
CAS号:1970972-74-7
分子式: C16H20F3N5O4S 分子量: 435.42
产品形式: Free Base
研发状态: Completed
研发用途: Heart Failure With Reduced Ejection Fraction; Dilated Cardiomyopathy
研究机构: Bristol-Myers Squibb
研发日期: February 6 2018
研发阶段: Phase 1 : Phase 2
Danicamtiv (MYK-491, SAR 440181) is a novel cardiac myosin activator that enhances cardiomyocyte contraction.
中文名称: (S)-10-羟基喜树碱
CAS号:19685-09-7
分子式: C20H16N2O5 分子量: 364.35
产品形式: free base
研发状态: Recruiting
研发用途: Advanced Solid Tumor
研究机构: TaiRx Inc.
研发日期: October 31 2023
研发阶段: Phase 1
(S)-10-Hydroxycamptothecin (10-HCPT) is a DNA topoisomerase I inhibitor with potent anti-tumor activity.
中文名称: 雷美替胺
CAS号:196597-26-9
分子式: C16H21NO2 分子量: 259.34
产品形式: free base
研发状态: Completed
研发用途: Delirium
研究机构: Rhode Island Hospital
研发日期: May 9 2019
研发阶段: Phase 4
Ramelteon (TAK-375) is a novel melatonin receptor agonist for human MT1 and MT2 receptors and chick forebrain melatonin receptors with Ki of 14 pM, 112 pM and 23.1 pM, respectively.
中文名称:21-羟基-17-(1-氧代丙氧基)孕甾-4-烯-3,20-二酮
CAS号:19608-29-8
分子式: C24H34O5 分子量: 402.52
产品形式: free base
研发状态: Completed
研发用途: Healthy Volunteers
研究机构: Cassiopea SpA
研发日期: June 6 2018
研发阶段: Phase 1
Clascoterone (Winlevi, Cortexolone 17 alpha-propionate, Cortexolone 17α-propionate, CB-03-01) is a topical and peripherally selective antagonist of androgen receptor (AR).
中文名称:利米多赛
CAS号:195514-63-7
分子式: C78H98N4O20 分子量: 1411.63
产品形式: Free base
研发状态: Recruiting
研发用途: Brain Tumor Pediatric; Medulloblastoma Childhood; Embryonal Tumor; High Grade Glioma; Diffuse Midline Glioma; Diffuse Intrinsic Pontine Glioma; Brain Tumor Adult
研究机构: Bambino Gesù Hospital and Research Institute
研发日期: November 9 2023
研发阶段: Phase 1
Rimiducid (AP1903) is a chemical protein dimerizer and binds tightly to the target FKBP fusion protein while binding minimally to the abundant natural FKBP. Rimiducid elicites potent and dose-dependent apoptosis of cells in culture expressing dimerizer-dependent Fas constructs, with an EC50 of ≈0.1 nM.
CAS号:1952251-28-3
分子式: C17H21FN6.HCl 分子量: 380.85
产品形式: hydrochloride
研发状态: Withdrawn
研发用途: Lymphoma Non-Hodgkin
研究机构: Calithera Biosciences Inc; Nektar Therapeutics
研发日期: April 3 2019
研发阶段: Phase 1
TAK-659 is a potent and selective inhibitor of spleen tyrosine kinase (SYK) with an IC50 value of 3.2 nM. It is selective against most other kinases, but potent toward both SYK and FLT3.
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