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A New Curvularin Glycoside and Its Cytotoxic and Antibacterial Analogues From Marine Actinomycete Pseudonocardia Sp. HS7

Xuewei Ye, Komal Anjum, Tengfei Song, Wenling Wang, Siran Yu, Haocai Huang, Xiao-Yuan Lian, Zhizhen Zhang

Nat Prod Res. 2016;30(10):1156-61.

PMID: 26119337

Abstract:

Five curvularin macrolides (1-5) were isolated from the cultured broth of marine actinomycete Pseudonocardia sp. HS7 that was obtained from the cloacal aperture of sea cucumber Holothuria moebii. The structures of these isolates were characterized as (11S,15R)-11-hydroxycurvularin (1), (11R,15R)-11-hydroxycurvularin (2), curvularin-7-O-α-D-glucopyranoside (3), trans-dehydrocurvularin (4) and curvularin (5) based on their NMR and HRESIMS data as well as chemical degradation. Compound 3 is a new macrolide with a rare α-D-glucopyranose substituent. Compounds 1-4, 5a and 5c (the acyl products of 5), suppressed the proliferation of all six tested cancer cell lines and 4 is the most active compound with IC50 values ranging from 0.59 to 3.39 μM. The 11-hydroxycurvularins 1 and 2 also showed antibacterial activity inhibiting the growth of Escherichia coli.

Chemicals Related in the Paper:

Catalog Number Product Name Structure CAS Number Price
AP10140702 Curvularin Curvularin 10140-70-2 Price
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