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Results: 1-13 |
Results: 13
UP-REGULATION OF HIV-1 REPLICATION IN CHRONICALLY INFECTED-CELLS BY INGENOL DERIVATIVES
Authors: FUJIWARA M OKAMOTO M IJICHI K TOKUHISA K HANASAKI Y KATSUURA K UEMURA D SHIGETA S KONNO K YOKOTA T BABA M
Citation: M. Fujiwara et al., UP-REGULATION OF HIV-1 REPLICATION IN CHRONICALLY INFECTED-CELLS BY INGENOL DERIVATIVES, Archives of virology, 143(10), 1998, pp. 2003-2010
RD6-2198, A NOVEL BETAIN-TYPE FLUOROALKYLATED OLIGOMER, INHIBITS THE REPLICATIONS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 AND OTHER ENVELOPED VIRUSES
Authors: FUJIWARA M ASHIDA N OKAMOTO M MIZUTA T IDE T HANASAKI Y KATSUURA K SAWADA H SHIGETA S KONNO K YOKOTA T BABA M
Citation: M. Fujiwara et al., RD6-2198, A NOVEL BETAIN-TYPE FLUOROALKYLATED OLIGOMER, INHIBITS THE REPLICATIONS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 AND OTHER ENVELOPED VIRUSES, Antiviral research, 38(2), 1998, pp. 141-149
INHIBITION OF INTERLEUKIN-6-INDUCED HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 EXPRESSION BY ANTI-GP130 MONOCLONAL-ANTIBODY
Authors: OKAMOTO M YASUKAWA K KATSUURA K BABA M
Citation: M. Okamoto et al., INHIBITION OF INTERLEUKIN-6-INDUCED HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 EXPRESSION BY ANTI-GP130 MONOCLONAL-ANTIBODY, Biochemistry and molecular biology international, 43(4), 1997, pp. 733-740
DISCOVERY OF ANTIINFLUENZA-A VIRUS ACTIVITY OF A CORYNANTHE-TYPE INDOLE ALKALOID, HIRSUTINE, IN-VITRO AND THE STRUCTURE-ACTIVITY RELATIONSHIP OF NATURAL AND SYNTHETIC ANALOGS
Authors: TAKAYAMA H IIMURA Y KITAJIMA M AIMI N KONNO K INOUE H FUJIWARA M MIZUTA T YOKOTA T SHIGETA S TOKUHISA K HANASAKI Y KATSUURA K
Citation: H. Takayama et al., DISCOVERY OF ANTIINFLUENZA-A VIRUS ACTIVITY OF A CORYNANTHE-TYPE INDOLE ALKALOID, HIRSUTINE, IN-VITRO AND THE STRUCTURE-ACTIVITY RELATIONSHIP OF NATURAL AND SYNTHETIC ANALOGS, Bioorganic & medicinal chemistry letters, 7(24), 1997, pp. 3145-3148
HAS THE SUBSTRUCTURE OF QUARKS AND LEPTONS BEEN FOUND ALSO BY THE H1 AND ZEUS DETECTORS AT DESY HERA
Authors: AKAMA K KATSUURA K TERAZAWA H
Citation: K. Akama et al., HAS THE SUBSTRUCTURE OF QUARKS AND LEPTONS BEEN FOUND ALSO BY THE H1 AND ZEUS DETECTORS AT DESY HERA, Physical review. D. Particles and fields, 56(5), 1997, pp. 2490-2494
THIADIAZOLE DERIVATIVES - HIGHLY POTENT AND SELECTIVE INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) REPLICATIONS IN-VITRO
Authors: FUJIWARA M IJICHI K HANASAKI Y IDE T KATSUURA K TAKAYAMA H AIMI N SHIGETA S KONNO K YOKOTA T BABA M
Citation: M. Fujiwara et al., THIADIAZOLE DERIVATIVES - HIGHLY POTENT AND SELECTIVE INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) REPLICATIONS IN-VITRO, Microbiology and immunology, 41(4), 1997, pp. 301-308
INHIBITION OF CHOLESTEROL-BIOSYNTHESIS BY SQUALENE EPOXIDASE INHIBITOR AVOIDS APOPTOTIC CELL-DEATH IN L6 MYOBLASTS
Authors: MATZNO S YAMAUCHI T GOHDA M ISHIDA N KATSUURA K HANASAKI Y TOKUNAGA T ITOH H NAKAMURA N
