnard F. Development of an NMR metabolomics-based tool for selection of flaxseed varieties Metabolomics. 10: 1258-1267. DOI: 10.1007/S11306-014-0664-8 |
0.304 |
|
| 2013 |
Ginglinger JF, Boachon B, Höfer R, Paetz C, Köllner TG, Miesch L, Lugan R, Baltenweck R, Mutterer J, Ullmann P, Beran F, Claudel P, Verstappen F, Fischer MJ, Karst F, ... ... Schneider B, et al. Gene coexpression analysis reveals complex metabolism of the monoterpene alcohol linalool in Arabidopsis flowers. The Plant Cell. 25: 4640-57. PMID 24285789 DOI: 10.1105/Tpc.113.117382 |
0.306 |
|
| 2013 |
Irmisch S, McCormick AC, Boeckler GA, Schmidt A, Reichelt M, Schneider B, Block K, Schnitzler JP, Gershenzon J, Unsicker SB, Köllner TG. Two herbivore-induced cytochrome P450 enzymes CYP79D6 and CYP79D7 catalyze the formation of volatile aldoximes involved in poplar defense. The Plant Cell. 25: 4737-54. PMID 24220631 DOI: 10.1105/Tpc.113.118265 |
0.345 |
|
| 2013 |
Besseau S, Kellner F, Lanoue A, Thamm AMK, Salim V, Schneider B, Geu-Flores F, Höfer R, Guirimand G, Guihur A, Oudin A, Glevarec G, Foureau E, Papon N, Clastre M, et al. A pair of tabersonine 16-hydroxylases initiates the synthesis of vindoline in an organ-dependent manner in Catharanthus roseus Plant Physiology. 163: 1792-1803. PMID 24108213 DOI: 10.1104/Pp.113.222828 |
0.549 |
|
| 2013 |
Duque L, Zapata C, Rojano B, Schneider B, Otálvaro F. Radical scavenging capacity of 2,4-dihydroxy-9-phenyl-1H-phenalen-1-one: a functional group exclusion approach. Organic Letters. 15: 3542-5. PMID 23834597 DOI: 10.1021/Ol400384Z |
0.31 |
|
| 2013 |
Hammerbacher A, Schmidt A, Wadke N, Wright LP, Schneider B, Bohlmann J, Brand WA, Fenning TM, Gershenzon J, Paetz C. A common fungal associate of the spruce bark beetle metabolizes the stilbene defenses of Norway spruce. Plant Physiology. 162: 1324-36. PMID 23729780 DOI: 10.1104/Pp.113.218610 |
0.35 |
|
| 2013 |
Tatsis EC, Böhm H, Schneider B. Occurrence of nudicaulin structural variants in flowers of papaveraceous species. Phytochemistry. 92: 105-12. PMID 23684236 DOI: 10.1016/J.Phytochem.2013.04.011 |
0.732 |
|
| 2013 |
Miosic S, Knop K, Hölscher D, Greiner J, Gosch C, Thill J, Kai M, Shrestha BK, Schneider B, Crecelius AC, Schubert US, Svatoš A, Stich K, Halbwirth H. 4-Deoxyaurone formation in Bidens ferulifolia (Jacq.) DC. Plos One. 8: e61766. PMID 23667445 DOI: 10.1371/Journal.Pone.0061766 |
0.348 |
|
| 2013 |
de Souza GD, Mithöfer A, Daolio C, Schneider B, Rodrigues-Filho E. Identification of Alternaria alternata mycotoxins by LC-SPE-NMR and their cytotoxic effects to soybean (Glycine max) cell suspension culture. Molecules (Basel, Switzerland). 18: 2528-38. PMID 23442929 DOI: 10.3390/Molecules18032528 |
0.342 |
|
| 2013 |
Kunert M, Rahfeld P, Shaker KH, Schneider B, David A, Dettner K, Pasteels JM, Boland W. Beetles do it differently: two stereodivergent cyclisation modes in iridoid-producing leaf-beetle larvae. Chembiochem : a European Journal of Chemical Biology. 14: 353-60. PMID 23341265 DOI: 10.1002/Cbic.201200689 |
0.305 |
|
| 2013 |
Happyana N, Agnolet S, Muntendam R, Van Dam A, Schneider B, Kayser O. Analysis of cannabinoids in laser-microdissected trichomes of medicinal Cannabis sativa using LCMS and cryogenic NMR Phytochemistry. 87: 51-59. PMID 23280038 DOI: 10.1016/J.Phytochem.2012.11.001 |
0.352 |
|
| 2013 |
Baranovsky AV, Bolibrukh DA, Khripach VA, Schneider B. Diels-Alder reaction of androsta-14,16-dien-17-yl acetates with nitroethylene: product distribution and selected adduct transformations. Steroids. 78: 282-7. PMID 23261956 DOI: 10.1016/J.Steroids.2012.11.015 |
0.563 |
|
| 2013 |
Tatsis EC, Schaumlöffel A, Warskulat AC, Massiot G, Schneider B, Bringmann G. Nudicaulins, yellow flower pigments of Papaver nudicaule: revised constitution and assignment of absolute configuration. Organic Letters. 15: 156-9. PMID 23249326 DOI: 10.1021/Ol303211W |
0.709 |
|
| 2013 |
Fang J, Ramsay A, Paetz C, Tatsis EC, Renouard S, Hano C, Grand E, Fliniaux O, Roscher A, Mesnard F, Schneider B. Concentration kinetics of secoisolariciresinol diglucoside and its biosynthetic precursor coniferin in developing flaxseed Phytochemical Analysis. 24: 41-46. PMID 22689568 DOI: 10.1002/Pca.2377 |
0.714 |
|
| 2013 |
Munde T, Brand S, Hidalgo W, Maddula RK, Svatoš A, Schneider B. Biosynthesis of tetraoxygenated phenylphenalenones in Wachendorfia thyrsiflora. Phytochemistry. 91: 165-76. PMID 22429758 DOI: 10.1016/J.Phytochem.2012.02.020 |
0.307 |
|
| 2013 |
Soh D, Nkwengoua E, Ngantchou I, Nyasse B, Denier C, Hannaert V, Shaker KH, Schneider B. Xylopioxyde and other bioactive kaurane-diterpenes from Xylopia aethiopica Dunal (Annonaceae) Journal of Applied Pharmaceutical Science. 3: 13-19. DOI: 10.7324/Japs.2013.31203 |
0.309 |
|
| 2013 |
Cano M, Rojas C, Hidalgo W, Sáez J, Gil J, Schneider B, Otálvaro F. 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 |
0.321 |
|
| 2012 |
Iranshahi M, Amanolahi F, Schneider B. New sesquiterpene coumarin from the roots of Ferula latisecta. Avicenna Journal of Phytomedicine. 2: 133-8. PMID 25050242 DOI: 10.22038/Ajp.2012.99 |
0.342 |
|
| 2012 |
