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Retinestatin, a Polyol Polyketide from a Termite Nest-Derived Streptomyces sp.

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dc.contributor.authorHuynh, Thanh-Hau-
dc.contributor.authorKim, Hee Kyung-
dc.contributor.authorLee, Jayho-
dc.contributor.authorBan, Yeon Hee-
dc.contributor.authorJang, Yong-Joon-
dc.contributor.authorHeo, Bo Eun-
dc.contributor.authorNguyen, Thanh Quang-
dc.contributor.authorAn, Joon Soo-
dc.contributor.authorKwon, Yun-
dc.contributor.authorNam, Sang-Jip-
dc.contributor.authorJang, Jichan-
dc.contributor.authorOh, Ki-Bong-
dc.contributor.authorShin, Min-Kyoo-
dc.contributor.authorOh, Dong-Chan-
dc.date.accessioned2024-03-24T02:31:17Z-
dc.date.available2024-03-24T02:31:17Z-
dc.date.issued2024-03-
dc.identifier.issn0163-3864-
dc.identifier.issn1520-6025-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/70032-
dc.description.abstractA new polyol polyketide, named retinestatin (1), was obtained and characterized from the culture of a Streptomyces strain, which was isolated from a subterranean nest of the termite Reticulitermes speratus kyushuensis Morimoto. The planar structure of 1 was elucidated on the basis of the cumulative analysis of ultraviolet, infrared, mass spectrometry, and nuclear magnetic resonance spectroscopic data. The absolute configuration of 1 at 12 chiral centers was successfully assigned by employing a J-based configuration analysis in combination with ROESY correlations, a quantum mechanics-based computational approach to calculate NMR chemical shifts, and a 3 min flash esterification by Mosher’s reagents followed by NMR analysis. Biological evaluation of retinestatin (1) using an in vitro model of Parkinson’s disease revealed that 1 protected SH-SY5Y dopaminergic cells from MPP+-induced cytotoxicity, indicating its neuroprotective effects. © 2024 American Chemical Society and American Society of Pharmacognosy.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleRetinestatin, a Polyol Polyketide from a Termite Nest-Derived Streptomyces sp.-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acs.jnatprod.3c01043-
dc.identifier.scopusid2-s2.0-85187014098-
dc.identifier.wosid001180377200001-
dc.identifier.bibliographicCitationJournal of Natural Products, v.87, no.3, pp 591 - 599-
dc.citation.titleJournal of Natural Products-
dc.citation.volume87-
dc.citation.number3-
dc.citation.startPage591-
dc.citation.endPage599-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPlant Sciences-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPlant Sciences-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusABSOLUTE-CONFIGURATION-
dc.subject.keywordPlusMARINE ACTINOMYCETE-
dc.subject.keywordPlusPALYTOXIN-
dc.subject.keywordPlusSTEREOCHEMISTRY-
dc.subject.keywordPlusASSIGNMENT-
dc.subject.keywordPlusANTIBIOTICS-
dc.subject.keywordPlusAFLASTATIN-
dc.subject.keywordPlusOXIDANT-
dc.subject.keywordPlusMPP+-
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자연과학대학 > Division of Life Sciences > Journal Articles
학과간협동과정 > 바이오의료빅데이터학과 > Journal Articles

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