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Novel non-nucleoside inhibitors of HIV-1 reverse transcriptase. III: Dipyrido[2,3-b:2',3'-e]diazepinonesPROUDFOOT, J. R; PATEL, U. R; KAPADIA, S. R et al.Journal of medicinal chemistry (Print). 1995, Vol 38, Num 8, pp 1406-1410, issn 0022-2623Article

In vitro protein-binding characteristics of atevirdine and its N-dealkylated metaboliteROSSER, L. M; O'DONNELL, A. M; LEE, K. M et al.Antiviral research. 1994, Vol 25, Num 3-4, pp 193-200, issn 0166-3542Article

Use of viral resistance patterns to antiretroviral drugs in optimising selection of drug combinations and sequencesMOYLE, G. J.Drugs (Basel). 1996, Vol 52, Num 2, pp 168-185, issn 0012-6667Article

Characterization of the antiviral activity of highly substituted pyrroles : a novel class of non-nucleoside HIV-1 reverse transcriptase inhibitorANTONUCCI, T; WARMUS, J. S; HODGES, J. C et al.Antiviral chemistry & chemotherapy. 1995, Vol 6, Num 2, pp 98-108, issn 0956-3202Article

Effects of a non-xanthine adenosine antagonist, CGS 15943, and a phosphodiesterase inhibitor, Ro 20-1724, in a light/dark test in miceIMAIZUMI, M; MIYAZAKI, S; ONODERA, K et al.Methods and findings in experimental and clinical pharmacology. 1994, Vol 16, Num 10, pp 717-721, issn 0379-0355Article

Isolation and characterization of human immunodeficiency virus type-1 mutants resistant to the non-nucleotide reverse transcriptase inhibitor MKC-442SEKI, M; SADAKATA, Y; YUASA, S et al.Antiviral chemistry & chemotherapy. 1995, Vol 6, Num 2, pp 73-79, issn 0956-3202Article

Oxathiin carboxanilide derivatives: a class of non-nucleoside HIV-1-specific reverse transcriptase inhibitors (NNRTIs) that are active against mutant HIV-1 strains resistant to other NNRTIsBALZARINI, J; JONCKHEERE, H; HARRISON, W. A et al.Antiviral chemistry & chemotherapy. 1995, Vol 6, Num 3, pp 169-178, issn 0956-3202Article

Synthesis and anti-HIV activity of [AZT]-[TSAO-T] and [AZT]-[HEPT] dimers as potential multifunctional inhibitors of HIV-1 reverse transcriptaseVELAZQUEZ, S; ALVAREZ, R; SAN-FELIX, A et al.Journal of medicinal chemistry (Print). 1995, Vol 38, Num 10, pp 1641-1649, issn 0022-2623Article

Inhibition of human immunodeficiency virus type 1 wild-type and mutant reverse transcriptases by the phenyl ethyl thiazolyl thiourea derivatives trovirdine and MSC-127HONG ZHANG; VRANG, L; BÄCKBRO, K et al.Antiviral research. 1995, Vol 28, Num 4, pp 331-342, issn 0166-3542Article

All-atom models for the non-nucleoside binding site of HIV-1 reverse transcriptase complexed with inhibitors : A 3D QSAR approachGUSSIO, R; NAGARAJAN PATTABIRAMAN; ZAHAREVITZ, D. W et al.Journal of medicinal chemistry (Print). 1996, Vol 39, Num 8, pp 1645-1650, issn 0022-2623Article

Synthesis and anti-HIV-1 activity of thio analogues of dihydroalkoxybenzyloxopyrimidinesMAI, A; ARTICO, M; SBARDELLA, G et al.Journal of medicinal chemistry (Print). 1995, Vol 38, Num 17, pp 3258-3263, issn 0022-2623Article

Indoles and pyridazino[4,5-b]indoles as nonnucleaside analog inhibitors of HIV-1 reverse transcriptaseFONT, M; MONGE, A; BORRAS, F et al.European journal of medicinal chemistry. 1995, Vol 30, Num 12, pp 963-971, issn 0223-5234Article

