| Literature DB >> 19921834 |
Usama W Hawas1, Mohamed Shaaban, Khaled A Shaaban, Michael Speitling, Armin Maier, Gerhard Kelter, Heinz H Fiebig, Marinus Meiners, Elisabeth Helmke, Hartmut Laatsch.
Abstract
Chemical screening of the ethyl acetate extract from the marine-derived Streptomyces sp. isolate Mei37 resulted in five isoquinolinequinones, four new derivatives, mansouramycin A-D (1, 3-5), and the known 3-methyl-7-(methylamino)-5,8-isoquinolinedione (2). Their structures were elucidated by NMR and MS techniques and by comparison with related compounds. Cytotoxicity profiling of the mansouramycins in a panel of up to 36 tumor cell lines indicated significant cytotoxicity of several derivatives, with pronounced selectivity for non-small cell lung cancer, breast cancer, melanoma, and prostate cancer cells.Entities:
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Year: 2009 PMID: 19921834 DOI: 10.1021/np900160g
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050