Li SH, Nagy NE, Hammerbacher A, Krokene P, Niu XM, Gershenzon J, Schneider B. Localization of phenolics in phloem parenchyma cells of Norway spruce (Picea abies). Chembiochem : a European Journal of Chemical Biology. 13: 2707-13. PMID 23150460 DOI: 10.1002/Cbic.201200547 |
0.303 |
|
| 2012 |
Fang J, Reichelt M, Hidalgo W, Agnolet S, Schneider B. Tissue-specific distribution of secondary metabolites in rapeseed (Brassica napus L.). Plos One. 7: e48006. PMID 23133539 DOI: 10.1371/Journal.Pone.0048006 |
0.307 |
|
| 2012 |
Fang J, Reichelt M, Kai M, Schneider B. Metabolic profiling of lignans and other secondary metabolites from rapeseed ( Brassica napus L.). Journal of Agricultural and Food Chemistry. 60: 10523-9. PMID 23030806 DOI: 10.1021/Jf303907B |
0.376 |
|
| 2012 |
Fang J, Hölscher D, Schneider B. Co-occurrence of phenylphenalenones and flavonoids in Xiphidium caeruleum Aubl. flowers. Phytochemistry. 82: 143-8. PMID 22867904 DOI: 10.1016/J.Phytochem.2012.07.005 |
0.343 |
|
| 2012 |
Fang J, Kai M, Schneider B. Phytochemical profile of aerial parts and roots of Wachendorfia thyrsiflora L. studied by LC-DAD-SPE-NMR. Phytochemistry. 81: 144-52. PMID 22717508 DOI: 10.1016/J.Phytochem.2012.05.023 |
0.423 |
|
| 2012 |
Jirschitzka J, Schmidt GW, Reichelt M, Schneider B, Gershenzon J, D'Auria JC. 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: 10304-9. PMID 22665766 DOI: 10.1073/Pnas.1200473109 |
0.318 |
|
| 2012 |
Yan YM, Dai HQ, Du Y, Schneider B, Guo H, Li DP, Zhang LX, Fu H, Dong XP, Cheng YX. Identification of blapsins A and B as potent small-molecule 14-3-3 inhibitors from the insect Blaps japanensis. Bioorganic & Medicinal Chemistry Letters. 22: 4179-81. PMID 22578460 DOI: 10.1016/J.Bmcl.2012.04.027 |
0.321 |
|
| 2011 |
Weinhold A, Shaker K, Wenzler M, Schneider B, Baldwin IT. 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. PMID 21904938 DOI: 10.1007/S10886-011-0012-7 |
0.358 |
|
| 2011 |
Rempt M, Schneider B, Pohnert G. A reactive conjugated allene involved in the biosynthesis of volatile oxylipins in the moss dicranum scoparium Organic Letters. 13: 3229-3231. PMID 21604791 DOI: 10.1021/Ol201114G |
0.33 |
|
| 2011 |
Munde T, Maddula RK, Svatos A, Schneider B. The biosynthetic origin of oxygen functions in phenylphenalenones of Anigozanthos preissii inferred from NMR- and HRMS-based isotopologue analysis. Phytochemistry. 72: 49-58. PMID 21047660 DOI: 10.1016/J.Phytochem.2010.10.007 |
0.325 |
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| 2011 |
Ziaei A, Ramezani M, Wright L, Paetz C, Schneider B, Amirghofran Z. Identification of spathulenol in Salvia mirzayanii and the immunomodulatory effects. Phytotherapy Research : Ptr. 25: 557-62. PMID 20857430 DOI: 10.1002/Ptr.3289 |
0.305 |
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| 2011 |
Fang J, Paetz C, Hölscher D, Munde T, Schneider B. Phenylphenalenones and related natural products from Wachendorfia thyrsiflora L. Phytochemistry Letters. 4: 203-208. DOI: 10.1016/J.Phytol.2011.03.006 |
0.359 |
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| 2010 |
Shaker KH, Zinecker H, Ghani MA, Imhoff JF, Schneider B. Bioactive metabolites from the sponge Suberea sp. Chemistry & Biodiversity. 7: 2880-7. PMID 21162000 DOI: 10.1002/Cbdv.200900277 |
0.358 |
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| 2010 |
Dagvadorj E, Shaker KH, Windsor D, Schneider B, Boland W. Phenolic glucosides from Hasseltia floribunda. Phytochemistry. 71: 1900-7. PMID 20822782 DOI: 10.1016/J.Phytochem.2010.08.004 |
0.364 |
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| 2010 |
Iranshahi M, Kalategi F, Sahebkar A, Sardashti A, Schneider B. New sesquiterpene coumarins from the roots of Ferula flabelliloba. Pharmaceutical Biology. 48: 217-20. PMID 20645844 DOI: 10.3109/13880200903019226 |
0.321 |
|
| 2010 |
Bartsch M, Bednarek P, Vivancos PD, Schneider B, Von Roepenack-Lahaye E, Foyer CH, Kombrink E, Scheel D, Parker JE. Accumulation of isochorismate-derived 2,3-dihydroxybenzoic 3-O-β-D-xyloside in Arabidopsis resistance to pathogens and ageing of leaves Journal of Biological Chemistry. 285: 25654-25665. PMID 20538606 DOI: 10.1074/Jbc.M109.092569 |
0.364 |
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| 2010 |
Heiling S, Schuman MC, Schoettner M, Mukerjee P, Berger B, Schneider B, Jassbi AR, Baldwin IT. 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 Plant Cell. 22: 273-292. PMID 20081114 DOI: 10.1105/Tpc.109.071449 |
0.35 |
|
| 2010 |
Drach SV, Khripach VA, Litvinovskaya RP, Lyakhov AS, Schneider B, Zhylitskaya HA. Stereoselective synthesis of 9alpha-hydroxylated ecdysteroids. Steroids. 75: 184-8. PMID 19913044 DOI: 10.1016/J.Steroids.2009.10.011 |
0.498 |
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| 2010 |
Iranshahi M, Noroozi S, Behravan J, Karimi G, Schneider B. Persicasulphide C, a new sulphur-containing derivative from Ferula persica. Natural Product Research. 23: 1584-8. PMID 19851923 DOI: 10.1080/14786410802393571 |
0.345 |
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| 2010 |
Khripach VA, Zhabinskii VN, Zhiburtovich YY, Ivanova GV, Konstantinova OV, Tsavlovskii DV, Lorenz S, Schneider B. Preparation and synthetic application of partially protected brassinosteroids. Steroids. 75: 27-33. PMID 19786042 DOI: 10.1016/J.Steroids.2009.09.010 |
