
中文名称:阿帕利酮
CAS号:945966-46-1
分子式: C17H17FN2O4S 分子量: 364.39
产品形式: Free base
研发状态: Completed
研发用途: Healthy
研究机构: Mitsubishi Tanabe Pharma Corporation
研发日期: Jun-15
研发阶段: Phase 1
Apararenone (MT-3995) is a selective, long-acting nonsteroidal mineralocorticoid receptors (MR) antagonist.
中文名称:(2S)-N-[4-[2-[[4-(4-吗啉基)苯基]氨基]-4-嘧啶基]苯基]-2-吡咯烷甲酰胺
CAS号:945755-56-6
分子式: C25H28N6O2 分子量: 444.53
产品形式: free base
研发状态: Terminated
研发用途: Polycythemia Vera
研究机构: Exelixis
研发日期: Dec-07
研发阶段: Phase 1
XL019 is a potent and selective JAK2 inhibitor with IC50 of 2.2 nM, exhibiting >50-fold selectivity over JAK1, JAK3 and TYK2. Phase 1.
中文名称:莪术醇.姜黄醇
CAS号:945595-80-2
分子式: C28H21N7OS 分子量: 503.58
产品形式: free base
研发状态: Completed
研发用途: Cancer; Hematologic Malignancies; Leukemia; Myeloid Leukemia
研究机构: Amgen
研发日期: October 4 2011
研发阶段: Phase 1
AMG 900 is a potent and highly selective pan-Aurora kinases inhibitor for Aurora A/B/C with IC50 of 5 nM/4 nM /1 nM. It is >10-fold selective for Aurora kinases than p38α, Tyk2, JNK2, Met and Tie2. Phase 1.
中文名称:5-乙基磺酰基-2-萘-2-基-1,3-苯并恶唑
CAS号:945531-77-1
分子式: C19H15NO3S 分子量: 337.39
产品形式: free base
研发状态: Terminated
研发用途: Duchenne Muscular Dystrophy
研究机构: Summit Therapeutics
研发日期: Jun-16
研发阶段: Phase 2
Ezutromid (SMT C1100,BMN 195,VOX-C1100) is a first-in-class, orally active benzoxazole utrophin modulator with an EC50 of 0.91 μM which can be used for the research Duchenne muscular dystrophy (DMD), also inhibits CYP1A2 enzymic activity in human liver microsomes (HLM) with an IC50 of 5.4 μM.
中文名称:他米巴罗汀
CAS号:94497-51-5
分子式: C22H25NO3 分子量: 351.44
产品形式: free base
研发状态: Recruiting
研发用途: Acute Myeloid Leukemia
研究机构: Syros Pharmaceuticals
研发日期: August 26 2021
研发阶段: Phase 2
Tamibarotene(Am 80) is a synthetic retinoic acid receptor (RAR) agonist with high specificity for RARα and RARβ over RARγ.
中文名称:Decernotinib(VX-509)抑制剂
CAS号:944842-54-0
分子式: C18H19F3N6O 分子量: 392.38
产品形式: free base
研发状态: Completed
研发用途: Drug Interactions
研究机构: Vertex Pharmaceuticals Incorporated
研发日期: Jun-13
研发阶段: Phase 1
Decernotinib (VX-509) is a potent and selective JAK3 inhibitor with Ki of 2.5 nM, >4-fold selectivity over JAK1, JAK2, and TYK2, respectively. Phase 2/3.
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