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Volumn 11, Issue 15, 2001, Pages 1993-1995
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Synthesis of N-alkyl substituted indolocarbazoles as potent inhibitors of human cytomegalovirus replication
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Author keywords
[No Author keywords available]
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Indexed keywords
12 ETHYL 12,13 DIHYDRO 5H INDOLO[3,4 C]CARBAZOLE 5,7(6H) DIONE;
ALKYL GROUP;
ANTIVIRUS AGENT;
ARCYRIAFLAVIN A;
GANCICLOVIR;
INDOLE DERIVATIVE;
INDOLECARBAZOLE DERIVATIVE;
NITROGEN;
UNCLASSIFIED DRUG;
ALKYLATION;
ANIMAL CELL;
ANTIBIOTIC RESISTANCE;
ARTICLE;
CELL CULTURE;
CONTROLLED STUDY;
CYTOMEGALOVIRUS;
DRUG MECHANISM;
DRUG POTENCY;
DRUG SCREENING;
DRUG SYNTHESIS;
HERPES SIMPLEX VIRUS 1;
HERPES SIMPLEX VIRUS 2;
HUMAN IMMUNODEFICIENCY VIRUS 1;
IC 50;
INFLUENZA VIRUS A;
NONHUMAN;
STRUCTURE ACTIVITY RELATION;
VARICELLA ZOSTER VIRUS;
VIRUS INHIBITION;
VIRUS ISOLATION;
VIRUS REPLICATION;
ANTIVIRAL AGENTS;
CARBAZOLES;
CELLS, CULTURED;
CYTOMEGALOVIRUS;
DRUG RESISTANCE;
GANCICLOVIR;
HUMANS;
INDOLES;
INHIBITORY CONCENTRATION 50;
PROTEIN KINASE C;
STRUCTURE-ACTIVITY RELATIONSHIP;
VIRUS REPLICATION;
HUMAN HERPESVIRUS 5;
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EID: 0035817257
PISSN: 0960894X
EISSN: None
Source Type: Journal
DOI: 10.1016/S0960-894X(01)00352-3 Document Type: Article |
Times cited : (30)
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References (24)
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