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

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 guide...

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Autores principales: Jang, Jun-Pil, Lee, Byeongsan, Heo, Kyung Taek, Oh, Tae Hoon, Lee, Hyeok-Won, Ko, Sung-Kyun, Hwang, Bang Yeon, Jang, Jae-Hyuk, Hong, Young-Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Microbiology and Biotechnology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668088/
https://www.ncbi.nlm.nih.gov/pubmed/36198661
http://dx.doi.org/10.4014/jmb.2206.06039
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author Jang, Jun-Pil
Lee, Byeongsan
Heo, Kyung Taek
Oh, Tae Hoon
Lee, Hyeok-Won
Ko, Sung-Kyun
Hwang, Bang Yeon
Jang, Jae-Hyuk
Hong, Young-Soo
author_facet Jang, Jun-Pil
Lee, Byeongsan
Heo, Kyung Taek
Oh, Tae Hoon
Lee, Hyeok-Won
Ko, Sung-Kyun
Hwang, Bang Yeon
Jang, Jae-Hyuk
Hong, Young-Soo
author_sort Jang, Jun-Pil
collection PubMed
description 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 IC(50) values ranging from 24.60 ± 3.37 μM to 49.93 ± 4.52 μM.
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spelling pubmed-96680882022-12-13 Hygrolansamycins A-D, O-Heterocyclic Macrolides from Streptomyces sp. KCB17JA11 Jang, Jun-Pil Lee, Byeongsan Heo, Kyung Taek Oh, Tae Hoon Lee, Hyeok-Won Ko, Sung-Kyun Hwang, Bang Yeon Jang, Jae-Hyuk Hong, Young-Soo J Microbiol Biotechnol Research article 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 IC(50) values ranging from 24.60 ± 3.37 μM to 49.93 ± 4.52 μM. The Korean Society for Microbiology and Biotechnology 2022-10-28 2022-09-05 /pmc/articles/PMC9668088/ /pubmed/36198661 http://dx.doi.org/10.4014/jmb.2206.06039 Text en Copyright © 2022 by the authors. Licensee KMB. https://creativecommons.org/licenses/by/4.0/This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research article
Jang, Jun-Pil
Lee, Byeongsan
Heo, Kyung Taek
Oh, Tae Hoon
Lee, Hyeok-Won
Ko, Sung-Kyun
Hwang, Bang Yeon
Jang, Jae-Hyuk
Hong, Young-Soo
Hygrolansamycins A-D, O-Heterocyclic Macrolides from Streptomyces sp. KCB17JA11
title Hygrolansamycins A-D, O-Heterocyclic Macrolides from Streptomyces sp. KCB17JA11
title_full Hygrolansamycins A-D, O-Heterocyclic Macrolides from Streptomyces sp. KCB17JA11
title_fullStr Hygrolansamycins A-D, O-Heterocyclic Macrolides from Streptomyces sp. KCB17JA11
title_full_unstemmed Hygrolansamycins A-D, O-Heterocyclic Macrolides from Streptomyces sp. KCB17JA11
title_short Hygrolansamycins A-D, O-Heterocyclic Macrolides from Streptomyces sp. KCB17JA11
title_sort hygrolansamycins a-d, o-heterocyclic macrolides from streptomyces sp. kcb17ja11
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668088/
https://www.ncbi.nlm.nih.gov/pubmed/36198661
http://dx.doi.org/10.4014/jmb.2206.06039
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