
CAS号:1236699-92-5
分子式: C15H15FIN3O3 分子量: 431.20
产品形式: free base
研发状态: Completed
研发用途: Neoplasm Malignant
研究机构: Sanofi; Merck KGaA Darmstadt Germany
研发日期: Nov-13
研发阶段: Phase 1
Pimasertib (AS-703026, MSC1936369B, SAR 245509) is a highly selective, potent, ATP non-competitive allosteric inhibitor of MEK1/2 with IC50 of 5 nM-2 μM in MM cell lines. Phase 2.
中文名称:利阿米洛韦
CAS号:123606-06-4
分子式: C5H4N6O3S 分子量: 228.19
产品形式: free base
研发状态: Terminated
研发用途: Covid19
研究机构: Wits Health Consortium (Pty) Ltd; PharmaCentrix (Pty) Ltd; Perinatal HIV Research Unit of the University of the Witswatersrand
研发日期: September 8 2020
研发阶段: Phase 2 : Phase 3
Riamilovir (Triazavirin) is a broad-spectrum antiviral drug candidate, which can be used for potential application against the Coronavirus 2019-nCoV.
中文名称:LY2608204 (1R,2S)-2-环己基-1-(4-(环丙基磺酰基)苯基)-N-(5-((2-(吡咯烷-1-基)乙基)硫代)噻唑-2-基)环丙烷羧酰胺
CAS号:1234703-40-2
分子式: C28H37N3O3S3 分子量: 559.81
产品形式: free base
研发状态: Withdrawn
研发用途: Diabetes Mellitus Type 2
研究机构: Eli Lilly and Company
研发日期: Sep-11
研发阶段: Phase 2
LY2608204 activates glucokinase (GK) with EC50 of 42 nM. Phase 2.
中文名称: 利凡斯的明
CAS号:123441-03-2
分子式: C14H22N2O2 分子量: 250.34
产品形式: free base
研发状态: Recruiting
研发用途: Depressive Disorder
研究机构: UMC Utrecht; ZonMw: The Netherlands Organisation for Health Research and Development; St. Antonius Hospital; Tergooi Hospital
研发日期: September 29 2021
研发阶段: Phase 4
Rivastigmine (SDZ-ENA 713, Exelon) is a cholinesterase inhibitor with IC50 of 5.5 μM. It inhibits acetylcholinesterase (IC50 = 4.15 µM) and butyrylcholinesterase (IC50 = 37 nM).
CAS号:1234015-54-3
分子式: C18H19N7O2.2HCl 分子量: 438.31
产品形式: dihydrochloride
研发状态: Active not recruiting
研发用途: Desmoplastic Small Round Cell Tumor; Rhabdomyosarcoma
研究机构: Memorial Sloan Kettering Cancer Center
研发日期: September 17 2019
研发阶段: Phase 1 : Phase 2
Prexasertib (LY2606368) is an ATP-competitive CHK1 inhibitor with a Ki value of 0.9 nmol/L. For CHK2 and RSK, its IC50 values are 8 nM and 9 nM respectively in cell-free assay.
中文名称:普瑞色替
CAS号:1234015-52-1
分子式: C18H19N7O2 分子量: 365.39
产品形式: Free base
研发状态: Active not recruiting
研发用途: Desmoplastic Small Round Cell Tumor; Rhabdomyosarcoma
研究机构: Memorial Sloan Kettering Cancer Center
研发日期: September 17 2019
研发阶段: Phase 1 : Phase 2
Prexasertib (LY2606368, ACR 368) is a selective ATP competitor inhibitor of Chk1 and Chk2 with IC50s of 1 nM and 8 nM in cell-free assays, respectively. Prexasertib also inhibits RSK1 with an IC50 of 9 nM in cell-free assay.
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