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M Soledade C. Pedras - Publications

Affiliations: 
1994- Chemistry University of Saskatchewan, Saskatoon, SK, Canada 
Area:
Organic Chemistry, Plant Pathology Agriculture
Website:
http://artsandscience.usask.ca/profile/MPedras#/profile
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Year Citation  Score
2017 Pedras MS, To QH. Defense and signalling metabolites of the crucifer Erucastrum canariense: Synchronized abiotic induction of phytoalexins and galacto-oxylipins. Phytochemistry. 139: 18-24. PMID 28390240 DOI: 10.1016/J.Phytochem.2017.03.005  0.333
2017 Pedras MS, Abdoli A. Biotransformation of rutabaga phytoalexins by the fungus Alternaria brassicicola: Unveiling the first hybrid metabolite derived from a phytoalexin and a fungal polyketide. Bioorganic & Medicinal Chemistry. 25: 557-567. PMID 27884513 DOI: 10.1016/J.Bmc.2016.11.017  0.448
2016 Pedras MS, Park MR. The biosynthesis of brassicicolin A in the phytopathogen Alternaria brassicicola. Phytochemistry. PMID 27665682 DOI: 10.1016/J.Phytochem.2016.09.009  0.37
2016 Pedras MS, To QH. Unveiling the first indole-fused thiazepine: structure, synthesis and biosynthesis of cyclonasturlexin, a remarkable cruciferous phytoalexin. Chemical Communications (Cambridge, England). 52: 5880-3. PMID 27052411 DOI: 10.1039/c6cc02108e  0.366
2015 Pedras MS, Alavi M, To QH. Expanding the nasturlexin family: Nasturlexins C and D and their sulfoxides are phytoalexins of the crucifers Barbarea vulgaris and B. verna. Phytochemistry. 118: 131-8. PMID 26318326 DOI: 10.1016/J.Phytochem.2015.08.009  0.435
2015 Pedras MS, Park MR. Metabolite diversity in the plant pathogen Alternaria brassicicola: factors affecting production of brassicicolin A, depudecin, phomapyrone A and other metabolites. Mycologia. 107: 1138-50. PMID 26297782 DOI: 10.3852/15-054  0.367
2015 Pedras MS, Yaya EE. Plant chemical defenses: are all constitutive antimicrobial metabolites phytoanticipins? Natural Product Communications. 10: 209-18. PMID 25920246 DOI: 10.1177/1934578X1501000142  0.446
2015 Pedras MS, To QH. Non-indolyl cruciferous phytoalexins: Nasturlexins and tridentatols, a striking convergent evolution of defenses in terrestrial plants and marine animals? Phytochemistry. 113: 57-63. PMID 25152450 DOI: 10.1016/J.Phytochem.2014.07.024  0.506
2014 Pedras MS, Yaya EE. Tenualexin, other phytoalexins and indole glucosinolates from wild cruciferous species. Chemistry & Biodiversity. 11: 910-8. PMID 24934676 DOI: 10.1002/Cbdv.201300260  0.421
2014 Grubb CD, Zipp BJ, Kopycki J, Schubert M, Quint M, Lim EK, Bowles DJ, Pedras MS, Abel S. Comparative analysis of Arabidopsis UGT74 glucosyltransferases reveals a special role of UGT74C1 in glucosinolate biosynthesis. The Plant Journal : For Cell and Molecular Biology. 79: 92-105. PMID 24779768 DOI: 10.1111/Tpj.12541  0.4
2014 Pedras MS, Minic Z, Abdoli A. The phytoalexin camalexin induces fundamental changes in the proteome of Alternaria brassicicola different from those caused by brassinin. Fungal Biology. 118: 83-93. PMID 24433679 DOI: 10.1016/J.Funbio.2013.11.005  0.312
