L735,524 - THE RATIONAL DESIGN OF A POTENT AND ORALLY BIOAVAILABLE HIV PROTEASE INHIBITOR

被引:0
|
作者
DORSEY, BD
LEVIN, RB
MCDANIEL, SL
VACCA, JP
DARKE, PL
ZUGAY, JA
EMINI, EA
SCHLEIF, WA
QUINTERO, JC
LIN, JH
CHEN, IW
OSTOVIC, D
FITZGERALD, PMD
HOLLOWAY, MK
ANDERSON, PS
HUFF, JR
机构
[1] MERCK SHARP & DOHME LTD,DEPT MED CHEM,W POINT,PA 19486
[2] MERCK SHARP & DOHME LTD,DEPT MOLEC BIOL,W POINT,PA 19486
[3] MERCK SHARP & DOHME LTD,DEPT VIRUS & CELL BIOL,W POINT,PA 19486
[4] MERCK SHARP & DOHME LTD,DEPT DRUG METAB,W POINT,PA 19486
[5] MERCK SHARP & DOHME LTD,DEPT PHARMACEUT RES,W POINT,PA 19486
[6] MERCK SHARP & DOHME LTD,DEPT BIOPHYS CHEM,W POINT,PA 19486
[7] MERCK SHARP & DOHME LTD,DEPT MOLEC SYST,W POINT,PA 19486
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:6 / MEDI
相关论文
共 50 条
  • [21] RATIONAL DESIGN OF POTENT NONPEPTIDAL HIV PROTEASE INHIBITORS
    GHOSH, AK
    CHEN, Y
    XU, YB
    CHO, WH
    BUTHOD, J
    HOLLAND, LE
    WALTERS, DE
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1995, 210 : 27 - MEDI
  • [22] HIGHLY DIASTEREOSELECTIVE REACTION OF A CHIRAL, NON-RACEMIC AMIDE ENOLATE WITH (S)-GLYCIDYL TOSYLATE - SYNTHESIS OF THE ORALLY-ACTIVE HIV-1 PROTEASE INHIBITOR L-735,524
    ASKIN, D
    ENG, KK
    ROSSEN, K
    PURICK, RM
    WELLS, KM
    VOLANTE, RP
    REIDER, PJ
    TETRAHEDRON LETTERS, 1994, 35 (05) : 673 - 676
  • [23] CRYSTAL-STRUCTURE OF HIV-1 PROTEASE IN COMPLEX WITH VX-478, A POTENT AND ORALLY BIOAVAILABLE INHIBITOR OF THE ENZYME
    KIM, EE
    BAKER, CT
    DWYER, MD
    MURCKO, MA
    RAO, BG
    TUNG, RD
    NAVIA, MA
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (03) : 1181 - 1182
  • [24] Orally bioavailable highly potent HIV protease inhibitors against PI-resistant virus
    Lu, ZJ
    Bohn, J
    Rano, T
    Rutkowski, CA
    Simcoe, AL
    Olsen, DB
    Schleif, WA
    Carella, A
    Gabryelski, L
    Jin, LX
    Lin, JH
    Emini, E
    Chapman, K
    Tata, JR
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2005, 15 (23) : 5311 - 5314
  • [25] Structure-based discovery of tipranavir disodium (PNU-140690E): A potent, orally bioavailable, nonpeptidic HIV protease inhibitor
    Thaisrivongs, S
    Strohbach, JW
    BIOPOLYMERS, 1999, 51 (01) : 51 - 58
  • [26] Design, synthesis, and biological evaluation of a potent and orally bioavailable FGFRs inhibitor for fibrotic treatment
    Yue, Lin
    Tan, Zui
    Wei, Wei
    Liu, Hongyao
    Xue, Taixiong
    Su, Xingping
    Wu, Xiuli
    Xie, Yuting
    Li, Peilin
    Wang, Doudou
    Liu, Zhihao
    Gan, Cailing
    Ye, Tinghong
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2025, 285
  • [27] Discovery of a Pyrimidinedione Derivative as a Potent and Orally Bioavailable Axl Inhibitor
    Zhang, Hefeng
    Peng, Xia
    Dai, Yang
    Shao, Jingwei
    Ji, Yinchun
    Sun, Yiming
    Liu, Bo
    Cheng, Xu
    Ai, Jing
    Duan, Wenhu
    JOURNAL OF MEDICINAL CHEMISTRY, 2021, 64 (07) : 3956 - 3975
  • [28] POTENT, ORALLY BIOAVAILABLE HIV-1 PROTEASE INHIBITORS CONTAINING NONCODED D-AMINO ACIDS
    MUNROE, JE
    SHEPHERD, TA
    JUNGHEIM, LN
    HORNBACK, WJ
    HATCH, SD
    MUESING, MA
    WISKERCHEN, MA
    SU, KS
    CAMPANALE, KM
    BAXTER, AJ
    COLACINO, JM
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1995, 5 (23) : 2897 - 2902
  • [29] Discovery of Raltegravir, a potent, selective orally bioavailable HIV-integrase inhibitor for the treatment of HIV-AIDS infection
    Summa, Vincenzo
    Petrocchi, Alessia
    Bonelli, Fabio
    Crescenzi, Benedetta
    Donghi, Monica
    Ferrara, Marco
    Fiore, Fabrizio
    Gardelli, Cristina
    Paz, Odalys Gonzalez
    Hazuda, Daria J.
    Jones, Philip
    Kinzel, Olaf
    Laufer, Ralph
    Monteagudo, Edith
    Muraglia, Ester
    Nizi, Emanuela
    Orvieto, Federica
    Pace, Paola
    Pescatore, Giovanna
    Scarpelli, Rita
    Stillmock, Kara
    Witmer, Marc V.
    Rowley, Michael
    JOURNAL OF MEDICINAL CHEMISTRY, 2008, 51 (18) : 5843 - 5855
  • [30] Design and synthesis of bicyclic pyrimidinones as potent and orally bioavailable HIV-1 integrase inhibitors
    Muraglia, Ester
    Kinzel, Olaf
    Gardelli, Cristina
    Crescenzi, Benedetta
    Donghi, Monica
    Ferrara, Marco
    Nizi, Emanuela
    Orvieto, Federica
    Pescatore, Giovanna
    Laufer, Ralph
    Gonzalez-Paz, Odalys
    Di Marco, Annalise
    Fiore, Fabrizio
    Monteagudo, Edith
    Fonsi, Massimiliano
    Felock, Peter J.
    Rowley, Michael
    Summa, Vincenzo
    JOURNAL OF MEDICINAL CHEMISTRY, 2008, 51 (04) : 861 - 874