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Abstract
The title complexes I (R = CH2Ph, CHMe2, CH2CHMe2, CHMeEt, (CH2)2SMe) were prepd. from substituted L-1,2-diaminoethanes derived from L-alpha -amino acids and tested for antitumor activity in vitro. I inhibited DNA formation in hormone independent human mammary carcinoma cell line MDA-MB 231.
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