0.522 |
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| 2010 |
Hidalgo W, Duque L, Saez J, Arango R, Gil J, Rojano B, Schneider B, Otálvaro F. Structure-activity relationship in the interaction of substituted perinaphthenones with Mycosphaerella fijiensis. Journal of Agricultural and Food Chemistry. 57: 7417-21. PMID 19630386 DOI: 10.1021/Jf901052E |
0.372 |
|
| 2010 |
Fang J, Paetz C, Schneider B. Phytochemical study of the seed shell of the Myrica gale by HPLC-SPE-NMR Planta Medica. 76: 202. DOI: 10.1055/S-0030-1264500 |
0.31 |
|
| 2010 |
Duque L, Restrepo C, Sáez J, Gil J, Schneider B, Otálvaro F. Synthesis of musafluorone: a naphthoxanthenone isolated from Musa acuminata Tetrahedron Letters. 51: 4640-4643. DOI: 10.1016/J.Tetlet.2010.06.128 |
0.318 |
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| 2010 |
Jitsaeng K, Schneider B. Metabolic profiling of Musa acuminata challenged with Sporobolomyces salmonicolor Phytochemistry Letters. 3: 84-87. DOI: 10.1016/J.Phytol.2010.02.001 |
0.383 |
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| 2010 |
Cervellati C, Paetz C, Dondini L, Masia A, Schneider B. Quantitative NMR and Secondary Metabolites: a New Frontier of Phenotyping Journal of Biotechnology. 150: 475-476. DOI: 10.1016/J.Jbiotec.2010.09.717 |
0.314 |
|
| 2010 |
Schneider B. Nuclear Magnetic Resonance Spectroscopic Analysis of Enzyme Products Progress in Botany. 72: 183-208. DOI: 10.1007/978-3-642-13145-5_7 |
0.322 |
|
| 2009 |
Otálvaro F, Jitsaeng K, Munde T, Echeverri F, Quiñones W, Schneider B. O-Methylation of phenylphenalenone phytoalexins in Musaacuminata and Wachendorfia thyrsiflora. Phytochemistry. 71: 206-13. PMID 19939423 DOI: 10.1016/J.Phytochem.2009.10.019 |
0.333 |
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| 2009 |
Hölscher D, Shroff R, Knop K, Gottschaldt M, Crecelius A, Schneider B, Heckel DG, Schubert US, Svatos A. 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 : For Cell and Molecular Biology. 60: 907-18. PMID 19732382 DOI: 10.1111/J.1365-313X.2009.04012.X |
0.315 |
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| 2009 |
Moco S, Schneider B, Vervoort J. Plant micrometabolomics: the analysis of endogenous metabolites present in a plant cell or tissue. Journal of Proteome Research. 8: 1694-703. PMID 19714872 DOI: 10.1021/Pr800973R |
0.347 |
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| 2009 |
Larbat R, Hehn A, Hans J, Schneider S, Jugdé H, Schneider B, Matern U, Bourgaud F. Isolation and functional characterization of CYP71AJ4 encoding for the first P450 monooxygenase of angular furanocoumarin biosynthesis. The Journal of Biological Chemistry. 284: 4776-85. PMID 19098286 DOI: 10.1074/Jbc.M807351200 |
0.323 |
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| 2009 |
Bednarek P, Piślewska-Bednarek M, Svatoš A, Schneider B, Doubský J, Mansurova M, Humphry M, Consonni C, Panstruga R, Sanchez-Vallet A, Molina A, Schulze-Lefert P. A glucosinolate metabolism pathway in living plant cells mediates broad-spectrum antifungal defense. Science. 323: 101-106. PMID 19095900 DOI: 10.1126/Science.1163732 |
0.335 |
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| 2008 |
Vergara F, Wenzler M, Hansen BG, Kliebenstein DJ, Halkier BA, Gershenzon J, Schneider B. Determination of the absolute configuration of the glucosinolate methyl sulfoxide group reveals a stereospecific biosynthesis of the side chain. Phytochemistry. 69: 2737-42. PMID 18945459 DOI: 10.1016/J.Phytochem.2008.09.008 |
0.372 |
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| 2008 |
Köllner TG, Schnee C, Li S, Svatos A, Schneider B, Gershenzon J, Degenhardt J. 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: 20779-88. PMID 18524777 DOI: 10.1074/Jbc.M802682200 |
0.3 |
|
| 2008 |
Hölscher D, Brand S, Wenzler M, Schneider B. NMR-based metabolic profiling of Anigozanthos floral nectar. Journal of Natural Products. 71: 251-7. PMID 18197602 DOI: 10.1021/Np0705514 |
0.345 |
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| 2008 |
Tao QF, Xu Y, Lam RY, Schneider B, Dou H, Leung PS, Shi SY, Zhou CX, Yang LX, Zhang RP, Xiao YC, Wu X, Stöckigt J, Zeng S, Cheng CH, et al. Diarylheptanoids and a monoterpenoid from the rhizomes of Zingiber officinale: antioxidant and cytoprotective properties. Journal of Natural Products. 71: 12-7. PMID 18177011 DOI: 10.1021/Np070114P |
0.35 |
|
| 2008 |
Li SH, Niu XM, Zahn S, Gershenzon J, Weston J, Schneider B. Diastereomeric stilbene glucoside dimers from the bark of Norway spruce (Picea abies). Phytochemistry. 69: 772-82. PMID 18028966 DOI: 10.1016/J.Phytochem.2007.08.033 |
0.309 |
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| 2008 |
Baranovsky AV, Bolibrukh DA, Khripach VA, Schneider B. A new approach to heterocycle-modified steroids via nitrile oxide intermediates Arkivoc. 9: 29-41. DOI: 10.3998/Ark.5550190.0009.904 |
0.543 |
|
| 2008 |
Khripach VA, Zhabinskii VN, Fando GP, Khripach NB, Schneider B. Synthesis and radical oxidation of steroidal 1-oxo-5-alpha-alcohols Arkivoc. 9: 20-28. DOI: 10.3998/Ark.5550190.0009.903 |
