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Antimicrobial Agents and Chemotherapy|October 1, 1986
Mode of action, toxicity, pharmacokinetics, and efficacy of some new antiherpesvirus guanosine analogs related to buciclovirA Larsson, K Stenberg, A C Ericson, et al.Biochemical Pharmacology|January 1, 1989
An analysis of the inhibition of replication of HIV and MuLV by some 3'-blocked pyrimidine analogsH Bazin, J Chattopadhyaya, R Datema, et al.Bioorganic & Medicinal Chemistry|June 18, 1998
Synthesis and antiviral activity of prodrugs of the nucleoside 1-[2',3'-dideoxy-3'-C-(hydroxymethyl)-beta-D-erythropentofuranosyl] cytosineS C Mauldin, C J Paget, C D Jones, et al.Antimicrobial Agents and Chemotherapy|June 1, 1977
Inhibition of influenza virus ribonucleic acid polymerase by ribavirin triphosphateB Eriksson, E Helgstrand, N G Johansson, et al.Science (New York, N.Y.)|September 1, 1978
Trisodium phosphonoformate, a new antiviral compoundE Helgstrand, B Eriksson, N G Johansson, et al.Journal of Medicinal Chemistry|December 8, 1995
Phenethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis and basic structure-activity relationship studies of PETT analogsF W Bell, A S Cantrell, M Högberg, et al.Journal of Medicinal Chemistry|October 9, 1999
Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analoguesM Högberg, C Sahlberg, P Engelhardt, et al.Journal of Medicinal Chemistry|October 11, 1996
Phenethylthiazolylthiourea (PETT) compounds as a new class of HIV-1 reverse transcriptase inhibitors. 2. Synthesis and further structure-activity relationship studies of PETT analogsA S Cantrell, P Engelhardt, M Högberg, et al.Pageof 3