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Bacillamidins A?G from a Marine-Derived Bacillus pumilus.


ABSTRACT: Seven long-chain amides, including five previously undescribed bacillamidins A?E (1?5) and two previously reported synthetic analogs, bacillamidins F (6) and G (7), were isolated from extracts of the marine-derived Bacillus pumilus strain RJA1515. The structures of the new compounds were established by extensive analysis of 1D and 2D nuclear magnetic resonance (NMR) data as well as high resolution mass spectrometry (HRMS), and the absolute configurations of the stereogenic carbons of 1?4 were established by comparison of the calculated and the experimental electronic circular dichroism (ECD) spectra. The cytotoxic and antimicrobial activities of 1?7 were evaluated.

SUBMITTER: Zhou SY 

PROVIDER: S-EPMC6164710 | biostudies-literature | 2018 Sep

REPOSITORIES: biostudies-literature

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Bacillamidins A⁻G from a Marine-Derived <i>Bacillus pumilus</i>.

Zhou Si-Yu SY   Hu Yi-Jie YJ   Meng Fan-Cheng FC   Qu Shen-Yue SY   Wang Rui R   Andersen Raymond J RJ   Liao Zhi-Hua ZH   Chen Min M  

Marine drugs 20180911 9


Seven long-chain amides, including five previously undescribed bacillamidins A⁻E (<b>1</b>⁻<b>5</b>) and two previously reported synthetic analogs, bacillamidins F (<b>6</b>) and G (<b>7</b>), were isolated from extracts of the marine-derived <i>Bacillus pumilus</i> strain RJA1515. The structures of the new compounds were established by extensive analysis of 1D and 2D nuclear magnetic resonance (NMR) data as well as high resolution mass spectrometry (HRMS), and the absolute configurations of the  ...[more]

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