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Hygrolansamycins A-D, O-Heterocyclic Macrolides from Streptomyces sp. KCB17JA11.


ABSTRACT: Six ansamycin derivatives were isolated from the culture broth of Streptomyces sp. KCB17JA11, including four new hygrolansamycins A-D (1-4) and known congeners divergolide O (5) and hygrocin C (6). Compounds 1-5 featured an unusual six-membered O-heterocyclic moiety. The isolation workflow was guided by a Molecular Networking-based dereplication strategy. The structures of 1-4 were elucidated using NMR and HRESIMS experiments, and the absolute configuration was established by the Mosher's method. Compound 2 exhibited mild cytotoxicity against five cancer cell lines with IC50 values ranging from 24.60 ± 3.37 μM to 49.93 ± 4.52 μM.

SUBMITTER: Jang JP 

PROVIDER: S-EPMC9668088 | biostudies-literature | 2022 Oct

REPOSITORIES: biostudies-literature

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Hygrolansamycins A-D, <i>O</i>-Heterocyclic Macrolides from <i>Streptomyces</i> sp. KCB17JA11.

Jang Jun-Pil JP   Lee Byeongsan B   Heo Kyung Taek KT   Oh Tae Hoon TH   Lee Hyeok-Won HW   Ko Sung-Kyun SK   Hwang Bang Yeon BY   Jang Jae-Hyuk JH   Hong Young-Soo YS  

Journal of microbiology and biotechnology 20220905 10


Six ansamycin derivatives were isolated from the culture broth of <i>Streptomyces</i> sp. KCB17JA11, including four new hygrolansamycins A-D (1-4) and known congeners divergolide O (5) and hygrocin C (6). Compounds 1-5 featured an unusual six-membered <i>O</i>-heterocyclic moiety. The isolation workflow was guided by a Molecular Networking-based dereplication strategy. The structures of 1-4 were elucidated using NMR and HRESIMS experiments, and the absolute configuration was established by the M  ...[more]

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