2013 Pedras MS, Abdoli A. Metabolism of the phytoalexins camalexins, their bioisosteres and analogues in the plant pathogenic fungus Alternaria brassicicola. Bioorganic & Medicinal Chemistry. 21: 4541-9. PMID 23773956 DOI: 10.1016/J.Bmc.2013.05.026  0.445
2013 Pedras MS, Yaya EE. Dissecting metabolic puzzles through isotope feeding: a novel amino acid in the biosynthetic pathway of the cruciferous phytoalexins rapalexin A and isocyalexin A. Organic & Biomolecular Chemistry. 11: 1149-66. PMID 23306875 DOI: 10.1039/C2Ob27076E  0.454
2013 Pedras MS, Abdoli A, Chumala PB, Saha P, Schatte G. Unprecedented spirocyclization of 3-methyleneindoline-2-thiones during hydrolysis of the phytoalexin cyclobrassinin. Bioorganic & Medicinal Chemistry Letters. 23: 484-7. PMID 23232058 DOI: 10.1016/J.Bmcl.2012.11.042  0.445
2013 Kopycki J, Wieduwild E, Kohlschmidt J, Brandt W, Stepanova AN, Alonso JM, Pedras MS, Abel S, Grubb CD. Kinetic analysis of Arabidopsis glucosyltransferase UGT74B1 illustrates a general mechanism by which enzymes can escape product inhibition. The Biochemical Journal. 450: 37-46. PMID 23150922 DOI: 10.1042/Bj20121403  0.381
2012 Pedras MS, Sarma-Mamillapalle VK. Metabolism and metabolites of dithiocarbamates in the plant pathogenic fungus Leptosphaeria maculans. Journal of Agricultural and Food Chemistry. 60: 7792-8. PMID 22823278 DOI: 10.1021/Jf302038A  0.447
2012 Pedras MS, Sarma-Mamillapalle VK. The cruciferous phytoalexins rapalexin A, brussalexin A and erucalexin: chemistry and metabolism in Leptosphaeria maculans. Bioorganic & Medicinal Chemistry. 20: 3991-6. PMID 22672981 DOI: 10.1016/J.Bmc.2012.05.020  0.457
2012 Pedras MS, Yaya EE. The first isocyanide of plant origin expands functional group diversity in cruciferous phytoalexins: synthesis, structure and bioactivity of isocyalexin A. Organic & Biomolecular Chemistry. 10: 3613-6. PMID 22495624 DOI: 10.1039/C2Ob25492A  0.449
2012 Pedras MS, Khallaf I. Molecular interactions of the phytotoxins destruxin B and sirodesmin PL with crucifers and cereals: metabolism and elicitation of plant defenses. Phytochemistry. 77: 129-39. PMID 22414311 DOI: 10.1016/J.Phytochem.2012.02.010  0.379
2012 Pedras MS, Minic Z, Hossain S. Discovery of inhibitors and substrates of brassinin hydrolase: Probing selectivity with dithiocarbamate bioisosteres. Bioorganic & Medicinal Chemistry. 20: 225-33. PMID 22137599 DOI: 10.1016/J.Bmc.2011.11.009  0.363
2011 Pedras MS, Hossain S. Interaction of cruciferous phytoanticipins with plant fungal pathogens: indole glucosinolates are not metabolized but the corresponding desulfo-derivatives and nitriles are. Phytochemistry. 72: 2308-16. PMID 21920565 DOI: 10.1016/J.Phytochem.2011.08.018  0.523
2011 Pedras MS, Yaya EE, Glawischnig E. The phytoalexins from cultivated and wild crucifers: chemistry and biology. Natural Product Reports. 28: 1381-405. PMID 21681321 DOI: 10.1039/C1Np00020A  0.501
2011 Pedras MS, Minic Z, Sarma-Mamillapalle VK. Brassinin oxidase mediated transformation of the phytoalexin brassinin: structure of the elusive co-product, deuterium isotope effect and stereoselectivity. Bioorganic & Medicinal Chemistry. 19: 1390-9. PMID 21292494 DOI: 10.1016/J.Bmc.2011.01.011  0.356
2011 Pedras MS, Hossain S, Snitynsky RB. Detoxification of cruciferous phytoalexins in Botrytis cinerea: spontaneous dimerization of a camalexin metabolite. Phytochemistry. 72: 199-206. PMID 21176925 DOI: 10.1016/J.Phytochem.2010.11.018  0.497
