
中文名称:布列奎钠
CAS号:96201-88-6
分子式: C23H14F2NNaO2 分子量: 397.35
产品形式: Sodium
研发状态: Recruiting
研发用途: Functional Abdominal Pain Syndrome
研究机构: Karolinska Institutet; Child and Adolescent Psychiatry Stockholm
研发日期: November 1 2023
研发阶段: --
Brequinar Sodium (Bipenquinate, BRQ, DUP-785, NSC 368390) is a potent and selective dihydroorotate dehydrogenase (DHODH) inhibitor with IC50 of ~20 nM and triggers differentiation in the ER-HoxA9, U937, and THP1 cells with ED50 of ~1 μM.
中文名称:达普司他
CAS号:960539-70-2
分子式: C19H27N3O6 分子量: 393.43
产品形式: free base
研发状态: Recruiting
研发用途: Anaemia
研究机构: GlaxoSmithKline
研发日期: September 6 2023
研发阶段: Phase 3
Daprodustat (GSK1278863) is an orally administered hypoxia-inducible factor-prolyl hydroxylase (HIF-PH) inhibitor. Phase 2.
中文名称: 美罗培南
CAS号:96036-03-2
分子式: C17H25N3O5S 分子量: 383.46
产品形式: free base
研发状态: Not yet recruiting
研发用途: Cardiogenic Shock; Post-cardiac Surgery; Cardiac Arrest; Extracorporeal Membrane Oxygenation Complication; Infections
研究机构: University Hospital Grenoble
研发日期: September 1 2024
研发阶段: Not Applicable
Meropenem (SM 7338) is an ultra-broad spectrum injectable antibiotic.
中文名称:依氟鸟氨酸盐酸盐一水合物
CAS号:96020-91-6
分子式: C6H12F2N2O2.HCl.H2O 分子量: 236.64
产品形式: hydrochloride hydrate
研发状态: Recruiting
研发用途: Type 1 Diabetes
研究机构: Emily K. Sims; Juvenile Diabetes Research Foundation; Cancer Prevention Pharmaceuticals Inc.; Indiana University
研发日期: March 14 2023
研发阶段: Phase 2
Eflornithine (Difluoromethylornithine, DFMO, MDL-71782, RMI-71782, α-difluoromethylornithine) hydrochloride hydrate inhibits polyamine biosynthesis by the selective, irreversible inhibition of ornithine decarboxylase (ODC). A chemoprotective agent that blocks angiogenesis. Its biological half-life is 8 hours.
中文名称: 盐酸索他洛尔
CAS号:959-24-0
分子式: C12H20N2O3S.HCl 分子量: 308.82
产品形式: Hydrochloride
研发状态: Completed
研发用途: Atrial Arrhythmia
研究机构: University of Utah; AltaThera Pharmaceuticals LLC
研发日期: February 4 2022
研发阶段: --
Sotalol(MJ-1999) is a non-selective beta blocker and a potassium channel blocker with an IC50 of 43 μM.
中文名称:(5Z)-5-[[4-(4-吡啶基)-6-喹啉基]亚甲基]-2,4-噻唑烷二酮
CAS号:958852-01-2
分子式: C18H11N3O2S 分子量: 333.36
产品形式: Free Base
研发状态: Terminated
研发用途: Solid Tumours
研究机构: GlaxoSmithKline
研发日期: June 24 2008
研发阶段: Phase 1
GSK1059615 is a dual inhibitor of PI3Kα/β/δ/γ (reversible) and mTOR with IC50 of 0.4 nM/0.6 nM/2 nM/5 nM and 12 nM, respectively. Phase 1.
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