
中文名称: 氨溴索
CAS号:18683-91-5
分子式: C13H18Br2N2O 分子量: 378.10
产品形式: Expectorant
研发状态: Not yet recruiting
研发用途: Lewy Body Disease
研究机构: Lawson Health Research Institute
研发日期: Jan-25
研发阶段: Phase 1 : Phase 2
Ambroxol, a substituted benzylamine, is an active metabolite of bromhexine. It is a potent inhibitor of the neuronal Na+ channels.
中文名称:盐酸莫西沙星
CAS号:186826-86-8
分子式: C21H24FN3O4.HCl 分子量: 437.89
产品形式: Hydrochloride
研发状态: Recruiting
研发用途: Healthy
研究机构: Boehringer Ingelheim
研发日期: March 4 2024
研发阶段: Phase 1
Moxifloxacin (Avelox, Avalox,BAY12-8039 HCl) is a fourth-generation synthetic fluoroquinolone antibacterial agent.
中文名称:[(1S)-1-氰基-2-甲基丙基]氨基甲酸苄酯
CAS号:186692-46-6
分子式: C19H26N6O 分子量: 354.45
产品形式: free base
研发状态: Terminated
研发用途: Cystic Fibrosis
研究机构: University Hospital Brest; ManRos Therapeutics; Cyclacel Pharmaceuticals Inc.
研发日期: February 22 2016
研发阶段: Phase 2
Roscovitine (CYC202, Seliciclib, R-roscovitine) is a potent and selective CDK inhibitor for Cdc2, CDK2 and CDK5 with IC50 of 0.65 μM, 0.7 μM and 0.16 μM in cell-free assays. It shows little effect on CDK4/6. Phase 2.
中文名称:2-(4-(1,3,4-噁二唑-2-基)苯基)-N-(3-甲氧基-5-甲基吡嗪-2-基)吡啶-3-磺酰胺
CAS号:186497-07-4
分子式: C19H16N6O4S 分子量: 424.43
产品形式: free base
研发状态: Terminated
研发用途: Prostate Cancer
研究机构: University of Wisconsin Madison; AstraZeneca
研发日期: Apr-10
研发阶段: Phase 2
Zibotentan (ZD4054) is a specific Endothelin (ET)A antagonist with IC50 of 21 nM, exhibiting no activity at ETB. Phase 3.
CAS号:1860875-51-9
分子式: C22H18ClF2N3O4 分子量: 461.85
产品形式: Free Base
研发状态: Active not recruiting
研发用途: Leukemia Myeloid Acute; Myelodysplastic Syndromes
研究机构: Celgene
研发日期: November 14 2016
研发阶段: Phase 1
CC-90009 is a novel cereblon (CRBN) E3 ligase modulator and specifically targets GSPT1 (G1 to S phase transition 1) for proteasomal degradation.
中文名称:[(1R,2S,4R)-4-[[5-[[5-[4-((1R)-7-氯-1,2,3,4-四氢异喹啉-1-基)-5-甲基噻吩-2-基]羰基]嘧啶-4-基]氨基]-2-羟基环戊基]甲基磺酸甲酯
CAS号:1858276-04-6
分子式: C25H28ClN5O5S2 分子量: 578.10
产品形式: Free base
研发状态: Active not recruiting
研发用途: Advanced or Metastatic Solid Tumors
研究机构: Takeda; Takeda Development Center Americas Inc.
研发日期: August 17 2020
研发阶段: Phase 1 : Phase 2
Subasumstat (TAK-981) is a novel, selective inhibitor of the SUMOylation enzymatic cascade with potential immune-activating and antineoplastic activities.
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