Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/49726
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dc.contributor.authorEmilie Adelinen_US
dc.contributor.authorClaudine Servyen_US
dc.contributor.authorSylvie Cortialen_US
dc.contributor.authorHélne Lévaiqueen_US
dc.contributor.authorJean Franois Gallarden_US
dc.contributor.authorMarie Thérse Martinen_US
dc.contributor.authorPascal Retailleauen_US
dc.contributor.authorBoonsom Bussabanen_US
dc.contributor.authorSaisamorn Lumyongen_US
dc.contributor.authorJamal Ouazzanien_US
dc.date.accessioned2018-09-04T04:06:11Z-
dc.date.available2018-09-04T04:06:11Z-
dc.date.issued2011-04-15en_US
dc.identifier.issn0960894Xen_US
dc.identifier.other2-s2.0-79953278003en_US
dc.identifier.other10.1016/j.bmcl.2011.02.063en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79953278003&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/49726-
dc.description.abstractSch-642305 is the major compound produced by the endophytic fungi Phomopsis sp. CMU-LMA. Incubation of Sch-642305 with Aspergillus ochraceus ATCC 1009 resting cells leads to three new derivatives through an oxido-reduction of the six-membered ring of the molecule. Reduction of the double bound leads to compound (1), which subsequently undergoes carbonyl reduction to (2) and ring hydroxylation to (3). According to the previously solved crystal structure of Sch-642305 coupled with1H NMR NOE correlation and the crystal structure of compound 1, the absolute configurations of the new derivatives were established. In contrast to the parent compound Sch-642305, compound (1) exhibits antimicrobial activity against Gram-negative bacteria. Furthermore, while all derivatives exhibit cytotoxic activity against various cancer cell lines, compound (2) achieved an IC50of 4 nM against human myelogenous leukemia K 562, compared to 20 nM for the parent Sch-642305. © 2011 Elsevier Ltd. All rights reserved.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleBiotransformation of natural compounds. Oxido-reduction of Sch-642305 by Aspergillus ochraceus ATCC 1009en_US
dc.typeJournalen_US
article.title.sourcetitleBioorganic and Medicinal Chemistry Lettersen_US
article.volume21en_US
article.stream.affiliationsInstitut de Chimie des Substances Naturellesen_US
article.stream.affiliationsChiang Mai Universityen_US
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