0.499 |
|
| 2008 |
Murgu M, Santos LFA, Souza GDd, Daolio C, Schneider B, Ferreira AG, Rodrigues-Filho E. Hydroxylation of a hederagenin derived saponin by a Xylareaceous fungus found in fruits of Sapindus saponaria Journal of the Brazilian Chemical Society. 19: 831-835. DOI: 10.1590/S0103-50532008000500004 |
0.348 |
|
| 2008 |
Khripach V, Zhabinskii V, Antonchick A, Litvinovskaya R, Drach S, Sviridov O, Pryadko A, Novik T, Matveentsev V, Schneider B. A New Type of Modified Brassinosteroids for Enzyme-linked Immunosorbent Assay Natural Product Communications. 3: 1934578X0800300. DOI: 10.1177/1934578X0800300513 |
0.499 |
|
| 2008 |
Nanclares J, Gil J, Rojano B, Saez J, Schneider B, Otálvaro F. Synthesis of 4-methoxy-1H-phenalen-1-one: a subunit related to natural phenalenone-type compounds Tetrahedron Letters. 49: 3844-3847. DOI: 10.1016/J.Tetlet.2008.04.095 |
0.341 |
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| 2007 |
Iranshahi M, Mojarab M, Sadeghian H, Hanafi-Bojd MY, Schneider B. Polar secondary metabolites of Ferula persica roots. Phytochemistry. 69: 473-8. PMID 17854851 DOI: 10.1016/J.Phytochem.2007.08.001 |
0.326 |
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| 2007 |
Otálvaro F, Nanclares J, Vásquez LE, Quiñones W, Echeverri F, Arango R, Schneider B. Phenalenone-type compounds from Musa acuminata var. "Yangambi km 5" (AAA) and their activity against Mycosphaerella fijiensis. Journal of Natural Products. 70: 887-90. PMID 17428093 DOI: 10.1021/Np070091E |
0.352 |
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| 2007 |
Berim A, Schneider B, Petersen M. 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: 279-91. PMID 17333502 DOI: 10.1007/S11103-007-9151-1 |
0.334 |
|
| 2007 |
Oberthür C, Schneider B, Graf H, Hamburger M. 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 & Biodiversity. 1: 174-82. PMID 17191785 DOI: 10.1002/Cbdv.200490009 |
0.373 |
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| 2007 |
Vdovitchenko MY, Kuzovkina IN, Paetz C, Schneider B. Formation of phenolic compounds in the roots of Hedysarum theinum cultured in vitro Russian Journal of Plant Physiology. 54: 536-544. DOI: 10.1134/S1021443707040164 |
0.356 |
|
| 2007 |
Emami SA, Amin-Ar-Ramimeh E, Ahi A, Kashy MRB, Schneider B, Iranshahi M. Prenylated Flavonoids and Flavonostilbenes from Sophora pachycarpa. Roots Pharmaceutical Biology. 45: 453-457. DOI: 10.1080/13880200701389078 |
0.339 |
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| 2007 |
Khripach VA, Khripach NB, Zhabinskii VN, Zhiburtovich YY, Schneider B, de Groot A. Synthesis of [7,7-2H2]epibrassinolide Journal of Labelled Compounds and Radiopharmaceuticals. 50: 1153-1158. DOI: 10.1002/Jlcr.1408 |
0.515 |
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| 2006 |
Hölscher D, Reichert M, Görls H, Ohlenschläger O, Bringmann G, Schneider B. Monolaterol, the first configurationally assigned phenylphenalenone derivative with a stereogenic center at C-9, from Monochoria elata. Journal of Natural Products. 69: 1614-7. PMID 17125232 DOI: 10.1021/Np060192X |
0.303 |
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| 2006 |
Vergara F, Svatos A, Schneider B, Reichelt M, Gershenzon J, Wittstock U. Glycine conjugates in a lepidopteran insect herbivore--the metabolism of benzylglucosinolate in the cabbage white butterfly, Pieris rapae. Chembiochem : a European Journal of Chemical Biology. 7: 1982-9. PMID 17086559 DOI: 10.1002/Cbic.200600280 |
0.36 |
|
| 2006 |
Li SH, Schneider B, Gershenzon J. Microchemical analysis of laser-microdissected stone cells of Norway spruce by cryogenic nuclear magnetic resonance spectroscopy. Planta. 225: 771-9. PMID 17039374 DOI: 10.1007/S00425-006-0376-Z |
0.361 |
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| 2006 |
Hölscher D, Schneider B. Laser microdissection and cryogenic nuclear magnetic resonance spectroscopy: an alliance for cell type-specific metabolite profiling. Planta. 225: 763-70. PMID 17006668 DOI: 10.1007/S00425-006-0404-Z |
0.367 |
|
| 2006 |
Nyasse B, Ngantchou I, Nono JJ, Schneider B. Antifilarial activity in vitro of polycarpol and 3-O-acetyl aleuritolic acid from cameroonian medicinal plants against Onchocerca gutturosa. Natural Product Research. 20: 391-7. PMID 16644535 DOI: 10.1080/14786410600661377 |
0.322 |
|
| 2006 |
Cheng Y, Schneider B, Riese U, Schubert B, Li Z, Hamburger M. (+)-N-Deoxymilitarinone A, a neuritogenic pyridone alkaloid from the insect pathogenic fungus Paecilomyces farinosus. Journal of Natural Products. 69: 436-8. PMID 16562854 DOI: 10.1021/Np050418G |
0.313 |
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| 2006 |
Brand S, Hölscher D, Schierhorn A, Svatos A, Schröder J, Schneider B. A type III polyketide synthase from Wachendorfia thyrsiflora and its role in diarylheptanoid and phenylphenalenone biosynthesis. Planta. 224: 413-28. PMID 16496097 DOI: 10.1007/S00425-006-0228-X |
0.326 |
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| 2006 |
