Pyrimidine Nucleosides, Benzoic Acid Derivative, and Bipyridine From the Marine‐Derived <i>Streptomyces</i> Sp. DS52

Fourteen new compounds were isolated from marine-derived Streptomyces sp. DS52, including 12 pyrimidine nucleosides (1-12), 1 benzoic acid derivative (13), and 1 dipyridine derivative (14). Additionally, 28 known compounds (15-42) were identified. The structures of all compounds were elucidated through extensive analysis of nuclear magnetic resonance spectroscopic and high-resolution electrospray ionization mass spectroscopy data. Electronic circular dichroism (ECD) calculations were employed to investigate the configurations of compounds 1, 2, and 4-13. Bioactivity evaluations of all of the compounds showed that compound 41 exhibited significant cytotoxicity against the HCT-116 and MDA-MB-231 human cancer cell lines with IC<sub>50</sub> values of 0.73 ± 0.06 and 1.11 ± 0.06 µM, respectively. Notably, compounds 6, 7, 9, 11, 15, 33-38, 41, and 42 exhibited cytotoxicity against HCT-116 human colon cancer cell lines and MDA-MB-231 human breast cancer cell lines, with IC<sub>50</sub> values ranging from 0.73 ± 0.06 to 17.44 ± 0.53 µM and from 1.11 ± 0.06 to 18.51 ± 3.07 µM, respectively.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2024-11-27
DOI
https://doi.org/10.1002/cbdv.202402322
Citations
1
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
0.25
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Pyrimidine Nucleosides, Benzoic Acid Derivative, and Bipyridine From the Marine‐Derived Streptomyces Sp. DS52

Jiebin Fang, Zhongjun Ma, Shuang Chen, Yun Huang et al.
1 citations
Chemistry & Biodiversity
Click Chemistry and Applications
0.25
article

Pyrimidine Nucleosides, Benzoic Acid Derivative, and Bipyridine From the Marine‐Derived Streptomyces Sp. DS52

Jiebin Fang, Zhongjun Ma, Shuang Chen, Yun Huang, Xia Mao
article en
1 citations

Abstract

Fourteen new compounds were isolated from marine-derived Streptomyces sp. DS52, including 12 pyrimidine nucleosides (1-12), 1 benzoic acid derivative (13), and 1 dipyridine derivative (14). Additionally, 28 known compounds (15-42) were identified. The structures of all compounds were elucidated through extensive analysis of nuclear magnetic resonance spectroscopic and high-resolution electrospray ionization mass spectroscopy data. Electronic circular dichroism (ECD) calculations were employed to investigate the configurations of compounds 1, 2, and 4-13. Bioactivity evaluations of all of the compounds showed that compound 41 exhibited significant cytotoxicity against the HCT-116 and MDA-MB-231 human cancer cell lines with IC<sub>50</sub> values of 0.73 ± 0.06 and 1.11 ± 0.06 µM, respectively. Notably, compounds 6, 7, 9, 11, 15, 33-38, 41, and 42 exhibited cytotoxicity against HCT-116 human colon cancer cell lines and MDA-MB-231 human breast cancer cell lines, with IC<sub>50</sub> values ranging from 0.73 ± 0.06 to 17.44 ± 0.53 µM and from 1.11 ± 0.06 to 18.51 ± 3.07 µM, respectively.

Chemistry & BiodiversityVol. 22(4)
Zhejiang Ocean University (CN), Zhejiang University (CN)
Life below water
Openalex Percentile: Top 46%
Click Chemistry and Applications
0.25
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