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J Med Chem ; 44(22): 3754-7, 2001 Oct 25.
Article in English | MEDLINE | ID: mdl-11606141

ABSTRACT

A new 7,8-methylenedioxy analogue (4) of (+)-porothramycin B (2) and its water-soluble sodium bisulfite derivative (15) have been synthesized in high yields and have been shown to exhibit high cytotoxic activities against several tumor cell lines. The new pyrrolo[2,1-c][1,4]benzodiazepine 4 was as effective against the resistant cell lines as against the doxorubicin-sensitive cell lines tested.


Subject(s)
Anthramycin/chemical synthesis , Antineoplastic Agents/chemical synthesis , Doxorubicin/pharmacology , Anthramycin/analogs & derivatives , Anthramycin/chemistry , Anthramycin/pharmacology , Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Drug Resistance, Neoplasm , Drug Screening Assays, Antitumor , Humans , Stereoisomerism , Structure-Activity Relationship , Tumor Cells, Cultured
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