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dc.contributor.authorKıran, İsmail
dc.contributor.authorDurceylan, Zeynep
dc.contributor.authorKırımer, Neşe
dc.contributor.authorBaşer, K. Hüsnü Can
dc.contributor.authorNoma, Yoshiaki
dc.contributor.authorDemirci, Fatih
dc.date.accessioned2019-10-19T14:15:20Z
dc.date.available2019-10-19T14:15:20Z
dc.date.issued2010
dc.identifier.issn1934-578X
dc.identifier.urihttps://hdl.handle.net/11421/12775
dc.descriptionWOS: 000276598500003en_US
dc.descriptionPubMed ID: 20433062en_US
dc.description.abstractIncubation of a-cedrol and caryophyllene oxide with Neurospora crassa afforded 12 beta-hydroxy cedrol, 10 alpha-hydroxy cedrol, and 3 beta-hydroxy cedrol, and 12 beta-hydroxy caryophyllene oxide as major metabolites, respectively. The antibacterial and radical scavenging activities of the metabolites were evaluated in vitro using broth microdilution and bioauthographic techniques. However, no significant antibacterial and antioxidant activities were observed when compared with those of standard substances.en_US
dc.language.isoengen_US
dc.publisherNatural Products Incen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectNeurospora Crassaen_US
dc.subjectBiotransformationen_US
dc.subjectCaryophyllene Oxideen_US
dc.subjectAlpha-Cedrolen_US
dc.subjectAntibacterial Activityen_US
dc.subjectRadical Scavenging Activityen_US
dc.titleBiotransformation of alpha-Cedrol and Caryophyllene Oxide by the Fungus Neurospora crassaen_US
dc.typearticleen_US
dc.relation.journalNatural Product Communicationsen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Farmakognozi Anabilim Dalıen_US
dc.identifier.volume5en_US
dc.identifier.issue4en_US
dc.identifier.startpage515en_US
dc.identifier.endpage518en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorKırımer, Neşe
dc.contributor.institutionauthorBaşer, K. Hüsnü Can
dc.contributor.institutionauthorDemirci, Fatih


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