Antonchick AP, Svatoš A, Konstantinova OV, Zhabinskii VN, Khripach VA, Schneider B. Reversible Conversion In The Brassinosteroid Quartet Castasterone, Brassinolide And Their 3β-Epimers Zeitschrift FüR Naturforschung B. 61: 1039-1044. DOI: 10.1515/Znb-2006-0817 |
0.537 |
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| 2006 |
Kuzovkina IN, Schneider B. 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 |
0.309 |
|
| 2005 |
Schliemann W, Schneider B, Wray V, Schmidt J, Nimtz M, Porzel A, Böhm H. Flavonols and an indole alkaloid skeleton bearing identical acylated glycosidic groups from yellow petals of Papaver nudicaule. Phytochemistry. 67: 191-201. PMID 16376394 DOI: 10.1016/J.Phytochem.2005.11.002 |
0.336 |
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| 2005 |
Vogelsang K, Schneider B, Petersen M. 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: 369-73. PMID 16133208 DOI: 10.1007/S00425-005-0089-8 |
0.302 |
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| 2005 |
Schneider B, Paetz C, Hölscher D, Opitz S. HPLC-NMR for tissue-specific analysis of phenylphenalenone-related compounds in Xiphidium caeruleum (Haemodoraceae). Magnetic Resonance in Chemistry : Mrc. 43: 724-8. PMID 16049956 DOI: 10.1002/Mrc.1634 |
0.379 |
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| 2005 |
Bednarek P, Schneider B, Svatos A, Oldham NJ, Hahlbrock K. Structural complexity, differential response to infection, and tissue specificity of indolic and phenylpropanoid secondary metabolism in Arabidopsis roots. Plant Physiology. 138: 1058-70. PMID 15923335 DOI: 10.1104/Pp.104.057794 |
0.368 |
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| 2005 |
Khripach VA, Zhabinskii VN, Konstantinova OV, Khripach NB, Antonchick AV, Antonchick AP, Schneider B. Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids. Steroids. 70: 551-62. PMID 15894040 DOI: 10.1016/J.Steroids.2005.02.014 |
0.676 |
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| 2005 |
Antonchick A, Svatos A, Schneider B, Konstantinova OV, Zhabinskii VN, Khripach VA. 2,3-Epoxybrassinosteroids are intermediates in the biosynthesis of castasterone in seedlings of Secale cereale. Phytochemistry. 66: 65-72. PMID 15649512 DOI: 10.1016/J.Phytochem.2004.11.008 |
0.651 |
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| 2005 |
Hölscher D, Schneider B. The biosynthesis of 8-phenylphenalenones from Eichhornia crassipes involves a putative aryl migration step. Phytochemistry. 66: 59-64. PMID 15649511 DOI: 10.1016/J.Phytochem.2004.10.019 |
0.372 |
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| 2005 |
Cheng Y, Schneider B, Riese U, Schubert B, Li Z, Hamburger M. Farinosones A-C, neurotrophic alkaloidal metabolites from the entomogenous deuteromycete Paecilomyces farinosus. Journal of Natural Products. 67: 1854-8. PMID 15568775 DOI: 10.1021/Np049761W |
0.365 |
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| 2004 |
Antonchick AP, Schneider B, Zhabinskii VN, Khripach VA. Synthesis of [26,27-2H6]brassinosteroids from 23,24-bisnorcholenic acid methyl ester. Steroids. 69: 617-28. PMID 15465106 DOI: 10.1016/J.Steroids.2004.05.014 |
0.682 |
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| 2004 |
Kuzovkina I, Al'terman I, Schneider B. Specific accumulation and revised structures of acridone alkaloid glucosides in the tips of transformed roots of Ruta graveolens. Phytochemistry. 65: 1095-100. PMID 15110689 DOI: 10.1016/J.Phytochem.2004.03.003 |
0.382 |
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| 2004 |
Schüler G, Mithöfer A, Baldwin IT, Berger S, Ebel J, Santos JG, Herrmann G, Hölscher D, Kramell R, Kutchan TM, Maucher H, Schneider B, Stenzel I, Wasternack C, Boland W. Coronalon: A powerful tool in plant stress physiology Febs Letters. 563: 17-22. PMID 15063716 DOI: 10.1016/S0014-5793(04)00239-X |
0.34 |
|
| 2004 |
Svatos A, Antonchick A, Schneider B. Determination of brassinosteroids in the sub-femtomolar range using dansyl-3-aminophenylboronate derivatization and electrospray mass spectrometry. Rapid Communications in Mass Spectrometry : Rcm. 18: 816-21. PMID 15052565 DOI: 10.1002/Rcm.1413 |
0.591 |
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| 2004 |
Tan J, Bednarek P, Liu J, Schneider B, Svatos A, Hahlbrock K. Universally occurring phenylpropanoid and species-specific indolic metabolites in infected and uninfected Arabidopsis thaliana roots and leaves. Phytochemistry. 65: 691-9. PMID 15016565 DOI: 10.1016/J.Phytochem.2003.12.009 |
0.391 |
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| 2004 |
Nookandeh A, Frank N, Steiner F, Ellinger R, Schneider B, Gerhäuser C, Becker H. Xanthohumol metabolites in faeces of rats. Phytochemistry. 65: 561-70. PMID 15003419 DOI: 10.1016/J.Phytochem.2003.11.016 |
0.342 |
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| 2003 |
Antonchick AP, Schneider B, Zhabinskii VN, Konstantinova OV, Khripach VA. Biosynthesis of 2,3-epoxybrassinosteroids in seedlings of Secale cereale. Phytochemistry. 63: 771-6. PMID 12877917 DOI: 10.1016/S0031-9422(03)00354-6 |
0.641 |
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| 2003 |
Opitz S, Schneider B. Oxidative biosynthesis of phenylbenzoisochromenones from phenylphenalenones. Phytochemistry. 62: 307-12. PMID 12620342 DOI: 10.1016/S0031-9422(02)00546-0 |
