
中文名称:盐酸非索非那定
CAS号:153439-40-8
分子式: C32H39NO4.HCl 分子量: 538.12
产品形式: HCl
研发状态: Completed
研发用途: Drug Interaction Study
研究机构: Insel Gruppe AG University Hospital Bern; Bayer
研发日期: February 13 2019
研发阶段: Phase 1
Fexofenadine (MDL 16455A) inhibits histamine H1 receptor with IC50 of 246 nM.
CAS号:1532533-67-7
分子式: C31H24F3N5O3 分子量: 571.55
产品形式: free base
研发状态: Terminated
研发用途: Chronic Lymphocytic Leukemia; Non Hodgkin Lymphoma
研究机构: TG Therapeutics Inc.
研发日期: August 9 2017
研发阶段: Phase 2
Umbralisib (TGR-1202, Rp-5264), a novel, next generation PI3Kδ inhibitor, inhibits PI3Kδ activity in enzyme and cell based assays with IC50 and EC50 values of 22.2 & 24.3 nM, respectively.
中文名称:普可那利
CAS号:153168-05-9
分子式: C18H18F3N3O3 分子量: 381.35
产品形式: Free Base
研发状态: Completed
研发用途: Enterovirus Infection
研究机构: National Institute of Allergy and Infectious Diseases (NIAID)
研发日期: June 27 2001
研发阶段: Phase 2
Pleconaril (APO-P001, Picovir, VP 63843, WIN 63843) is a capsid inhibitor used previously to treat enterovirus infections. Pleconaril is effective in inhibiting replication with IC50 of < 0.050 μM.
中文名称:双氯芬酸钾
CAS号:15307-81-0
分子式: C14H10Cl2KNO2 分子量: 334.24
产品形式: Potassium
研发状态: Not yet recruiting
研发用途: Interaction
研究机构: Washington State University
研发日期: January 1 2024
研发阶段: Early Phase 1
Diclofenac potassium (CGP-45840B) is a nonsteroidal anti-inflammatory drug taken to reduce inflammation and as an analgesic reducing pain in certain conditions.
中文名称:双氯芬酸钠
CAS号:15307-79-6
分子式: C14H10Cl2NNaO2 分子量: 318.13
产品形式: Sodium Salt
研发状态: Not yet recruiting
研发用途: Interaction
研究机构: Washington State University
研发日期: January 1 2024
研发阶段: Early Phase 1
Diclofenac Sodium (GP 45840) is a non-selective COX inhibitor with IC50 of 0.5 μg/ml and 0.5 μg/ml for COX-1 and -2 in intact cells, respectively, used as a nonsteroidal anti-inflammatory drug (NSAID) to relieve pain and reduce swelling in flammation.
中文名称:盐酸奈必洛尔
CAS号:152520-56-4
分子式: C22H25F2NO4.HCl 分子量: 441.90
产品形式: Hydrochloride
研发状态: Recruiting
研发用途: Heart Failure
研究机构: Novartis Pharmaceuticals; Novartis
研发日期: April 4 2023
研发阶段: --
Nebivolol HCl (R-65824) selectively inhibits β1-adrenoceptor with IC50 of 0.8 nM.
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