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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/21144
Title: Isolation and structure elucidation of enniatins L, M<inf>1</inf>, M<inf>2</inf>, and N: Novel hydroxy analogs
Authors: Pornrapee Vongvilai
Masahiko Isaka
Prasat Kittakoop
Prasert Srikitikulchai
Palangpon Kongsaeree
Samran Prabpai
Yodhathai Thebtaranonth
Mahidol University
Thailand National Center for Genetic Engineering and Biotechnology
Keywords: Biochemistry, Genetics and Molecular Biology;Chemical Engineering;Chemistry;Pharmacology, Toxicology and Pharmaceutics
Issue Date: 4-Oct-2004
Citation: Helvetica Chimica Acta. Vol.87, No.8 (2004), 2066-2073
Abstract: Four new cyclohexadepsipeptides, enniatins L (1), M1(2), M2(3), and N (4), have been isolated from an unidentified fungus (BCC 2629), together with the known enniatins B (5), H (6), and I (7), MK1688 (8), and enniatin B4(9). Compounds 1-4 are the first enniatin analogs with an OH group at the side chain of one of the 2-hydroxycarboxylic acid residues. The structures of 1-4 were elucidated by spectroscopic means and by X-ray crystallography.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=4644288194&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/21144
ISSN: 0018019X
Appears in Collections:Scopus 2001-2005

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