The Discovery of GSK3640254, a Next-Generation Inhibitor of HIV-1 Maturation

被引:8
|
作者
Regueiro-Ren, Alicia [7 ]
Sit, Sing-Yuen [1 ]
Chen, Yan [1 ]
Chen, Jie [1 ]
Swidorski, Jacob J. [1 ]
Liu, Zheng [1 ]
Venables, Brian L. [1 ]
Sin, Ny [1 ]
Hartz, Richard A. [1 ]
Protack, Tricia [2 ]
Lin, Zeyu [2 ]
Zhang, Sharon [2 ]
Li, Zhufang [2 ]
Wu, Dauh-Rurng [3 ]
Li, Peng [3 ]
Kempson, James [1 ,3 ]
Hou, Xiaoping [1 ,3 ]
Gupta, Anuradha
Rampulla, Richard [3 ]
Mathur, Arvind
Park, Hyunsoo [4 ]
Sarjeant, Amy [4 ]
Benitex, Yulia [5 ]
Rahematpura, Sandhya [5 ]
Parker, Dawn [5 ]
Phillips, Thomas [5 ]
Haskell, Roy [5 ]
Jenkins, Susan [5 ]
Santone, Kenneth S. [5 ]
Cockett, Mark [2 ]
Hanumegowda, Umesh [5 ]
Dicker, Ira [2 ]
Meanwell, Nicholas A. [7 ]
Krystal, Mark [2 ,6 ]
机构
[1] Bristol Myers Squibb Res & Early Dev, Dept Discovery Chem, Wallingford, CT 06492 USA
[2] Bristol Myers Squibb Res & Early Dev, Dept Virol, Wallingford, CT 06492 USA
[3] Bristol Myers Squibb Res & Early Dev, Dept Discovery Synth, Princeton, NJ 08543 USA
[4] Bristol Myers Squibb Chem & Synthet Dev, New Brunswick, NJ 08901 USA
[5] Bristol Myers Squibb Res & Early Dev, Dept Pharmaceut Candidate Optimizat, Wallingford, CT 06492 USA
[6] ViiV Healthcare, 36 East Ind Rd, Branford, CT 06405 USA
[7] Bristol Myers Squibb Res & Early Dev, Small Mol Drug Discovery, Princeton, NJ 08543 USA
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; CONVENIENT REAGENT; ACYL GLUCURONIDES; ACID-DERIVATIVES; BETULINIC ACID; BEVIRIMAT; 1,3-DIOXIN-4-ONES; REPLICATION; BMS-955176; GSK3532795;
D O I
10.1021/acs.jmedchem.2c00879
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
GSK3640254 is an HIV-1 maturation inhibitor (MI) that exhibits significantly improved antiviral activity toward a range of clinically relevant polymorphic variants with reduced sensitivity toward the second-generation MI GSK3532795 (BMS-955176). The key structural difference between GSK3640254 and its predecessor is the replacement of the para-substituted benzoic acid moiety attached at the C-3 position of the triterpenoid core with a cyclohex-3-ene-1-carboxylic acid substituted with a CH2F moiety at the carbon atom alpha- to the pharmacophoric carboxylic acid. This structural element provided a new vector with which to explore structure-activity relationships (SARs) and led to compounds with improved polymorphic coverage while preserving pharmacokinetic (PK) properties. The approach to the design of GSK3640254, the development of a synthetic route and its preclinical profile are discussed. GSK3640254 is currently in phase IIb clinical trials after demonstrating a dose-related reduction in HIV-1 viral load over 7-10 days of dosing to HIV-1-infected subjects.
引用
收藏
页码:11927 / 11948
页数:22
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