2010 Pedras MS, Minic Z, Thongbam PD, Bhaskar V, Montaut S. Indolyl-3-acetaldoxime dehydratase from the phytopathogenic fungus Sclerotinia sclerotiorum: purification, characterization, and substrate specificity. Phytochemistry. 71: 1952-62. PMID 21036375 DOI: 10.1016/J.Phytochem.2010.10.002  0.382
2010 Pedras MS, Yaya EE, Hossain S. Unveiling the phytoalexin biosynthetic puzzle in salt cress: unprecedented incorporation of glucobrassicin into wasalexins A and B. Organic & Biomolecular Chemistry. 8: 5150-8. PMID 20848032 DOI: 10.1039/C0Ob00265H  0.402
2010 Pedras MS, Yaya EE. Phytoalexins from Brassicaceae: news from the front. Phytochemistry. 71: 1191-7. PMID 20416910 DOI: 10.1016/J.Phytochem.2010.03.020  0.414
2010 Pedras MS, Minic Z, Sarma-Mamillapalle VK, Suchy M. Discovery of inhibitors of brassinin oxidase based on the scaffolds of the phytoalexins brassilexin and wasalexin. Bioorganic & Medicinal Chemistry. 18: 2456-63. PMID 20303277 DOI: 10.1016/J.Bmc.2010.02.054  0.344
2009 Pedras MS, Minic Z, Sarma-Mamillapalle VK. Substrate specificity and inhibition of brassinin hydrolases, detoxifying enzymes from the plant pathogens Leptosphaeria maculans and Alternaria brassicicola. The Febs Journal. 276: 7412-28. PMID 19922473 DOI: 10.1111/J.1742-4658.2009.07457.X  0.398
2009 Pedras MS, Yu Y. Phytotoxins, elicitors and other secondary metabolites from phytopathogenic "blackleg" fungi: structure, phytotoxicity and biosynthesis. Natural Product Communications. 4: 1291-304. PMID 19831047 DOI: 10.1177/1934578X0900400927  0.39
2009 Pedras MS, Okinyo-Owiti DP, Thoms K, Adio AM. The biosynthetic pathway of crucifer phytoalexins and phytoanticipins: de novo incorporation of deuterated tryptophans and quasi-natural compounds. Phytochemistry. 70: 1129-38. PMID 19560792 DOI: 10.1016/J.Phytochem.2009.05.015  0.363
2009 Pedras MS, Yu Y. Salt stress induces production of melanin related metabolites in the phytopathogenic fungus Leptosphaeria maculans. Natural Product Communications. 4: 53-8. PMID 19370875 DOI: 10.1177/1934578X0900400113  0.387
2009 Pedras MS, Minic Z, Sarma-Mamillapalle VK. Synthetic inhibitors of the fungal detoxifying enzyme brassinin oxidase based on the phytoalexin camalexin scaffold. Journal of Agricultural and Food Chemistry. 57: 2429-35. PMID 19243099 DOI: 10.1021/Jf803666S  0.455
2009 Pedras MS, Chumala PB, Jin W, Islam MS, Hauck DW. The phytopathogenic fungus Alternaria brassicicola: phytotoxin production and phytoalexin elicitation. Phytochemistry. 70: 394-402. PMID 19223049 DOI: 10.1016/J.Phytochem.2009.01.005  0.464
2008 Pedras MS, Yu Y. Structure and biological activity of maculansin A, a phytotoxin from the phytopathogenic fungus Leptosphaeria maculans. Phytochemistry. 69: 2966-71. PMID 18977007 DOI: 10.1016/J.Phytochem.2008.09.015  0.452
2008 Pedras MS, Zheng QA, Strelkov S. Metabolic changes in roots of the oilseed canola infected with the biotroph Plasmodiophora brassicae: phytoalexins and phytoanticipins. Journal of Agricultural and Food Chemistry. 56: 9949-61. PMID 18834132 DOI: 10.1021/Jf802192F  0.369
