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Cytotoxic Indolocarbazoles From a Marine-Derived Streptomyces Sp. OUCMDZ-5380.


ABSTRACT: Under the guidance of global natural product social molecular networking, three new indolocarbazoles named streptocarbazoles F-H (1-3), along with staurosporine (4) were isolated from the marine-derived Streptomyces sp. OUCMDZ-5380. Structures of streptocarbazoles F-H were, respectively, determined as N-demethyl-N-hexanoylstaurosporine (1), N-demethyl-N-(2-methyl-3-methoxypyridin-4-yl) staurosporine staurosporine (2), and 4-(N-demethylstaurosporine-N-yl)-1,2-dimethyl-3-methoxypyridinium (3) by spectroscopic analysis and electronic circular dichroism comparison with staurosporine. Compared with staurosporine (4), streptocarbazoles F-H (1-3) showed a selective antiproliferation of the acute myeloid leukemia cell line MV4-11 with the IC50 values of 0.81, 0.55, and 1.88 μM, respectively.

SUBMITTER: Cui T 

PROVIDER: S-EPMC9315148 | biostudies-literature | 2022

REPOSITORIES: biostudies-literature

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Cytotoxic Indolocarbazoles From a Marine-Derived <i>Streptomyces</i> Sp. OUCMDZ-5380.

Cui Tongxu T   Lin Simin S   Wang Zizhen Z   Fu Peng P   Wang Cong C   Zhu Weiming W  

Frontiers in microbiology 20220712


Under the guidance of global natural product social molecular networking, three new indolocarbazoles named streptocarbazoles F-H (<b>1</b>-<b>3</b>), along with staurosporine (<b>4</b>) were isolated from the marine-derived <i>Streptomyces</i> sp. OUCMDZ-5380. Structures of streptocarbazoles F-H were, respectively, determined as <i>N</i>-demethyl-<i>N</i>-hexanoylstaurosporine (<b>1</b>), <i>N</i>-demethyl-<i>N</i>-(2-methyl-3-methoxypyridin-4-yl) staurosporine staurosporine (<b>2</b>), and 4-(<  ...[more]

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