RATIONAL DESIGN OF POTENT NONPEPTIDAL HIV PROTEASE INHIBITORS

被引：0
|
作者：
GHOSH, AK
CHEN, Y
XU, YB
CHO, WH
BUTHOD, J
HOLLAND, LE
WALTERS, DE
机构：
[1] UNIV ILLINOIS,CHICAGO,IL 60680
[2] IIT,RES INST,DEPT LIFE SCI,CHICAGO,IL 60616
[3] FINCH UNIV HLTH SCI,CHICAGO MED SCH,DEPT BIOL CHEM,N CHICAGO,IL
来源：
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 1995年 / 210卷
关键词：
D O I：
暂无
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
引用
收藏
页码：27 / MEDI
相关论文
共 50 条
  • [1] DENOVO DESIGN AND DISCOVERY OF POTENT, NONPEPTIDAL HIV-1 PROTEASE INHIBITORS
    LAM, PYS
    EYERMANN, CJ
    HODGE, CN
    JADHAV, PK
    RU, Y
    BACHELER, LT
    MEEK, JL
    OTTO, MJ
    RAYNER, MM
    WONG, NY
    CHANG, CH
    WEBER, PC
    JACKSON, DA
    SHARPE, TR
    ERICKSONVIITANEN, SK
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1993, 205 : 96 - MEDI
  • [2] RATIONAL DESIGN OF POTENT, BIOAVAILABLE, NONPEPTIDE CYCLIC UREAS AS HIV PROTEASE INHIBITORS
    LAM, PYS
    JADHAV, PK
    EYERMANN, CJ
    HODGE, CN
    RU, Y
    BACHELER, LT
    MEEK, JL
    OTTO, MJ
    RAYNER, MM
    WONG, YN
    CHANG, CH
    WEBER, PC
    JACKSON, DA
    SHARPE, TR
    ERICKSONVIITANEN, S
    SCIENCE, 1994, 263 (5145) : 380 - 384
  • [3] RATIONAL DESIGN OF POTENT, BIOAVAILABLE NONPEPTIDE CYCLIC UREAS AS HIV PROTEASE INHIBITORS
    ERICKSONVIITANEN, S
    LAM, PYS
    JADHAV, PK
    EYERMANN, CJ
    HODGE, CN
    RU, Y
    BACHELER, LT
    MEEK, JL
    OTTO, MJ
    RAYNER, MM
    WONG, YN
    CHANG, CH
    WEBER, PC
    JACKSON, DA
    SHARPE, TR
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1994, : 167 - 167
  • [4] RATIONAL DRUG DESIGN - INHIBITORS OF RENIN AND HIV PROTEASE
    TURNER, SR
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1992, 204 : 126 - ORGN
  • [5] SYNTHESIS, STRUCTURE-ACTIVITY RELATIONSHIP AND X-RAY STUDIES OF POTENT NONPEPTIDAL CYCLIC HIV PROTEASE INHIBITORS
    RU, Y
    LAM, PYS
    HODGE, CN
    JADHAV, PK
    ALDRICH, PE
    EYERMANN, CJ
    RAYNER, MM
    MEEK, JL
    OTTO, MJ
    CHANG, CH
    WEBER, PC
    ERICKSONVIITANEN, S
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1994, 208 : 36 - MEDI
  • [6] Structure based design:: Novel spirocyclic ethers as nonpeptidal P2-ligands for HIV protease inhibitors
    Ghosh, AK
    Krishnan, K
    Walters, DE
    Cho, WH
    Cho, H
    Koo, Y
    Trevino, J
    Holland, L
    Buthod, J
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1998, 8 (08) : 979 - 982
  • [7] Oximinoarylsulfonamides as potent HIV protease inhibitors
    Yeung, CM
    Klein, LL
    Flentge, CA
    Randolph, JT
    Zhao, C
    Sun, MH
    Dekhtyar, T
    Stoll, VS
    Kempf, DJ
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2005, 15 (09) : 2275 - 2278
  • [8] COMPUTER-ASSISTED DESIGN OF POTENT NONPEPTIDE INHIBITORS OF HIV PROTEASE
    JADHAV, PK
    LAM, PY
    EYERMANN, CJ
    HODGE, CN
    WOERNER, FJ
    BACHELER, LT
    MEEK, UL
    OTTO, MJ
    RAYNER, MM
    WONG, NY
    CHANG, CH
    WEBER, PC
    JACKSON, DA
    SHARPE, TR
    ERICKSONVIITANEN, S
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1993, 205 : 107 - MEDI
  • [9] Nonpeptidal P-2 ligands for HIV protease inhibitors: Structure-based design, synthesis, and biological evaluation
    Ghosh, AK
    Kincaid, JF
    Walters, DE
    Chen, Y
    Chaudhuri, NC
    Thompson, WJ
    Culberson, C
    Fitzgerald, PMD
    Lee, HY
    McKee, SP
    Munson, PM
    Duong, TT
    Darke, PL
    Zugay, JA
    Schleif, WA
    Axel, MG
    Lin, J
    Huff, JR
    JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (17) : 3278 - 3290
  • [10] Rational Design of Antibody Protease Inhibitors
    Liu, Tao
    Fu, Guangsen
    Luo, Xiaozhou
    Liu, Yan
    Wang, Ying
    Wang, Rongsheng E.
    Schultz, Peter G.
    Wang, Feng
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (12) : 4042 - 4045
12345