2008 Pedras MS, Yu Y. Stress-driven discovery of metabolites from the phytopathogenic fungus Leptosphaeria maculans: structure and activity of leptomaculins A-E. Bioorganic & Medicinal Chemistry. 16: 8063-71. PMID 18701303 DOI: 10.1016/J.Bmc.2008.07.060  0.442
2008 Pedras MS, Minic Z, Jha M. Brassinin oxidase, a fungal detoxifying enzyme to overcome a plant defense -- purification, characterization and inhibition. The Febs Journal. 275: 3691-705. PMID 18549452 DOI: 10.1111/j.1742-4658.2008.06513.x  0.324
2008 Pedras MS. The chemical ecology of crucifers and their fungal pathogens: boosting plant defenses and inhibiting pathogen invasion. Chemical Record (New York, N.Y.). 8: 109-15. PMID 18383155 DOI: 10.1002/Tcr.20140  0.451
2008 Pedras MS, Adio AM. Phytoalexins and phytoanticipins from the wild crucifers Thellungiella halophila and Arabidopsis thaliana: rapalexin A, wasalexins and camalexin. Phytochemistry. 69: 889-93. PMID 18078965 DOI: 10.1016/J.Phytochem.2007.10.032  0.318
2008 Pedras MS, Okinyo DP. Remarkable incorporation of the first sulfur containing indole derivative: another piece in the biosynthetic puzzle of crucifer phytoalexins. Organic & Biomolecular Chemistry. 6: 51-4. PMID 18075646 DOI: 10.1039/B714743K  0.379
2008 Pedras MS, Zheng QA, Gadagi RS, Rimmer SR. Phytoalexins and polar metabolites from the oilseeds canola and rapeseed: differential metabolic responses to the biotroph Albugo candida and to abiotic stress. Phytochemistry. 69: 894-910. PMID 18039546 DOI: 10.1016/J.Phytochem.2007.10.019  0.472
2007 Pedras MS, Jha M, Minic Z, Okeola OG. Isosteric probes provide structural requirements essential for detoxification of the phytoalexin brassinin by the fungal pathogen Leptosphaeria maculans. Bioorganic & Medicinal Chemistry. 15: 6054-61. PMID 17616463 DOI: 10.1016/J.Bmc.2007.06.040  0.399
2007 Pedras MS, Hossain M. Design, synthesis, and evaluation of potential inhibitors of brassinin glucosyltransferase, a phytoalexin detoxifying enzyme from Sclerotinia sclerotiorum. Bioorganic & Medicinal Chemistry. 15: 5981-96. PMID 17590338 DOI: 10.1016/J.Bmc.2007.05.072  0.443
2007 Pedras MS, Gadagi RS, Jha M, Sarma-Mamillapalle VK. Detoxification of the phytoalexin brassinin by isolates of Leptosphaeria maculans pathogenic on brown mustard involves an inducible hydrolase. Phytochemistry. 68: 1572-8. PMID 17467751 DOI: 10.1016/J.Phytochem.2007.03.020  0.452
2007 Pedras MS, Zheng QA, Sarwar MG. Efficient synthesis of brussalexin A, a remarkable phytoalexin from Brussels sprouts. Organic & Biomolecular Chemistry. 5: 1167-9. PMID 17406713 DOI: 10.1039/B702156A  0.416
2007 Pedras MS, Zheng QA, Gadagi RS. The first naturally occurring aromatic isothiocyanates, rapalexins A and B, are cruciferous phytoalexins. Chemical Communications (Cambridge, England). 368-70. PMID 17220973 DOI: 10.1039/B615424G  0.451
2006 Pedras MS, Suchý M. Metabolism of the crucifer phytoalexins wasalexin A and B in the plant pathogenic fungus Leptosphaeria maculans. Organic & Biomolecular Chemistry. 4: 3526-35. PMID 17036150 DOI: 10.1039/B609367A  0.506
2006 Pedras MS, Sarwar MG, Suchy M, Adio AM. The phytoalexins from cauliflower, caulilexins A, B and C: isolation, structure determination, syntheses and antifungal activity. Phytochemistry. 67: 1503-9. PMID 16806330 DOI: 10.1016/J.Phytochem.2006.05.020  0.398
