
中文名称:克立硼罗
CAS号:906673-24-3
分子式: C14H10BNO3 分子量: 251.05
产品形式: free base
研发状态: Completed
研发用途: Atopic Dermatitis; Atopic Dermatitis Eczema
研究机构: University of California Irvine; Pfizer
研发日期: March 23 2021
研发阶段: Early Phase 1
Crisaborole (AN2728) is a small-molecule, boron-based, selective PDE4 inhibitor and has broad-spectrum anti-inflammatory activity.
中文名称:(3R,4R)-3-(5,6-二氢-4H-吡咯并[3,2,1-IJ]喹啉-1-基)-4-(1H-吲哚-3-基)吡咯烷-2,5-二酮
CAS号:905854-02-6
分子式: C23H19N3O2 分子量: 369.42
产品形式: free base
研发状态: Completed
研发用途: Hepatic Impairment; Solid Tumor; Cancer
研究机构: Daiichi Sankyo; Medpace Inc.
研发日期: Apr-14
研发阶段: Phase 1
Tivantinib (ARQ 197) is the first non-ATP-competitive c-Met inhibitor with Ki of 0.355 μM in a cell-free assay, little activity to Ron, and no inhibition to EGFR, InsR, PDGFRα or FGFR1/4. Tivantinib (ARQ 197) induces a G2/M arrest and apoptosis.
中文名称:氨基磺酸 [(1S,2S,4R)-4-[4-[[(1S)-2,3-二氢-1H-茚-1-基]氨基]-7H-吡咯并[2,3-d]嘧啶-7-基]-2-羟基环戊基]甲基酯
CAS号:905579-51-3
分子式: C21H25N5O4S 分子量: 443.52
产品形式: Free base
研发状态: Withdrawn
研发用途: Myelodysplastic Syndromes (MDS)
研究机构: Takeda
研发日期: October 1 2021
研发阶段: Phase 2
MLN4924 is a small molecule inhibitor of Nedd8 activating enzyme (NAE) with IC50 of 4 nM.
中文名称:1-[3-[3-(4-氯丙基)丙氧基]丙基]-哌啶盐酸盐
CAS号:903576-44-3
分子式: C17H27Cl2NO 分子量: 332.31
产品形式: hydrochloride
研发状态: Active not recruiting
研发用途: Idiopathic Hypersomnia; Excessive Daytime Sleepiness
研究机构: Harmony Biosciences LLC
研发日期: August 19 2022
研发阶段: Phase 3
Pitolisant (Tiprolisant, BF-2649) acts as a high-affinity competitive antagonist (Ki=0.16 nM) and as an inverse agonist (EC50=1.5 nM) at the human histamine H3 receptor subtype.
中文名称:比卡鲁胺
CAS号:90357-06-5
分子式: C18H14F4N2O4S 分子量: 430.37
产品形式: free base
研发状态: Not yet recruiting
研发用途: Carcinoma Renal Cell
研究机构: State University of New York at Buffalo
研发日期: June 1 2024
研发阶段: Phase 1 : Phase 2
Bicalutamide (ICI-176334) is an androgen receptor (AR) antagonist with IC50 of 0.16 μM in LNCaP/AR(cs)cell line. Bicalutamide promotes autophagy.
中文名称:2-氨基-1,4-二氢-4-氧代蝶啶-6-羧酸
CAS号:902135-91-5
分子式: C16H18Cl3N5O2 分子量: 418.71
产品形式: Hydrochloride
研发状态: Completed
研发用途: Multiple Myeloma
研究机构: Astex Pharmaceuticals Inc.; Multiple Myeloma Research Consortium
研发日期: Nov-10
研发阶段: Phase 1 : Phase 2
AT7519 HCl is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of 10-210 nM in cell-free assays. It is less potent to CDK3 and little active to CDK7. Phase 2.
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