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Callyazepin and (3R)-methylazacyclodecane, nitrogenous macrocycles from a callyspongia sp sponge

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dc.contributor.authorKim, Chang-Kwon-
dc.contributor.authorWoo, Jung-Kyun-
dc.contributor.authorLee, Yeon-Ju-
dc.contributor.authorLee, Hyi-Seung-
dc.contributor.authorSim, Chung J.-
dc.contributor.authorOh, Dong-Chan-
dc.contributor.authorOh, Ki-Bong-
dc.contributor.authorShin, Jongheon-
dc.date.accessioned2024-08-08T01:37:07Z-
dc.date.available2024-08-08T01:37:07Z-
dc.date.created2017-11-15-
dc.date.created2017-11-15-
dc.date.issued2016-04-
dc.identifier.citationJournal of Natural Products, Vol.79 No.4, pp.1179-1183-
dc.identifier.issn0163-3864-
dc.identifier.urihttps://hdl.handle.net/10371/206978-
dc.description.abstractCallyazepin (1) and (3R)-methylazacyclodecane (2), nitrogenous macrocycles, were isolated from a tropical Callyspongia sp. sponge. The combined spectroscopic analyses revealed that the structure of 1 is a bicyclic azepane ammonium salt of a novel structural class derived from mixed biogenetic origins. The configuration of the whole molecule and the conformation of the formamide group were assigned by proton-proton coupling constants, a NOESY analysis, and the application of the phenylglycine methyl ester method. The structure of 2 was identified using combined spectroscopic analyses and ECD measurements. These compounds exhibited moderate cytotoxic activities against the K562 and A549 cell lines.-
dc.language영어-
dc.publisherAmerican Chemical Society-
dc.titleCallyazepin and (3R)-methylazacyclodecane, nitrogenous macrocycles from a callyspongia sp sponge-
dc.typeArticle-
dc.identifier.doi10.1021/acs.jnatprod.5b01078-
dc.citation.journaltitleJournal of Natural Products-
dc.identifier.wosid000374915800066-
dc.identifier.scopusid2-s2.0-84967319397-
dc.citation.endpage1183-
dc.citation.number4-
dc.citation.startpage1179-
dc.citation.volume79-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorOh, Dong-Chan-
dc.contributor.affiliatedAuthorOh, Ki-Bong-
dc.contributor.affiliatedAuthorShin, Jongheon-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusMARINE NATURAL-PRODUCTS-
dc.subject.keywordPlusABSOLUTE-CONFIGURATION-
dc.subject.keywordPlusHALICLONA-TULEARENSIS-
dc.subject.keywordPlusCIRCULAR-DICHROISM-
dc.subject.keywordPlusDNP DERIVATIVES-
dc.subject.keywordPlusRENIERA-SARAI-
dc.subject.keywordPlusAMINO-ACIDS-
dc.subject.keywordPlusHALICLORENSIN-
dc.subject.keywordPlusMETABOLITES-
dc.subject.keywordPlusHALITULIN-
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  • College of Pharmacy
  • Department of Manufacturing Pharmacy
Research Area Chemical biology of natural products, Drug discovery from microbial natural products, Study of insect-microbial symbiosis, 미생물 유래 생리활성 천연물 발굴, 천연물 구조 분석

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