Citation: S. Matzno et al., INHIBITION OF CHOLESTEROL-BIOSYNTHESIS BY SQUALENE EPOXIDASE INHIBITOR AVOIDS APOPTOTIC CELL-DEATH IN L6 MYOBLASTS, Journal of lipid research, 38(8), 1997, pp. 1639-1648
UTILIZATION OF WIELAND FUROXAN SYNTHESIS FOR PREPARATION OF 4-ARYL-1,2,5-OXADIAZOLE-3-YL CARBAMATE DERIVATIVES HAVING POTENT ANTI-HIV ACTIVITY
Authors: TAKAYAMA H SHIRAKAWA S KITAJIMA M AIMI N YAMAGUCHI K HANASAKI Y IDE T KATSUURA K FUJIWARA M IJICHI K KONNO K SIGETA S YOKOTA T BABA M
Citation: H. Takayama et al., UTILIZATION OF WIELAND FUROXAN SYNTHESIS FOR PREPARATION OF 4-ARYL-1,2,5-OXADIAZOLE-3-YL CARBAMATE DERIVATIVES HAVING POTENT ANTI-HIV ACTIVITY, Bioorganic & medicinal chemistry letters, 6(16), 1996, pp. 1993-1996
INGENOL DERIVATIVES ARE HIGHLY POTENT AND SELECTIVE INHIBITORS OF HIVREPLICATION IN-VITRO
Authors: FUJIWARA M IJICHI K TOKUHISA K KATSUURA K WANG GYS UEMURA D SHIGETA S KONNO K YOKOTA T BABA M
Citation: M. Fujiwara et al., INGENOL DERIVATIVES ARE HIGHLY POTENT AND SELECTIVE INHIBITORS OF HIVREPLICATION IN-VITRO, Antiviral chemistry & chemotherapy, 7(5), 1996, pp. 230-236
ANTI-HIV-1 ACTIVITY OF THIADIAZOLE DERIVATIVES - STRUCTURE-ACTIVITY RELATIONSHIP, REVERSE-TRANSCRIPTASE INHIBITION, AND LIPOPHILICITY
Authors: IJICHI K FUJIWARA M NAGANO H MATSUMOTO Y HANASAKI Y IDE T KATSUURA K TAKAYAMA H SHIRAKAWA S AIMI N SHIGETA S KONNO K MATSUSHIMA M YOKOTA T BABA M
Citation: K. Ijichi et al., ANTI-HIV-1 ACTIVITY OF THIADIAZOLE DERIVATIVES - STRUCTURE-ACTIVITY RELATIONSHIP, REVERSE-TRANSCRIPTASE INHIBITION, AND LIPOPHILICITY, Antiviral research, 31(1-2), 1996, pp. 87-94
MECHANISM OF SELECTIVE-INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS BY INGENOL TRIACETATE
Authors: FUJIWARA M IJICHI K TOKUHISA K KATSUURA K SHIGETA S KONNO K WANG GYS UEMURA D YOKOTA T BABA M
Citation: M. Fujiwara et al., MECHANISM OF SELECTIVE-INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS BY INGENOL TRIACETATE, Antimicrobial agents and chemotherapy, 40(1), 1996, pp. 271-273
POTENT AND SPECIFIC-INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1REPLICATION BY 4-(2,6-DICHLOROPHENYL)-1,2,5-THIADIAZOL-3-YL N,N-DIALKYLCARBAMATE DERIVATIVES
Authors: IJICHI K FUJIWARA M HANASAKI Y WATANABE H KATSUURA K TAKAYAMA H SHIRAKAWA S SAKAI S SHIGETA S KONNO K YOKOTA T BABA M
Citation: K. Ijichi et al., POTENT AND SPECIFIC-INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1REPLICATION BY 4-(2,6-DICHLOROPHENYL)-1,2,5-THIADIAZOL-3-YL N,N-DIALKYLCARBAMATE DERIVATIVES, Antimicrobial agents and chemotherapy, 39(10), 1995, pp. 2337-2340
THIADIAZOLE DERIVATIVES - HIGHLY POTENT AND SPECIFIC HIV-1 REVERSE-TRANSCRIPTASE INHIBITORS
Authors: HANASAKI Y WATANABE H KATSUURA K TAKAYAMA H SHIRAKAWA S YAMAGUCHI K SAKAI S IJICHI K FUJIWARA M KONNO K YOKOTA T SHIGETA S BABA M
Citation: Y. Hanasaki et al., THIADIAZOLE DERIVATIVES - HIGHLY POTENT AND SPECIFIC HIV-1 REVERSE-TRANSCRIPTASE INHIBITORS, Journal of medicinal chemistry, 38(12), 1995, pp. 2038-2040
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