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Bioactive Bis(indole) Alkaloids from a Spongosorites sp. Sponge

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dc.contributor.authorPark, Jae Sung-
dc.contributor.authorCho, Eunji-
dc.contributor.authorHwang, Ji-Yeon-
dc.contributor.authorPark, Sung Chul-
dc.contributor.authorChung, Beomkoo-
dc.contributor.authorKwon, Oh-Seok-
dc.contributor.authorSim, Chung J.-
dc.contributor.authorOh, Dong-Chan-
dc.contributor.authorOh, Ki-Bong-
dc.contributor.authorShin, Jongheon-
dc.date.accessioned2024-08-08T01:24:52Z-
dc.date.available2024-08-08T01:24:52Z-
dc.date.created2021-05-24-
dc.date.created2021-05-24-
dc.date.issued2021-01-
dc.identifier.citationMarine Drugs, Vol.19 No.1, p. 3-
dc.identifier.issn1660-3397-
dc.identifier.urihttps://hdl.handle.net/10371/205816-
dc.description.abstractSix new bis(indole) alkaloids (1-6) along with eight known ones of the topsentin class were isolated from a Spongosorites sp. sponge of Korea. Based on the results of combined spectroscopic analyses, the structures of spongosoritins A-D (1-4) were determined to possess a 2-methoxy-1-imidazole-5-one core connecting the indole moieties, and these were linked by a linear urea bridge for spongocarbamides A (5) and B (6). The absolute configurations of spongosoritins were assigned by electronic circular dichroism (ECD) computation. The new compounds exhibited moderate inhibition against transpeptidase sortase A and weak inhibition against human pathogenic bacteria and A549 and K562 cancer cell lines.-
dc.language영어-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.titleBioactive Bis(indole) Alkaloids from a Spongosorites sp. Sponge-
dc.typeArticle-
dc.identifier.doi10.3390/md19010003-
dc.citation.journaltitleMarine Drugs-
dc.identifier.wosid000610379800001-
dc.identifier.scopusid2-s2.0-85099116271-
dc.citation.number1-
dc.citation.startpage3-
dc.citation.volume19-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorOh, Dong-Chan-
dc.contributor.affiliatedAuthorOh, Ki-Bong-
dc.contributor.affiliatedAuthorShin, Jongheon-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordAuthorSpongosorites sp-
dc.subject.keywordAuthorsponge-
dc.subject.keywordAuthorbis(indole) alkaloids-
dc.subject.keywordAuthorspongosoritins-
dc.subject.keywordAuthorspongocarbamides-
dc.subject.keywordAuthortopsentin-
dc.subject.keywordAuthorsortase A inhibition-
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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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