0.307 |
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| 2003 |
Eckermann C, Schröder G, Eckermann S, Strack D, Schmidt J, Schneider B, Schröder J. Stilbenecarboxylate biosynthesis: a new function in the family of chalcone synthase-related proteins. Phytochemistry. 62: 271-86. PMID 12620338 DOI: 10.1016/S0031-9422(02)00554-X |
0.307 |
|
| 2003 |
Opitz S, Schneider B. Organ-specific analysis of phenylphenalenone-related compounds in Xiphidium caeruleum. Phytochemistry. 61: 819-25. PMID 12453574 DOI: 10.1016/S0031-9422(02)00359-X |
0.355 |
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| 2003 |
Baranovsky A, Schmitt B, Fowler DJ, Schneider B. Synthesis of new biosynthetically important diarylheptanoids and their oxa- and fluoro-analogues by three different strategies Synthetic Communications. 33: 1019-1045. DOI: 10.1081/Scc-120016367 |
0.358 |
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| 2003 |
Schneider B, Gershenzon J, Graser G, Hölscher D, Schmitt B. 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 |
0.366 |
|
| 2002 |
Opitz S, Schnitzler JP, Hause B, Schneider B. Histochemical analysis of phenylphenalenone-related compounds in Xiphidium caeruleum (Haemodoraceae). Planta. 216: 881-9. PMID 12624776 DOI: 10.1007/S00425-002-0941-Z |
0.366 |
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| 2002 |
Khripach VA, Zhabinskii VN, Antonchick AP, Konstantinova OV, Schneider B. Synthesis of hexadeuterated 23-dehydroxybrassinosteroids. Steroids. 67: 1101-8. PMID 12441196 DOI: 10.1016/S0039-128X(02)00071-5 |
0.692 |
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| 2002 |
Opitz S, Hölscher D, Oldham NJ, Bartram S, Schneider B. Phenylphenalenone-related compounds: chemotaxonomic markers of the haemodoraceae from Xiphidium caeruleum. Journal of Natural Products. 65: 1122-30. PMID 12193015 DOI: 10.1021/Np020083S |
0.361 |
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| 2002 |
Khripach VA, Zhabinskii VN, Konstantinova OV, Khripach NB, Antonchick AP, Schneider B. [3,3]-Claisen rearrangements in 24alpha-methyl steroid synthesis. Application to campesterol, crinosterol, and Delta25-crinosterol side chain construction. Steroids. 67: 597-603. PMID 11996932 DOI: 10.1016/S0039-128X(02)00007-7 |
0.667 |
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| 2002 |
Khripach VA, Zhabinskii VN, Konstantinova OV, Antonchick AP, Schneider B. Synthesis of [26-2H(3)]brassinosteroids. Steroids. 67: 587-95. PMID 11996931 DOI: 10.1016/S0039-128X(02)00004-1 |
0.677 |
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| 2002 |
Berlich M, Menge S, Bruns I, Schmidt J, Schneider B, Krauss GJ. Coumarins give misleading absorbance with Ellman's reagent suggestive of thiol conjugates. The Analyst. 127: 333-6. PMID 11996355 DOI: 10.1039/B110988J |
0.379 |
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| 2002 |
Otálvaro F, Görls H, Hölscher D, Schmitt B, Echeverri F, Quiñones W, Schneider B. Dimeric phenylphenalenones from Musa acuminata and various Haemodoraceae species. Crystal structure of anigorootin. Phytochemistry. 60: 61-6. PMID 11985853 DOI: 10.1016/S0031-9422(02)00066-3 |
0.342 |
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| 2002 |
Reichelt M, Brown PD, Schneider B, Oldham NJ, Stauber E, Tokuhisa J, Kliebenstein DJ, Mitchell-Olds T, Gershenzon J. Benzoic acid glucosinolate esters and other glucosinolates from Arabidopsis thaliana. Phytochemistry. 59: 663-71. PMID 11867099 DOI: 10.1016/S0031-9422(02)00014-6 |
0.429 |
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| 2002 |
Stündl U, Schneider B. 3Beta-brassinosteroid dehydrogenase activity in Arabidopsis and tomato. Phytochemistry. 58: 989-94. PMID 11730861 DOI: 10.1016/S0031-9422(01)00387-9 |
0.322 |
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| 2002 |
Schmitt B, Schneider B. Phenylpropanoid interconversion in Anigozanthos preissii observed by high-performance liquid chromatography-nuclear magnetic resonance spectroscopy. Phytochemical Analysis : Pca. 12: 43-7. PMID 11704960 DOI: 10.1002/1099-1565(200101/02)12:1<43::Aid-Pca546>3.0.Co;2-Z |
0.329 |
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| 2002 |
Otálvaro F, Echeverri F, Quiñones W, Torres F, Schneider B. Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene Triol Molecules. 7: 331-340. DOI: 10.3390/70300331 |
0.313 |
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| 2001 |
Sicker D, Schneider B, Hennig L, Knop M, Schulz M. Glycoside carbamates from benzoxazolin-2(3H)-one detoxification in extracts and exudates of corn roots Phytochemistry. 58: 819-825. PMID 11672748 DOI: 10.1016/S0031-9422(01)00299-0 |
0.329 |
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| 2001 |
Hagemeier J, Schneider B, Oldham NJ, Hahlbrock K. 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: 753-8. PMID 11136235 DOI: 10.1073/Pnas.98.2.753 |
0.365 |
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| 2001 |
Konstantinova OV, Antonchick AP, Oldham NJ, Zhabinskii VN, Khripach VA, Schneider B. Analysis of underivatized brassinosteroids by HPLC/APCI-MS. Occurrence of 3-epibrassinolide in Arabidopsis thaliana Collection of Czechoslovak Chemical Communications. 66: 1729-1734. DOI: 10.1135/Cccc20011729 |
