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Varioloid A, a new indolyl-6,10b-dihydro-5aH-[1]benzofuro[2,3-b]indole derivative from the marine alga-derived endophytic fungus Paecilomyces variotii EN-291.


ABSTRACT: A new indolyl-6,10b-dihydro-5aH-[1]benzofuro[2,3-b]indole derivative, varioloid A (1), was isolated from the marine alga-derived endophytic fungus Paecilomyces variotii EN-291. Its structure was elucidated on the basis of extensive analysis of 1D and 2D NMR data and the absolute configuration was determined by time-dependent density functional theory-electronic circular dichroism (TDDFT-ECD) calculations. A similar compound, whose planar structure was previously described but the relative and absolute configurations and 13C NMR data were not reported, was also identified and was tentatively named as varioloid B (2). Both compounds 1 and 2 exhibited cytotoxicity against A549, HCT116, and HepG2 cell lines, with IC50 values ranging from 2.6 to 8.2 µg/mL.

SUBMITTER: Zhang P 

PROVIDER: S-EPMC5082447 | biostudies-other | 2016

REPOSITORIES: biostudies-other

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Varioloid A, a new indolyl-6,10b-dihydro-5a<i>H</i>-[1]benzofuro[2,3-<i>b</i>]indole derivative from the marine alga-derived endophytic fungus <i>Paecilomyces variotii</i> EN-291.

Zhang Peng P   Li Xiao-Ming XM   Mao Xin-Xin XX   Mándi Attila A   Kurtán Tibor T   Wang Bin-Gui BG  

Beilstein journal of organic chemistry 20160909


A new indolyl-6,10b-dihydro-5a<i>H</i>-[1]benzofuro[2,3-<i>b</i>]indole derivative, varioloid A (<b>1</b>), was isolated from the marine alga-derived endophytic fungus <i>Paecilomyces variotii</i> EN-291. Its structure was elucidated on the basis of extensive analysis of 1D and 2D NMR data and the absolute configuration was determined by time-dependent density functional theory-electronic circular dichroism (TDDFT-ECD) calculations. A similar compound, whose planar structure was previously descr  ...[more]

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