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dc.contributor.authorKei Ichi Ishidohen_US
dc.contributor.authorHiroshi Kinoshitaen_US
dc.contributor.authorYasuhiro Igarashien_US
dc.contributor.authorFumio Iharaen_US
dc.contributor.authorTakuya Nihiraen_US
dc.contributor.otherOsaka Universityen_US
dc.contributor.otherToyama Prefectural Universityen_US
dc.contributor.otherInstitute of Fruit Tree and Tea Science, NAROen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-11-09T03:11:24Z-
dc.date.available2018-11-09T03:11:24Z-
dc.date.issued2014-01-01en_US
dc.identifier.citationJournal of Antibiotics. Vol.67, No.6 (2014), 459-463en_US
dc.identifier.issn18811469en_US
dc.identifier.issn00218820en_US
dc.identifier.other2-s2.0-84903537170en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84903537170&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/34916-
dc.description.abstractVerlamelin and its new derivative (verlamelin B) were isolated from fermentation broth of entomopathogenic fungus Lecanicillium sp. HF627. As the structural elucidation of verlamelin so far was only preliminary, we studied and determined the absolute structure of these two compounds to be cyclo(5S-hydroxytetradecanoic acid-D-alloThr/Ser-D-Ala-L-Pro-L-Gln-D-Tyr-L-Val). This is the first study that precisely analyzed the structure of verlamelin. © 2014 Japan Antibiotics Research Association All rights reserve.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84903537170&origin=inwarden_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleCyclic lipodepsipeptides verlamelin A and B, isolated from entomopathogenic fungus Lecanicillium sp.en_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1038/ja.2014.22en_US
Appears in Collections:Scopus 2011-2015

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