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Bioorg Med Chem ; 12(15): 4267-73, 2004 Aug 01.
Article in English | MEDLINE | ID: mdl-15246103

ABSTRACT

A series of novel podophyllotoxin derivatives containing structural modifications at C-4 (7-14), C-4' (16-17), and the methylenedioxy A-ring (23-28) was synthesized and tested for inhibition of HIV replication. Four of these compounds (25-28) were previously reported to show EC(50) values of <0.001 microg/mL and therapeutic index (TI) values >120. Three of the newly tested compounds (8, 12, and 20) showed good activity with EC(50) values of 0.012, <0.001, and 0.389 microg/mL and TI values of 19.1, >16, and 19.4, respectively. A comparison of the anti-HIV activity of these derivatives suggested that an opened A-ring with 6,7-dimethoxy substitution and a 4'-demethylated E ring enhanced anti-HIV activity.


Subject(s)
Acquired Immunodeficiency Syndrome , Anti-HIV Agents/pharmacology , HIV-1/drug effects , Virus Replication/drug effects , Anti-HIV Agents/chemical synthesis , Anti-HIV Agents/chemistry , Cell Line , Drug Evaluation, Preclinical , HIV-1/physiology , Humans , Molecular Conformation , Structure-Activity Relationship
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