2006 Pedras MS, Hossain M. Metabolism of crucifer phytoalexins in Sclerotinia sclerotiorum: detoxification of strongly antifungal compounds involves glucosylation. Organic & Biomolecular Chemistry. 4: 2581-90. PMID 16791322 DOI: 10.1039/B604400J  0.482
2006 Pedras MS, Okinyo DP. En route to erucalexin: a unique rearrangement in the crucifer phytoalexin biosynthetic pathway. Chemical Communications (Cambridge, England). 1848-50. PMID 16622504 DOI: 10.1039/B602189A  0.361
2006 Pedras MS, Suchy M, Ahiahonu PW. Unprecedented chemical structure and biomimetic synthesis of erucalexin, a phytoalexin from the wild crucifer Erucastrum gallicum. Organic & Biomolecular Chemistry. 4: 691-701. PMID 16467943 DOI: 10.1039/B515331J  0.746
2006 Pedras MS, Suchy M. Design, synthesis, and antifungal activity of inhibitors of brassilexin detoxification in the plant pathogenic fungus Leptosphaeria maculans. Bioorganic & Medicinal Chemistry. 14: 714-23. PMID 16202609 DOI: 10.1016/J.Bmc.2005.08.053  0.416
2005 Pedras MS, Yu Y, Liu J, Tandron-Moya YA. Metabolites produced by the phytopathogenic fungus Rhizoctonia solani: isolation, chemical structure determination, syntheses and bioactivity. Zeitschrift FüR Naturforschung. C, Journal of Biosciences. 60: 717-22. PMID 16320614 DOI: 10.1515/Znc-2005-9-1010  0.373
2005 Pedras MS, Jha M, Okeola OG. Camalexin induces detoxification of the phytoalexin brassinin in the plant pathogen Leptosphaeria maculans. Phytochemistry. 66: 2609-16. PMID 16266734 DOI: 10.1016/J.Phytochem.2005.09.013  0.435
2005 Pedras MS, Suchy M. Detoxification pathways of the phytoalexins brassilexin and sinalexin in Leptosphaeria maculans: isolation and synthesis of the elusive intermediate 3-formylindolyl-2-sulfonic acid. Organic & Biomolecular Chemistry. 3: 2002-7. PMID 15889184 DOI: 10.1039/B501907A  0.464
2005 Pedras MS, Chumala PB, Venkatesham U. New sesquiterpenic phytotoxins establish unprecedented relationship between different groups of blackleg fungal isolates. Bioorganic & Medicinal Chemistry. 13: 2469-75. PMID 15755649 DOI: 10.1016/J.Bmc.2005.01.040  0.364
2005 Pedras MS, Ahiahonu PW. Metabolism and detoxification of phytoalexins and analogs by phytopathogenic fungi. Phytochemistry. 66: 391-411. PMID 15694450 DOI: 10.1016/J.Phytochem.2004.12.032  0.752
2005 Pedras MS, Chumala PB. Phomapyrones from blackleg causing phytopathogenic fungi: isolation, structure determination, biosyntheses and biological activity. Phytochemistry. 66: 81-7. PMID 15649514 DOI: 10.1016/J.Phytochem.2004.10.011  0.41
2004 Pedras MS, Ahiahonu PW. Phytotoxin production and phytoalexin elicitation by the phytopathogenic fungus Sclerotinia sclerotiorum. Journal of Chemical Ecology. 30: 2163-79. PMID 15672663 DOI: 10.1023/B:Joec.0000048781.72203.6C  0.742
2004 Pedras MS, Chumala PB, Quail JW. Chemical mediators: the remarkable structure and host-selectivity of depsilairdin, a sesquiterpenic depsipeptide containing a new amino acid. Organic Letters. 6: 4615-7. PMID 15548089 DOI: 10.1021/Ol0478786  0.377
2004 Pedras MS, Ahiahonu PW, Hossain M. Detoxification of the cruciferous phytoalexin brassinin in Sclerotinia sclerotiorum requires an inducible glucosyltransferase. Phytochemistry. 65: 2685-94. PMID 15464156 DOI: 10.1016/J.Phytochem.2004.08.033  0.754