Knocking out human immunodeficiency virus through non-nucleoside reverse transcriptase inhibitors used as single agents or in combinations : a paradigm for the cure of AIDS ?DE CLERCQ, E; BALZARINI, J.Il Farmaco (Pavia). 1995, Vol 50, Num 11, pp 735-747, issn 0014-827XConference Paper

Complexes of HIV-1 reverse transcriptase with inhibitors of the HEPT series reveal conformational changes relevant to the design of potent non-nucleoside inhibitorsHOPKINS, A. L; JINGSHAN REN; STUART, D. I et al.Journal of medicinal chemistry (Print). 1996, Vol 39, Num 8, pp 1589-1600, issn 0022-2623Article

New arylpyrido-diazepine and -thiodiazepine derivatives are potent and highly selective HIV-1 inhibitors targeted at the reverse transcriptaseBELLAROSA, D; ANTONELLI, G; DESMYTER, J et al.Antiviral research. 1996, Vol 30, Num 2-3, pp 109-124, issn 0166-3542Article

Molecular modeling and quantitative structure-activity studies of anti-HIV-1 2-heteroarylquinoline-4-aminesKIREEV, D. B; CHRETIEN, J. R; RAEVSKY, O. A et al.European journal of medicinal chemistry. 1995, Vol 30, Num 5, pp 395-402, issn 0223-5234Article

Etude Synthétique de Dérivés Isoxazolo[3,4-e]pyrimido[1,2-a][1,3]diazocine ou [1,3]diazépine. Potentiellement Inhibiteurs de la Transcriptase Inverse du VIH 1 = Synthetic studies of isoxazolo[3,4-e]pyrimido[1,2-a][1,3]diazocine or [1,3]diazepine derivatives as potential Non Nucleoside Reverse Transcriptase InhibitorsPerez, Caroline; Grierson, D.-S.1995, 234 p.Thesis

Synthesis and antiviral evaluation of fluorinated dipyridodiazepinones and dipyridodiazepines (nevirapine derivatives)BOYODE, B. P; SINET, M; FARESSE, A et al.Antiviral chemistry & chemotherapy. 1995, Vol 6, Num 3, pp 162-168, issn 0956-3202Article

A new series of pyridinone derivatives as potent non-nucleoside human immunodeficiency virus type 1 specific reverse transcriptase inhibitorsDOLLE, V; FAN, E; CHI HUNG NGUYEN et al.Journal of medicinal chemistry (Print). 1995, Vol 38, Num 23, pp 4679-4686, issn 0022-2623Article

Novel non-nucleoside inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase. IV: 2-substituted dipyridodiazepinones as potent inhibitors of both wild-type and cysteine-181 HIV-1 reverse transcriptase enzymesPROUDFOOT, J. R; HARGRAVE, K. D; ROSE, J et al.Journal of medicinal chemistry (Print). 1995, Vol 38, Num 24, pp 4830-4838, issn 0022-2623Article

Novel non-nucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase. V: 4-Substituted and 2,4-disubstituted analogs of nevirapineKELLY, T. A; PROUDFOOT, J. R; MCNEIL, D. W et al.Journal of medicinal chemistry (Print). 1995, Vol 38, Num 24, pp 4839-4847, issn 0022-2623Article

Phenethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. I: Synthesis and basic structure-activity relationship studies of PETT analogsBELL, F. W; CANTRELL, A. S; ÖBERG, B et al.Journal of medicinal chemistry (Print). 1995, Vol 38, Num 25, pp 4929-4936, issn 0022-2623Article

Synthesis of non-nucleoside analogs of toyocamycin, sangivamycin, and thiosangivamycin : influence of various 7-substituents on antiviral activityRENAU, T. E; WOTRING, L. L; DRACH, J. C et al.Journal of medicinal chemistry (Print). 1995, Vol 39, Num 4, pp 873-880, issn 0022-2623Article

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