
中文名称: 溴化新斯的明
CAS号:114-80-7
分子式: C12H19N2O2.Br 分子量: 303.20
产品形式: Bromide
研发状态: Not yet recruiting
研发用途: Neuromuscular Blocks
研究机构: The Cleveland Clinic; Merck Sharp & Dohme LLC
研发日期: May 15 2024
研发阶段: Not Applicable
Neostigmine Bromide is a reversible acetylcholinesterase inhibitor.
中文名称:氯沙坦
CAS号:114798-26-4
分子式: C22H23ClN6O 分子量: 422.91
产品形式: free base
研发状态: Recruiting
研发用途: Healthy
研究机构: University of Electronic Science and Technology of China
研发日期: March 5 2024
研发阶段: Not Applicable
Losartan(DuP-753) is a selective, orally administered, nonpeptide blocker of angiotensin II type 1 (AT1) receptor used to treat high blood pressure, diabetic kidney disease, heart failure, and left ventricular enlargement.
中文名称:塞来西布
CAS号:1146699-66-2
分子式: C20H17ClF4N4O4S 分子量: 520.88
产品形式: free base
研发状态: Completed
研发用途: Alzheimer Disease
研究机构: Bristol-Myers Squibb; PRA Health Sciences
研发日期: Aug-10
研发阶段: Phase 1
Avagacestat (BMS-708163) is a potent, selective, orally bioavailable γ-secretase inhibitor of Aβ40 and Aβ42 with IC50 of 0.3 nM and 0.27 nM, demonstrating a 193-fold selectivity against Notch. Phase 2.
中文名称:氢溴酸东莨菪碱
CAS号:114-49-8
分子式: C17H21NO4.HBr 分子量: 384.26
产品形式: Hydrobromide
研发状态: Recruiting
研发用途: Post-operative Nausea and Vomiting
研究机构: Milton S. Hershey Medical Center
研发日期: February 1 2024
研发阶段: Phase 2
Scopolamine HBr (LSM-4015,NSC 61806,(-)-Scopolamine hydrobromide, Hyoscine hydrobromide, Scopine hydrobromide) is a competitive muscarinic acetylcholine receptor antagonist with an IC50 of 55.3 nM.
中文名称:尿石素A
CAS号:1143-70-0
分子式: C13H8O4 分子量: 228.20
产品形式: free base
研发状态: Recruiting
研发用途: Healthy Volunteer
研究机构: National Institute on Aging (NIA); National Institutes of Health Clinical Center (CC)
研发日期: May 15 2024
研发阶段: Not Applicable
Urolithin A (3,8-Dihydroxy Urolithin, 2',7-Dihydroxy-3,4-benzocoumarin), a metabolite of ellagitannin, is a first-in-class natural compound that induces mitophagy both in vitro and in vivo following oral consumption.
中文名称:(S)-4-氨基-N-(1-(4-氯苯基)-3-羟基丙基)-1-(7H-吡咯并[2,3-d]嘧啶-4-基)哌啶-4-羧酰胺
CAS号:1143532-39-1
分子式: C21H25ClN6O2 分子量: 428.92
产品形式: free base
研发状态: Completed
研发用途: Breast Cancer; Prostate Cancer; Advanced Solid Tumors
研究机构: Memorial Sloan Kettering Cancer Center
研发日期: October 11 2017
研发阶段: Phase 1
Capivasertib (AZD5363) potently inhibits all isoforms of Akt(Akt1/Akt2/Akt3) with IC50 of 3 nM/8 nM/8 nM in cell-free assays, similar to P70S6K/PKA and lower activity towards ROCK1/2. Phase 2.
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