Cytotoxic rearranged angucycline glycosides from deep sea-derived Streptomyces lusitanus SCSIO LR32-Reference-Cited by-同舟云学术

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Cytotoxic rearranged angucycline glycosides from deep sea-derived Streptomyces lusitanus SCSIO LR32

Published:2017-02-22 Issue:7 Volume:70 Page:819-822
ISSN:0021-8820
Container-title:The Journal of Antibiotics
language:en
Short-container-title:J Antibiot

Author:

Zhu Xiangcheng,Duan Yanwen,Cui Zhaomeng,Wang Zhen,Li Zengxia,Zhang Yun,Ju Jianhua,Huang Hongbo

Publisher

Springer Science and Business Media LLC

Subject

Drug Discovery,Pharmacology

Link

https://www.nature.com/articles/ja201717.pdf

Reference15 articles.

1. Rohr, J. & Thiericke, R. Angucycline group antibiotics. Nat. Prod. Rep. 9, 103–137 (1992).

2. Kharel, M. K. et al. Angucyclines: biosynthesis, mode-of-action, new natural products, and synthesis. Nat. Prod. Rep. 29, 264–325 (2012).

3. Krohn, K. & Rohr, J. Angucyclines: total syntheses, new structures, and biosynthetic studies of an emerging new class of antibiotics. Top. Curr. Chem. 188, 127–195 (1997).

4. Huang, H. et al. Cytotoxic angucycline class glycosides from the deep sea actinomycete Streptomyces lusitanus SCSIO LR32. J. Nat. Prod. 75, 202–208 (2012).

5. Zhang, Y. et al. Identification of the grincamycin gene cluster unveils divergent roles for GcnQ in different hosts, tailoring the L-rhodinose moiety. Org. Lett. 15, 3254–3257 (2013).

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2. Deciphering the Glycosylation Steps in the Biosynthesis of P-1894B and Grincamycin Isolated from Marine-Derived Streptomyces lusitanus SCSIO LR32;Marine Drugs;2024-01-02

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4. Cytotoxic compounds from marine actinomycetes: sources, structures and bioactivity;Acta Materia Medica;2022-11-15

5. Integrated Metabolomic, Molecular Networking, and Genome Mining Analyses Uncover Novel Angucyclines From Streptomyces sp. RO-S4 Strain Isolated From Bejaia Bay, Algeria;Frontiers in Microbiology;2022-06-23

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