STRUCTURE-BASED DESIGN OF HIV-1 PROTEASE INHIBITORS - REPLACEMENT OF 2 AMIDES AND A 10-PI-AROMATIC SYSTEM BY A FUSED BIS-TETRAHYDROFURAN

被引:63
作者
GHOSH, AK
THOMPSON, WJ
FITZGERALD, PMD
CULBERSON, JC
AXEL, MG
MCKEE, SP
HUFF, JR
ANDERSON, PS
机构
[1] MERCK SHARP & DOHME LTD,RES LABS,DEPT MED CHEM,W POINT,PA 19486
[2] MERCK SHARP & DOHME LTD,RES LABS,DEPT BIOPHYS CHEM,W POINT,PA 19486
[3] MERCK SHARP & DOHME LTD,RES LABS,DEPT MOLEC SYST,W POINT,PA 19486
关键词
D O I
10.1021/jm00042a002
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
[No abstract available]
引用
收藏
页码:2506 / 2508
页数:3
相关论文
共 13 条
  • [1] COREY EJ, 1993, TETRAHEDRON LETT, V32, P4623
  • [2] ANTIVIRAL PROPERTIES OF RO 31-8959, AN INHIBITOR OF HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) PROTEINASE
    CRAIG, JC
    DUNCAN, IB
    HOCKLEY, D
    GRIEF, C
    ROBERTS, NA
    MILLS, JS
    [J]. ANTIVIRAL RESEARCH, 1991, 16 (04) : 295 - 305
  • [3] N,N'-DISUCCINIMIDYL CARBONATE - A USEFUL REAGENT FOR ALKOXYCARBONYLATION OF AMINES
    GHOSH, AK
    DUONG, TT
    MCKEE, SP
    THOMPSON, WJ
    [J]. TETRAHEDRON LETTERS, 1992, 33 (20) : 2781 - 2784
  • [4] POTENT HIV PROTEASE INHIBITORS - THE DEVELOPMENT OF TETRAHYDROFURANYLGLYCINES AS NOVEL P(2)-LIGANDS AND PYRAZINE AMIDES AS P(3)-LIGANDS
    GHOSH, AK
    THOMPSON, WJ
    HOLLOWAY, MK
    MCKEE, SP
    DUONG, TT
    LEE, HY
    MUNSON, PM
    SMITH, AM
    WAI, JM
    DARKE, PL
    ZUGAY, JA
    EMINI, EA
    SCHLEIF, WA
    HUFF, JR
    ANDERSON, PS
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1993, 36 (16) : 2300 - 2310
  • [5] DI(2-PYRIDYL) CARBONATE PROMOTED ALKOXYCARBONYLATION OF AMINES - A CONVENIENT SYNTHESIS OF FUNCTIONALIZED CARBAMATES
    GHOSH, AK
    DUONG, TT
    MCKEE, SP
    [J]. TETRAHEDRON LETTERS, 1991, 32 (34) : 4251 - 4254
  • [6] 3-TETRAHYDROFURAN AND PYRAN URETHANES AS HIGH-AFFINITY P2-LIGANDS FOR HIV-1 PROTEASE INHIBITORS
    GHOSH, AK
    THOMPSON, WJ
    MCKEE, SP
    DUONG, TT
    LYLE, TA
    CHEN, JC
    DARKE, PL
    ZUGAY, JA
    EMINI, EA
    SCHLEIF, WA
    HUFF, JR
    ANDERSON, PS
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1993, 36 (02) : 292 - 294
  • [7] AFFINITY PURIFICATION OF THE HIV-1 PROTEASE
    HEIMBACH, JC
    GARSKY, VM
    MICHELSON, SR
    DIXON, RAF
    SIGAL, IS
    DARKE, PL
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 164 (03) : 955 - 960
  • [8] NOVEL BINDING MODE OF HIGHLY POTENT HIV-PROTEINASE INHIBITORS INCORPORATING THE (R)-HYDROXYETHYLAMINE ISOSTERE
    KROHN, A
    REDSHAW, S
    RITCHIE, JC
    GRAVES, BJ
    HATADA, MH
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1991, 34 (11) : 3340 - 3342
  • [9] RECENT ADVANCES IN THE DESIGN OF HIV PROTEINASE-INHIBITORS
    MARTIN, JA
    [J]. ANTIVIRAL RESEARCH, 1992, 17 (04) : 265 - 278
  • [10] RATIONAL DESIGN OF PEPTIDE-BASED HIV PROTEINASE-INHIBITORS
    ROBERTS, NA
    MARTIN, JA
    KINCHINGTON, D
    BROADHURST, AV
    CRAIG, JC
    DUNCAN, IB
    GALPIN, SA
    HANDA, BK
    KAY, J
    KROHN, A
    LAMBERT, RW
    MERRETT, JH
    MILLS, JS
    PARKES, KEB
    REDSHAW, S
    RITCHIE, AJ
    TAYLOR, DL
    THOMAS, GJ
    MACHIN, PJ
    [J]. SCIENCE, 1990, 248 (4953) : 358 - 361