0.684 |
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| 2001 |
Gräther O, Schneider B. The Metabolic Diversity of Plant Cell and Tissue Cultures Progress in Botany. 62: 266-304. DOI: 10.1007/978-3-642-56849-7_13 |
0.355 |
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| 2001 |
Andres H, Sidorov G, Zverkov Y, Myasoedov N, Cimpoia A, Susan A, Saljoughian M, Morimoto H, Williams PG, Than C, Salter R, Moenius T, Ackermann P, Studer M, Morgan A, ... ... Schneider B, et al. 9thConference of the Central European Division e.V. of the International Isotope Society Journal of Labelled Compounds and Radiopharmaceuticals. 44: 947-985. DOI: 10.1002/Jlcr.527 |
0.624 |
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| 2000 |
Hölscher D, Schneider B. Phenalenones from Strelitzia reginae. Journal of Natural Products. 63: 1027-8. PMID 10924194 DOI: 10.1021/Np000035C |
0.332 |
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| 2000 |
Graser G, Schneider B, Oldham NJ, Gershenzon J. The methionine chain elongation pathway in the biosynthesis of glucosinolates in Eruca sativa (Brassicaceae). Archives of Biochemistry and Biophysics. 378: 411-9. PMID 10860559 DOI: 10.1006/Abbi.2000.1812 |
0.349 |
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| 2000 |
Schmitt B, Hölscher D, Schneider B. Variability of phenylpropanoid precursors in the biosynthesis of phenylphenalenones in Anigozanthos preissii. Phytochemistry. 53: 331-7. PMID 10703053 DOI: 10.1016/S0031-9422(99)00544-0 |
0.306 |
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| 1999 |
Schupp P, Eder C, Proksch P, Wray V, Schneider B, Herderich M, Paul V. Staurosporine derivatives from the ascidian eudistoma toealensis and its predatory flatworm pseudoceros sp Journal of Natural Products. 62: 959-962. PMID 10425116 DOI: 10.1021/Np980527D |
0.321 |
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| 1999 |
Schmitt B, Schneider B. Dihydrocinnamic acids are involved in the biosynthesis of phenylphenalenones in Anigozanthos preissii Phytochemistry. 52: 45-53. DOI: 10.1016/S0031-9422(99)00116-8 |
0.357 |
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| 1999 |
Hölscher D, Schneider B. HPLC-NMR analysis of phenylphenalenones and a stilbene from Anigozanthos flavidus1Dedicated to Professor Günter Adam on the occasion of his sixty-fifth birthday.1 Phytochemistry. 50: 155-161. DOI: 10.1016/S0031-9422(98)00495-6 |
0.359 |
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| 1999 |
Zhao Y, Nookandeh A, Schneider B, Sun X, Schmitt B, Stöckigt J. Lignans from Torreya jackii identified by stopped-flow high-performance liquid chromatography–nuclear magnetic resonance spectroscopy Journal of Chromatography A. 837: 83-91. DOI: 10.1016/S0021-9673(99)00050-3 |
0.33 |
|
| 1998 |
Maier W, Schneider B, Strack D. Biosynthesis of sesquiterpenoid cyclohexenone derivatives in mycorrhizal barley roots proceeds via the glyceraldehyde 3-phosphate/pyruvate pathway Tetrahedron Letters. 39: 521-524. DOI: 10.1016/S0040-4039(97)10673-6 |
0.324 |
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| 1998 |
Hölscher D, Schneider B. Phenylphenalenones from Ensete ventricosum Phytochemistry. 49: 2155-2157. DOI: 10.1016/S0031-9422(98)00423-3 |
0.317 |
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| 1998 |
Kolbe A, Schneider B, Porzel A, Adam G. Metabolic inversion of the 3-hydroxy function of brassinosteroids Phytochemistry. 48: 467-470. DOI: 10.1016/S0031-9422(98)00037-5 |
0.342 |
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| 1998 |
Wieland I, Kluge M, Schneider B, Schmidt J, Sicker D, Schulz M. 3-β-d-glucopyranosyl-benzoxazolin-2(3H)-one—A detoxification product of benzoxazolin-2(3H)-one in oat roots Phytochemistry. 49: 719-722. DOI: 10.1016/S0031-9422(97)91012-8 |
0.345 |
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| 1998 |
Kolbe A, Schneider B, Voigt B, Adam G. Labelling of biogenetic brassinosteroid precursors Journal of Labelled Compounds and Radiopharmaceuticals. 41: 131-137. DOI: 10.1002/(Sici)1099-1344(199802)41:2<131::Aid-Jlcr59>3.0.Co;2-F |
0.335 |
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| 1997 |
Hölscher D, Schneider B. Phenylphenalenones from root cultures of Anigozanthos preissii Phytochemistry. 45: 87-91. DOI: 10.1016/S0031-9422(96)00679-6 |
0.381 |
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| 1997 |
Schneider B. In-vivo nuclear magnetic resonance spectroscopy of low-molecular-weight compounds in plant cells Planta. 203: 1-8. DOI: 10.1007/S00050158 |
0.361 |
|
| 1996 |
Hai T, Schneider B, Porzel A, Adam G. Metabolism of 24-epi-castasterone in cell suspension cultures of Lycopersicon esculentum Phytochemistry. 41: 197-201. DOI: 10.1016/0031-9422(95)00585-4 |
0.322 |
|
| 1996 |
Kolbe A, Schneider B, Porzel A, Adam G. Metabolism of 24-epi-castasterone and 24-epi-brassinolide in cell suspension cultures of Ornithopus sativus Phytochemistry. 41: 163-167. DOI: 10.1016/0031-9422(95)00546-3 |
0.328 |
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| 1995 |
