
中文名称:4-(乙酰氨基)-3-[(4-氯苯基)硫代]-2-甲基-1H-吲哚-1-乙酸
CAS号:802904-66-1
分子式: C19H17ClN2O3S 分子量: 388.87
产品形式: free base
研发状态: Completed
研发用途: Type 2 Diabetes Mellitus
研究机构: AstraZeneca
研发日期: Mar-15
研发阶段: Phase 1
AZD1981 is a potent, selective CRTh2 (DP2) receptor antagonist with IC50 of 4 nM, showing >1000-fold selectivity over more than 340 other enzymes and receptors, including DP1. Phase 2.
中文名称:辛伐他汀,斯伐他汀
CAS号:79902-63-9
分子式: C25H38O5 分子量: 418.57
产品形式: free base
研发状态: Not yet recruiting
研发用途: Recurrent Acute Pancreatitis; Chronic Pancreatitis
研究机构: Cedars-Sinai Medical Center; United States Department of Defense
研发日期: Jan-24
研发阶段: Early Phase 1
Simvastatin (MK-0733, MK 733) is a competitive inhibitor of HMG-CoA reductase with Ki of 0.1-0.2 nM in cell-free assays. Simvastatin induces ferroptosis, mitophagy, autophagy and apoptosis.
中文名称:维生素A棕榈酸酯
CAS号:79-81-2
分子式: C36H60O2 分子量: 524.86
产品形式: Free Base
研发状态: Completed
研发用途: Dyslipidemia
研究机构: University Health Network Toronto
研发日期: Mar-12
研发阶段: Phase 3
Retinyl (Vitamin A) Palmitate is a more stable, synthetic version of the essential nutrient vitamin A joined to palmitic acid.
中文名称:氯雷他定
CAS号:79794-75-5
分子式: C22H23ClN2O2 分子量: 382.88
产品形式: free base
研发状态: Completed
研发用途: Pruritus; Uremia; Chronic Kidney Diseases
研究机构: King Edward Medical University
研发日期: May 1 2022
研发阶段: Phase 4
Loratadine (Alavert,Claritin,SCH29851) is a histamine H1 receptor antagonist, used to treat allergies. Also acts as a selective inhibitor of B(0)AT2 with IC50 of 4 μM.
中文名称:左炔诺孕酮
CAS号:797-63-7
分子式: C21H28O2 分子量: 312.45
产品形式: free base
研发状态: Recruiting
研发用途: Healthy Participants
研究机构: Incyte Corporation
研发日期: May 7 2024
研发阶段: Phase 1
Levonorgestrel (D-Norgestrel) is a female hormone that prevents ovulation.
中文名称:利尼伐尼
CAS号:796967-16-3
分子式: C21H18FN5O 分子量: 375.41
产品形式: free base
研发状态: Completed
研发用途: Advanced Solid Tumors
研究机构: Abbott
研发日期: May-11
研发阶段: Phase 1
Linifanib (ABT-869, AL39324, RG3635) is a novel, potent ATP-competitive VEGFR/PDGFR inhibitor for KDR, CSF-1R, Flt-1/3 and PDGFRβ with IC50 of 4 nM, 3 nM, 3 nM/4 nM and 66 nM respectively, mostly effective in mutant kinase-dependent cancer cells (i.e. FLT3). Linifanib (ABT-869) induces autophagy and apoptosis. Phase 3.
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