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Salternamides A-D from a Halophilic Streptomyces sp. Actinobacterium

Cited 34 time in Web of Science Cited 39 time in Scopus
Authors

Kim, Seong-Hwan; Shin, Yoonho; Lee, So-Hyoung; Oh, Ki-Bong; Lee, Sang Kook; Shin, Jongheon; Oh, Dong-Chan

Issue Date
2015-04
Publisher
American Chemical Society
Citation
Journal of Natural Products, Vol.78 No.4, pp.836-843
Abstract
Salternamides A-D (1-4), the first secondary metabolites discovered from saltern-derived actinomycetes, were isolated from a halophilic Streptomyces strain isolated from a saltern on Shinui Island in the Republic of Korea. The planar structures of the salternamides, which are new members of the manumycin family, were elucidated by a combination of spectroscopic analyses. The absolute configurations of the salternamides were determined by chemical and spectroscopic methods, including the modified Moshers method, J-based configuration analysis, and circular dichroism spectroscopy. Salternamide A (1), which is the first chlorinated compound in the manumycin family, exhibited potent cytotoxicity against a human colon cancer cell line (HCT116) and a gastric cancer cell line (SNU638) with submicromolar IC50 values. Salternamides A and D were also determined to be weak Na+/K+ ATPase inhibitors.
ISSN
0163-3864
URI
https://hdl.handle.net/10371/207252
DOI
https://doi.org/10.1021/acs.jnatprod.5b00002
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  • College of Pharmacy
  • Department of Manufacturing Pharmacy
Research Area Chemical biology of natural products, Drug discovery from microbial natural products, Study of insect-microbial symbiosis, 미생물 유래 생리활성 천연물 발굴, 천연물 구조 분석

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