4.7 Article

Baphicacanthcusines A-E, Bisindole Alkaloids from the Leaves of Baphicacanthus cusia (Nees) Bremek

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 85, Issue 13, Pages 8580-8587

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.0c00949

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Four pairs of stereoisomeric indole alkaloids, (+/-)-baphicacanthcusines A-D (1-4), and one new indole alkaloid, baphicacanthcusine E (5), together with nine known compounds were identified from the leaves of Baphicacanthus cusia. (+/-)-1 and -2 possess an unprecedented skeleton in which two indole moieties are bridged by a phenylpropane unit. (+/-)-3 represents the first natural dispiro-oxazolidinone bisoxindoles. The absolute configurations in 1-5 were assigned based on quantum chemical calculations, including the calculated chemical shift with DP4plus analysis, the calculated optical rotation values, and the calculated electronic circular dichroism spectra. A plausible biosynthetic pathway for 1-5 was proposed. Compounds (+/-)-1, (-)-2, and 11 exhibited cytotoxicity against MCF-7 cells with IC50 values of 20.0-78.5 mu M.

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