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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/22988
Title: Cyclopentenones, scaffolds for organic syntheses produced by the endophytic fungus mitosporic dothideomycete sp. LRUB20
Authors: Porntep Chomcheon
Nongluksna Sriubolmas
Suthep Wiyakrutta
Nattaya Ngamrojanavanich
Narongsak Chaichit
Chulabhorn Mahidol
Somsak Ruchirawat
Prasat Kittakoop
Chulalongkorn University
Mahidol University
Thammasat University
Chulabhorn Research Institute
Keywords: Biochemistry, Genetics and Molecular Biology;Chemistry;Medicine;Pharmacology, Toxicology and Pharmaceutics
Issue Date: 1-Sep-2006
Citation: Journal of Natural Products. Vol.69, No.9 (2006), 1351-1353
Abstract: Two new natural products, 2-hydroxymethyl-3-methylcyclopent-2-enone (1) (synthetically known) and cis-2-hydroxymethyl-3-methylcyclopentanone (2), and a known compound, asterric acid (3), were isolated from the endophytic fungus mitosporic Dothideomycete sp. LRUB20, which was isolated from the stem of the Thai medicinal plant Leea rubra. Compound 2 was separated and identified in the form of its 2,4-dinitrophenylhydrazone derivative (5). Compounds 1, 3, and hydrazone 5 exhibited mild antimycobacterial activity, both with MIC values of 200 μg/mL. Compounds 1, 3, and 4 were inactive (at 50 μg/mL) toward Vero, KB, NCI-H187, and BC cell lines. Hydrazone 5 showed only mild cytotoxicity against the Vero cell line with an IC50 value of 21.7 μg/mL; however, it was inactive toward KB, NCI-H187, and BC cell lines. Endophytic fungi may be a source for the production of building blocks for organic syntheses. © 2006 American Chemical Society and American Society of Pharmacognosy.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33750033691&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/22988
ISSN: 01633864
Appears in Collections:Scopus 2006-2010

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