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Bioorg Med Chem ; 12(1): 103-12, 2004 Jan 02.
Article in English | MEDLINE | ID: mdl-14697775

ABSTRACT

Several heterocycles, such as benzimidazoles, quinoxalines and indoles incorporated into a hydrophenanthrene and naphthalene skeleton, were synthesised from two useful ortho-bromonitro precursors derived from dehydroabietic acid: methyl 12-bromo-13-nitro-deisopropyldehydroabietate and methyl 12-bromo-13,14-dinitro-deisopropyldehydroabietate. The new heterocycles were evaluated for their activity in vitro against several RNA and DNA viruses.


Subject(s)
Abietanes/chemical synthesis , Antiviral Agents/pharmacology , Benzimidazoles/chemical synthesis , Indoles/chemical synthesis , Quinoxalines/chemical synthesis , Abietanes/pharmacology , Animals , Benzimidazoles/pharmacology , Cell Line , Chlorocebus aethiops , Cytomegalovirus/drug effects , Drug Evaluation, Preclinical/methods , Fibroblasts/drug effects , Fibroblasts/virology , HeLa Cells , Herpesvirus 1, Human/drug effects , Herpesvirus 2, Human/drug effects , Herpesvirus 3, Human/drug effects , Humans , Indoles/pharmacology , Quinoxalines/pharmacology , Sindbis Virus/drug effects , Vero Cells
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