A pipecolic acid-rich branched cyclic depsipeptide ulleungamide C from a Streptomyces species induces G0/G1 cell cycle arrest in promyelocytic leukemia cells-Reference-Cited by-同舟云学术

A pipecolic acid-rich branched cyclic depsipeptide ulleungamide C from a Streptomyces species induces G0/G1 cell cycle arrest in promyelocytic leukemia cells

Published:2020-11-18 Issue:3 Volume:74 Page:181-189
ISSN:0021-8820
Container-title:The Journal of Antibiotics
language:en
Short-container-title:J Antibiot

Author:

Son Sangkeun,Jang Mina,Lee Byeongsan,Jang Jun-Pil,Hong Young-Soo^ORCID,Kim Bo Yeon^ORCID,Ko Sung-Kyun^ORCID,Jang Jae-Hyuk^ORCID,Ahn Jong Seog^ORCID

Funder

Korea Research Institute of Bioscience and Biotechnology

Publisher

Springer Science and Business Media LLC

Subject

Drug Discovery,Pharmacology

Link

http://www.nature.com/articles/s41429-020-00385-z.pdf

Reference17 articles.

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2. Ying H, et al. Expanding metabolic pathway for de novo biosynthesis of the chiral pharmaceutical intermediate L-pipecolic acid in Escherichia coli. Microb Cell Fact. 2017;16:52.

3. Matson JA, Bush JA. Sandramycin, a novel antitumor antibiotic produced by a Nocardioides sp. Production, isolation, characterization and biological properties. J Antibiot. 1989;42:1763–7.

4. Lee KK, Gloer JB, Scott JA, Malloch D. Petriellin A: a novel antifungal depsipeptide from the coprophilous fungus Petriella sordida. J Org Chem. 1995;60:5384–5.

5. Coello L, Reyes F, Martín MJ, Cuevas C, Fernandez R. Isolation and structures of pipecolidepsins A and B, cytotoxic cyclic depsipeptides from the Madagascan sponge Homophymia lamellose. J Nat Prod. 2014;77:298–303.

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