
中文名称:瑞格列奈
CAS号:135062-02-1
分子式: C27H36N2O4 分子量: 452.59
产品形式: free base
研发状态: Recruiting
研发用途: Healthy Volunteers
研究机构: Takeda
研发日期: March 29 2024
研发阶段: Phase 1
Repaglinide (AG-EE 623 ZW) is a potassium channel blocker, which lowers blood glucose by stimulating the release of insulin from the pancreas, used the treatment of type II diabetes.
中文名称: 格拉瑞韦
CAS号:1350514-68-9
分子式: C38H50N6O9S 分子量: 766.90
产品形式: free base
研发状态: Withdrawn
研发用途: HCV
研究机构: Fundacion SEIMC-GESIDA
研发日期: July 1 2017
研发阶段: Phase 4
Grazoprevir anhydrous (MK5172) is a Hepatitis C Virus NS3/4A Protease inhibitor with IC50 values of 7pM, 4pM, and 62pM for HCV genotype 1a, 1B, and 4 respectively.
CAS号:1349719-98-7
分子式: C27H34ClN7OS 分子量: 540.13
产品形式: chloride
研发状态: Terminated
研发用途: Advanced Ovarian Cancer; Triple Negative Breast Cancer
研究机构: Hoffmann-La Roche
研发日期: November 8 2017
研发阶段: Phase 1
TEN-010 (RG6146, Ro-6870810,(S)-JQ-35) is an inhibitor of the Bromodomain and Extra-Terminal(BET) family bromodomain-containing proteins with potential antineoplastic activity.
中文名称:拉米夫定
CAS号:134678-17-4
分子式: C8H11N3O3S 分子量: 229.26
产品形式: free base
研发状态: Recruiting
研发用途: Retinal Detachment; Rhegmatogenous Retinal Detachment
研究机构: University of Wisconsin Madison
研发日期: January 30 2024
研发阶段: Early Phase 1
Lamivudine (BCH-189, GR109714X) is a potent nucleoside analog reverse transcriptase inhibitor, used for treatment of chronic HBV and HIV/AIDS. It works by blocking the HIV reverse transcriptase and hepatitis B virus polymerase.
中文名称:(2R,3S)-2-[4-(环戊基氨基)苯基]-1-(2-氟-6-甲基苯甲酰基)-N-[4-甲基3-(三氟甲基)苯基]哌啶-3-甲酰胺
CAS号:1346623-17-3
分子式: C33H35F4N3O2 分子量: 581.64
产品形式: Free Base
研发状态: Not yet recruiting
研发用途: Vasculitis
研究机构: Amgen
研发日期: July 31 2024
研发阶段: Phase 3
Avacopan (CCX168) is an orally administered and selective C5a receptor (C5aR) antagonist.
中文名称:EZH2甲基转移酶抑制剂(GSK126)
CAS号:1346574-57-9
分子式: C31H38N6O2 分子量: 526.67
产品形式: Free Base
研发状态: Terminated
研发用途: Cancer; Neoplasms
研究机构: GlaxoSmithKline
研发日期: April 24 2014
研发阶段: Phase 1
GSK126 (GSK2816126A, GSK2816126) is a potent, highly selective EZH2 methyltransferase inhibitor with IC50 of 9.9 nM, >1000-fold selective for EZH2 over 20 other human methyltransferases.
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