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Results: 1-8 |
Results: 8
SOME ASPECTS ON ACYCLONUCLEOSIDE SYNTHESIS
Authors: UBASAWA M TAKASHIMA H SEKIYA K
Citation: M. Ubasawa et al., SOME ASPECTS ON ACYCLONUCLEOSIDE SYNTHESIS, Nucleosides & nucleotides, 17(12), 1998, pp. 2241-2247
MOLECULAR SIMULATION OF 5,6-SUBSTITUTED 1-[(2-HYDROXYETHOXY)METHYL]URACILS WITH ANTI-HIV-1 ACTIVITY
Authors: MAGER PP DECLERCQ E TAKASHIMA H UBASAWA M SEKIYA K BABA M WALTHER H
Citation: Pp. Mager et al., MOLECULAR SIMULATION OF 5,6-SUBSTITUTED 1-[(2-HYDROXYETHOXY)METHYL]URACILS WITH ANTI-HIV-1 ACTIVITY, European journal of medicinal chemistry, 31(9), 1996, pp. 701-712
HEPT DERIVATIVES - 6-BENZYL-1-ETHOXYMETHYL-5-ISOPROPYLURACIL (MKC-442)
Authors: BABA M TANAKA H MIYASAKA T YUASA S UBASAWA M WALKER RT DECLERCQ E
Citation: M. Baba et al., HEPT DERIVATIVES - 6-BENZYL-1-ETHOXYMETHYL-5-ISOPROPYLURACIL (MKC-442), Nucleosides & nucleotides, 14(3-5), 1995, pp. 575-583
SYNTHESIS AND ANTIVIRAL ACTIVITY OF 6-BENZYL ANALOGS OF 1-[(2-HYDROXYETHOXY)METHYL]-6-(PHENYLTHIO)THYMINE (HEPT) AS POTENT AND SELECTIVE ANTI-HIV-1 AGENTS
Authors: TANAKA H TAKASHIMA H UBASAWA M SEKIYA K INOUYE N BABA M SHIGETA S WALKER RT DECLERCQ E MIYASAKA T
Citation: H. Tanaka et al., SYNTHESIS AND ANTIVIRAL ACTIVITY OF 6-BENZYL ANALOGS OF 1-[(2-HYDROXYETHOXY)METHYL]-6-(PHENYLTHIO)THYMINE (HEPT) AS POTENT AND SELECTIVE ANTI-HIV-1 AGENTS, Journal of medicinal chemistry, 38(15), 1995, pp. 2860-2865
A CONVENIENT ONE-POT SYNTHESIS OF ACYCLONUCLEOSIDES
Authors: UBASAWA M TAKASHIMA H SEKIYA K
Citation: M. Ubasawa et al., A CONVENIENT ONE-POT SYNTHESIS OF ACYCLONUCLEOSIDES, Chemical and Pharmaceutical Bulletin, 43(1), 1995, pp. 142-143
PRECLINICAL EVALUATION OF MKC-442, A HIGHLY POTENT AND SPECIFIC INHIBITOR OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 IN-VITRO
Authors: BABA M SHIGETA S YUASA S TAKASHIMA H SEKIYA K UBASAWA M TANAKA H MIYASAKA T WALKER RT DECLERCQ E
Citation: M. Baba et al., PRECLINICAL EVALUATION OF MKC-442, A HIGHLY POTENT AND SPECIFIC INHIBITOR OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 IN-VITRO, Antimicrobial agents and chemotherapy, 38(4), 1994, pp. 688-692
SELECTIVE AND SYNERGISTIC INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REVERSE-TRANSCRIPTASE BY A NONNUCLEOSIDE INHIBITOR, MKC-442
Authors: YUASA S SADAKATA Y TAKASHIMA H SEKIYA K INOUYE N UBASAWA M BABA M
Citation: S. Yuasa et al., SELECTIVE AND SYNERGISTIC INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REVERSE-TRANSCRIPTASE BY A NONNUCLEOSIDE INHIBITOR, MKC-442, Molecular pharmacology, 44(4), 1993, pp. 895-900
EFFECT OF HUMAN SERUM ON THE IN-VITRO ANTI-HIV-1 ACTIVITY OF 1-[(2-HYDROXYETHOXY)METHYL]-6-(PHENYLTHIO)THYMINE (HEPT) DERIVATIVES AS RELATED TO THEIR LIPOPHILICITY AND SERUM-PROTEIN BINDING
Authors: BABA M YUASA S NIWA T YAMAMOTO M YABUUCHI S TAKASHIMA H UBASAWA M TANAKA H MIYASAKA T WALKER RT BALZARINI J DECLERCQ E SHIGETA S
Citation: M. Baba et al., EFFECT OF HUMAN SERUM ON THE IN-VITRO ANTI-HIV-1 ACTIVITY OF 1-[(2-HYDROXYETHOXY)METHYL]-6-(PHENYLTHIO)THYMINE (HEPT) DERIVATIVES AS RELATED TO THEIR LIPOPHILICITY AND SERUM-PROTEIN BINDING, Biochemical pharmacology, 45(12), 1993, pp. 2507-2512
Risultati: 1-8 |