Hölscher D, Schneider B. A diarylheptanoid intermediate in the biosynthesis of phenylphenalenones in Anigozanthos preissii Journal of the Chemical Society, Chemical Communications. 525-526. DOI: 10.1039/C39950000525 |
0.309 |
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| 1995 |
Hai T, Schneider B, Adam G. Metabolic conversion of 24-epi-brassinolide into pentahydroxylated brassinosteroid glucosides in tomato cell cultures Phytochemistry. 40: 443-448. DOI: 10.1016/0031-9422(95)00224-U |
0.318 |
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| 1995 |
Kolbe A, Schneider B, Porzel A, Schmidt J, Adam G. Acyl-conjugated metabolites of brassinosteroids in cell suspension cultures of Ornithopus sativus Phytochemistry. 38: 633-636. DOI: 10.1016/0031-9422(94)00742-C |
0.332 |
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| 1994 |
Schneider B, Stock M, Bohm H, Schneider G, Schütte H, Schreiber K, Brauner A, Köster J, Kaußmann EU. Metabolism of amitrole in apple: III. Model systems Pesticide Science. 41: 327-333. DOI: 10.1002/Ps.2780410407 |
0.323 |
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| 1993 |
Schneider B, Ahrens U, Kirkpatrick BC, Seemuller E. Classification of plant-apthogenic mycoplasma-like organism using restriction-site analysis of PCR-amplified 16S rDNA Journal of General Microbiology. 139: 519-527. DOI: 10.1099/00221287-139-3-519 |
0.313 |
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| 1993 |
Bärenwald G, Schneider B, Schütte HR. Metabolism of the bisethyleneglycolesters of 2,4-D and MCPA in barley Phytochemistry. 32: 523-526. DOI: 10.1016/S0031-9422(00)95130-6 |
0.334 |
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| 1993 |
Schneider B, Zenk MH. Metabolism of (S)-reticuline in an alkaloid non-producing cell culture strain of Thalictrum tuberosum Phytochemistry. 33: 1431-1435. DOI: 10.1016/0031-9422(93)85104-Y |
0.339 |
|
| 1993 |
Schneider B, Stock M, Schütte HR, Schreiber K, Köster J, Kaußmann EU. Metabolism of amitrole in apple: II. Bound residues from mature fruits Pesticide Science. 37: 9-13. DOI: 10.1002/Ps.2780370103 |
0.326 |
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| 1992 |
Schaller B, Schneider B, Schütte HR. Metabolism of the Herbicide Bromoxynil in Hordeum vulgare and Stellaria media Zeitschrift FüR Naturforschung C. 47: 126-131. DOI: 10.1515/Znc-1992-1-221 |
0.316 |
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| 1992 |
Schneider B, Stock M, Schneider G, Schütte HR, Schreiber K, Brauner A, Kaußmann EU. Metabolism of Amitrole in Apple: I. Soluble Metabolites from Mature Fruits Zeitschrift FüR Naturforschung C. 47: 120-125. DOI: 10.1515/Znc-1992-1-220 |
0.349 |
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| 1991 |
Schaller B, Schneider B, Schütte HR. Investigations on the selectivity and the metabolism of the herbicide bromoxynil in plants Journal of Plant Physiology. 139: 243-245. DOI: 10.1016/S0176-1617(11)80616-4 |
0.34 |
|
| 1989 |
Bärenwald G, Schneider B, Schutte HR. Comparative investigations on the metabolism of the herbicide 2(2,4-dichlorphenoxy)-propionic acid in plants and cultured cells of tomato Zeitschrift FüR Naturforschung. 44: 233-236. DOI: 10.1515/Znc-1989-3-410 |
0.323 |
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| 1989 |
Schneider B, Kolbe A, Stock M, Bernasch A. Synthese von radioaktiv markierten Pestiziden und deren Anwendung für Untersuchungen von Metabolismus und Verhalten in Pflanzen und im Boden Isotopes in Environmental and Health Studies. 25: 309-316. DOI: 10.1080/10256018908624141 |
0.322 |
|
| 1987 |
Bärenwald G, Schneider B, Schütte H. Metabolism of the Herbicide 2-(2,4-Dichlorophenoxy)-propionic Acid (Dichlorprop) in Barley (Hordeum vulgare) Zeitschrift FüR Naturforschung C. 42: 486-490. DOI: 10.1515/Znc-1987-0426 |
0.382 |
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| 1987 |
Schneider B, Schütte HR, Günther G, Köhler S. Metabolism of 2-(2,4-dichlorophenoxy)-isobutyric acid and its glucosyl ester in plants and suspension cultured cells of Agrostemma githago Journal of Plant Physiology. 127: 147-152. DOI: 10.1016/S0176-1617(87)80048-2 |
0.327 |
|
| 1986 |
Schneider B, Schütte H, Preiss A. Metabolism of the Plant Growth Regulator (E)-[3H]2-Ethylhex-2-enoic Acid in Hordeum vulgare Zeitschrift FüR Naturforschung C. 41: 141-147. DOI: 10.1515/Znc-1986-1-221 |
0.355 |
|
| 1984 |
Schneider B, Schütte HR, Tewes A. Comparative Investigations on the Metabolism of 2-(2,4-Dichlorophenoxy)Isobutyric Acid in Plants and Cell Suspension Cultures of Lycopersicon esculentum Plant Physiology. 76: 989-992. PMID 16663986 DOI: 10.1104/Pp.76.4.989 |
0.357 |
|
| 1980 |
AUGUSTIN M, FISCHER G, SCHNEIDER B, KOEHLER M. ChemInform Abstract: REACTIONS OF 2,3-DICHLOROMALEIMIDES WITH METHYLENE-ACTIVE COMPOUNDS Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198002209 |
0.61 |
|
| 1979 |
Augustin M, Fischer G, Schneider B, Köhler M. Reaktionen von 2,3-Dichlormaleinimiden mit methylaktiven Verbindungen Journal Fur Praktische Chemie-Chemiker-Zeitung. 321: 787-796. DOI: 10.1002/Prac.19793210510 |
0.328 |
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