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Isolation of Scalarane-Type Sesterterpenoids from the Marine Sponge Dysidea sp. and Stereochemical Reassignment of 12-epi-Phyllactone D/E.


ABSTRACT: The chemical investigation of the marine sponge Dysidea sp., which was collected from Bohol province in the Philippines, resulted in the identification of 15 new scalarane-type sesterterpenoids (1-14, 16), together with 15 known compounds. The chemical structures of the new compounds were elucidated based on NMR spectroscopy and HRMS. The structure of 12-epi-phyllactone D/E (15) isolated during this study was originally identified in 2007. However, careful inspection of our experimental 13C NMR spectrum revealed considerable discrepancies with the reported data at C-9, C-12, C-14, and C-23, leading to the correction of the reported compound to the C-12 epimer of 15, phyllactone D/E. The biological properties of compounds 1-16 were evaluated using the MDA-MB-231 cancer cell line. Compound 7, which bears a pentenone E-ring, exhibits significant cytotoxicity with a GI50 value of 4.21 μM.

SUBMITTER: Shin AY 

PROVIDER: S-EPMC8624410 | biostudies-literature | 2021 Nov

REPOSITORIES: biostudies-literature

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Isolation of Scalarane-Type Sesterterpenoids from the Marine Sponge <i>Dysidea</i> sp. and Stereochemical Reassignment of 12-<i>epi</i>-Phyllactone D/E.

Shin A-Young AY   Son Arang A   Choi Changhoon C   Lee Jihoon J  

Marine drugs 20211109 11


The chemical investigation of the marine sponge <i>D</i><i>ysidea</i> sp., which was collected from Bohol province in the Philippines, resulted in the identification of 15 new scalarane-type sesterterpenoids (<b>1</b>-<b>1</b><b>4</b>, <b>1</b><b>6</b>), together with 15 known compounds. The chemical structures of the new compounds were elucidated based on NMR spectroscopy and HRMS. The structure of 12-<i>epi</i>-phyllactone D/E (<b>15</b>) isolated during this study was originally identified in  ...[more]

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