2004 Pedras MS, Montaut S, Suchy M. Phytoalexins from the crucifer rutabaga: structures, syntheses, biosyntheses, and antifungal activity. The Journal of Organic Chemistry. 69: 4471-6. PMID 15202903 DOI: 10.1021/Jo049648A  0.477
2004 Pedras MS, Liu J. Designer phytoalexins: probing camalexin detoxification pathways in the phytopathogen Rhizoctonia solani. Organic & Biomolecular Chemistry. 2: 1070-6. PMID 15034631 DOI: 10.1039/B400031E  0.394
2004 Pedras MS, Montaut S. The biosynthesis of crucifer phytoalexins: unprecedented incorporation of a 1-methoxyindolyl precursor. Chemical Communications (Cambridge, England). 452-3. PMID 14765254 DOI: 10.1039/B313762G  0.33
2003 Pedras MS, Chumala PB, Suchy M. Phytoalexins from Thlaspi arvense, a wild crucifer resistant to virulent Leptosphaeria maculans: structures, syntheses and antifungal activity. Phytochemistry. 64: 949-56. PMID 14561510  0.336
2003 Pedras MS, Montaut S. Probing crucial metabolic pathways in fungal pathogens of crucifers: biotransformation of indole-3-acetaldoxime, 4-hydroxyphenylacetaldoxime, and their metabolites. Bioorganic & Medicinal Chemistry. 11: 3115-20. PMID 12818674 DOI: 10.1016/S0968-0896(03)00241-4  0.477
2003 Pedras MS, Ismail N, Quail JW, Boyetchko SM. Structure, chemistry, and biological activity of pseudophomins A and B, new cyclic lipodepsipeptides isolated from the biocontrol bacterium Pseudomonas fluorescens. Phytochemistry. 62: 1105-14. PMID 12591264 DOI: 10.1016/S0031-9422(02)00617-9  0.442
2003 Pedras M, Jha M, Ahiahonu P. The Synthesis and Biosynthesis of Phytoalexins Produced by Cruciferous Plants Current Organic Chemistry. 7: 1635-1647. DOI: 10.2174/1385272033486242  0.31
2002 Pedras MS, Ahiahonu PW. Probing the phytopathogenic stem rot fungus with phytoalexins and analogues: unprecedented glucosylation of camalexin and 6-methoxycamalexin. Bioorganic & Medicinal Chemistry. 10: 3307-12. PMID 12150877 DOI: 10.1016/S0968-0896(02)00208-0  0.748
2002 Pedras MS, Nycholat CM, Montaut S, Xu Y, Khan AQ. Chemical defenses of crucifers: elicitation and metabolism of phytoalexins and indole-3-acetonitrile in brown mustard and turnip. Phytochemistry. 59: 611-25. PMID 11867093 DOI: 10.1016/S0031-9422(02)00026-2  0.709
2002 Pedras MS, Irina Zaharia L, Ward DE. The destruxins: synthesis, biosynthesis, biotransformation, and biological activity. Phytochemistry. 59: 579-96. PMID 11867090 DOI: 10.1016/S0031-9422(02)00016-X  0.414
2001 Pedras MS, Montaut S, Xu Y, Khan AQ, Loukaci A. Assembling the biosynthetic puzzle of crucifer metabolites: indole-3-acetaldoxime is incorporated efficiently into phytoalexins but glucobrassicin is not. Chemical Communications (Cambridge, England). 1572-3. PMID 12240387 DOI: 10.1039/B103442C  0.331
2001 Ward DE, Gai Y, Lazny R, Pedras MS. Probing host-selective phytotoxicity: synthesis of destruxin B and several natural analogues. The Journal of Organic Chemistry. 66: 7832-40. PMID 11701043 DOI: 10.1021/Jo015953+  0.349
2001 Pedras MS, Zaharia IL, Gai Y, Zhou Y, Ward DE. In planta sequential hydroxylation and glycosylation of a fungal phytotoxin: Avoiding cell death and overcoming the fungal invader. Proceedings of the National Academy of Sciences of the United States of America. 98: 747-52. PMID 11149945 DOI: 10.1073/pnas.021394998  0.339
