| Literature DB >> 34387477 |
Sojeong Kim1, Chang Wook Lee2, So-Yeon Park2, Ratnakar N Asolkar3, Haerin Kim1, Geum Jin Kim4, Song Jin Oh2, Youngbae Kim2, Eun-Young Lee5, Dong-Chan Oh6, Inho Yang7, Man Jeong Paik2, Hyukjae Choi4, Hangun Kim2, Sang-Jip Nam5, William Fenical3.
Abstract
Acremonamide (1) was isolated from a marine-derived fungus belonging to the genus Acremonium. The chemical structure of 1 was established using MS, UV, and NMR spectroscopic data analyses. Acremonamide (1) was found to contain N-Me-Phe, N-Me-Ala, Val, Phe, and 2-hydroxyisovaleric acid. The absolute configurations of the four aforementioned amino acids were determined through acid hydrolysis followed by the advanced Marfey's method, whereas the absolute configuration of 2-hydroxyisovaleric acid was determined through GC-MS analysis after formation of the O-pentafluoropropionylated derivative of the (-)-menthyl ester of 2-hydroxyisovaleric acid. As an intrinsic biological activity, acremonamide (1) did not exert cytotoxicity to cancer and noncancer cells and increased the migration and invasion. Based on these activities, the wound healing properties of acremonamide (1) were confirmed in vitro and in vivo.Entities:
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Year: 2021 PMID: 34387477 DOI: 10.1021/acs.jnatprod.1c00305
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050