Isolation of Scalarane‐Type Sesterterpenoids from the Marine Sponge Dysidea sp. and Stereochemical Reassignment of 12‐epi‐phyllactone D/E SCIE SCOPUS

Cited 6 time in WEB OF SCIENCE Cited 5 time in Scopus
Title
Isolation of Scalarane‐Type Sesterterpenoids from the Marine Sponge Dysidea sp. and Stereochemical Reassignment of 12‐epi‐phyllactone D/E
Author(s)
Shin, A Young; Son, Arang; Choi, Changhoon; Lee, Jihoon
KIOST Author(s)
Shin, A Young(신아영)Lee, Ji Hoon(이지훈)
Alternative Author(s)
신아영; 이지훈
Publication Year
2021-11
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 mM.
ISSN
1660-3397
URI
https://sciwatch.kiost.ac.kr/handle/2020.kiost/41687
DOI
10.3390/md19110627
Bibliographic Citation
Marine Drugs, v.19, no.11, 2021
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
Dysidea; sesterterpenoid; scalarane; marine sponge; marine natural product; anticancer activity; stereochemistry reassignment
Type
Article
Language
English
Document Type
Article
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