2000 Pedras MS, Zaharia IL. Sinalbins A and B, phytoalexins from Sinapis alba: elicitation, isolation, and synthesis. Phytochemistry. 55: 213-6. PMID 11142844 DOI: 10.1016/S0031-9422(00)00277-6  0.438
2000 Pedras MS, Okanga FI, Zaharia IL, Khan AQ. Phytoalexins from crucifers: synthesis, biosynthesis, and biotransformation. Phytochemistry. 53: 161-76. PMID 10680168 DOI: 10.1016/S0031-9422(99)00494-X  0.481
2000 Pedras MS, Khan AQ. Biotransformation of the phytoalexin camalexin by the phytopathogen Rhizoctonia solani. Phytochemistry. 53: 59-69. PMID 10656409 DOI: 10.1016/S0031-9422(99)00479-3  0.46
2000 Pedras MS, Okanga FI. Metabolism of analogs of the phytoalexin brassinin by plant pathogenic fungi Canadian Journal of Chemistry. 78: 338-346. DOI: 10.1139/v00-024  0.326
1999 Ward DE, Vázquez A, Pedras MS. Probing Host-Selective Phytotoxicity: Synthesis and Biological Activity of Phomalide, Isophomalide, and Dihydrophomalide. The Journal of Organic Chemistry. 64: 1657-1666. PMID 11674233 DOI: 10.1021/Jo982376P  0.371
1999 Pedras MS, Erosa-López CC, Quail JW, Taylor JL. Phomalairdenone: a new host-selective phytotoxin from a virulent type of the blackleg fungus Phoma lingam. Bioorganic & Medicinal Chemistry Letters. 9: 3291-4. PMID 10612587 DOI: 10.1016/S0960-894X(99)00602-2  0.338
1999 Pedras MS, Sorensen JL, Okanga FI, Zaharia IL. Wasalexins A and B, new phytoalexins from wasabi: isolation, synthesis, and antifungal activity. Bioorganic & Medicinal Chemistry Letters. 9: 3015-20. PMID 10571166 DOI: 10.1016/S0960-894X(99)00523-5  0.432
1999 Pedras MS, Okanga FI. Strategies of cruciferous pathogenic fungi: detoxification of the phytoalexin cyclobrassinin by mimicry. Journal of Agricultural and Food Chemistry. 47: 1196-202. PMID 10552437  0.332
1998 Pedras MS, Smith KC, Taylor JL. Production of 2,5-dioxopiperazine by a new isolate type of the blackleg fungus Phoma lingam. Phytochemistry. 49: 1575-1577. PMID 11711067 DOI: 10.1016/S0031-9422(98)00271-4  0.344
1996 Ward DE, Vazquez A, Pedras MS. Understanding Host-Selective Phytotoxicity: Synthesis and Biological Discrimination of Phomalide and Its (Z)-Isomer. The Journal of Organic Chemistry. 61: 8008-8009. PMID 11667782 DOI: 10.1021/Jo961661A  0.312
1987 Ayer WA, Pedras MS, Ward DE. Metabolites produced by the Scleroderris canker fungus, Gremmeniellaabietina. Part 4. Biosynthetic studies Canadian Journal of Chemistry. 65: 760-764. DOI: 10.1139/V87-129  0.48
1987 Ayer WA, Pedras MS. Metabolites produced by the Scleroderris canker fungus, Gremmeniellaabietina. Part 3. Some further metabolites Canadian Journal of Chemistry. 65: 754-759. DOI: 10.1139/V87-128  0.513
1987 Ayer WA, Hoyano Y, Pedras MS, Clardy J, Arnold E. Metabolites produced by the scleroderris canker fungus, Gremmeniellaabietina. Part 2. The structure of scleroderolide Canadian Journal of Chemistry. 65: 748-753. DOI: 10.1139/V87-127  0.489
1986 Ayer WA, Hoyano Y, Pedras MS, Altena Iv. Metabolites produced by the Scleroderris canker fungus, Gremmeniellaabietina. Part 1 Canadian Journal of Chemistry. 64: 1585-1589. DOI: 10.1139/V86-262  0.52
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