
中文名称:苯甲丁氮酮
CAS号:42200-33-9
分子式: C17H27NO4 分子量: 309.40
产品形式: free base
研发状态: Completed
研发用途: Infantile Hemangioma
研究机构: The Hospital for Sick Children
研发日期: Nov-09
研发阶段: Phase 2
Nadolol (Corgard, Solgol, Anabet, SQ11725) is a non-selective beta-adrenergic antagonist with antihypertensive and antiarrhythmic activities.
中文名称:盐酸可乐定
CAS号:4205-91-8
分子式: C9H9Cl2N3.HCl 分子量: 266.50
产品形式: Hydrochloride
研发状态: Not yet recruiting
研发用途: Postoperative Pain
研究机构: Assiut University
研发日期: December 1 2023
研发阶段: Phase 1
Clonidine HCl(Kapvay) is a direct-acting α2 adrenergic agonist with an ED50 of 0.02±0.01 mg/kg.
中文名称:非诺贝特酸
CAS号:42017-89-0
分子式: C17H15ClO4 分子量: 318.75
产品形式: free base
研发状态: Completed
研发用途: Dyslipidemias
研究机构: Chong Kun Dang Pharmaceutical
研发日期: October 12 2017
研发阶段: Phase 1
Fenofibric acid (NSC 281318, Trilipix, FNF acid) is a fibrate that acts as a lipid-lowering agent, decreasing low-density lipoprotein cholesterol and triglycerides.
中文名称: 托利咪酮
CAS号:41964-07-2
分子式: C11H10N2O2 分子量: 202.21
产品形式: free base
研发状态: Completed
研发用途: Type 2 Diabetes
研究机构: Melior Pharmaceuticals; Bukwang Pharmaceutical Co. Ltd.
研发日期: Dec-14
研发阶段: Phase 2
MLR-1023 (Tolimidone, CP-26154) is a Lyn kinase activator and a novel insulin receptor potentiator that elicits a rapid-onset and durable improvement in glucose homeostasis in animal models of type 2 diabetes.
中文名称:苯扎贝特
CAS号:41859-67-0
分子式: C19H20ClNO4 分子量: 361.82
产品形式: free base
研发状态: Completed
研发用途: Acute Myocardial Infarction
研究机构: Instituto Mexicano del Seguro Social
研发日期: Jan-11
研发阶段: Phase 4
Bezafibrate (BM 15075) is the first clinically tested dual and pan-PPAR co-agonism.
中文名称:乐伐替尼
CAS号:417716-92-8
分子式: C21H19ClN4O4 分子量: 426.85
产品形式: free base
研发状态: Not yet recruiting
研发用途: Neoplasms
研究机构: National Cancer Institute (NCI); National Institutes of Health Clinical Center (CC)
研发日期: May 15 2024
研发阶段: Phase 1
Lenvatinib (E7080) is a multi-target inhibitor, mostly for VEGFR2(KDR)/VEGFR3(Flt-4) with IC50 of 4 nM/5.2 nM, less potent against VEGFR1/Flt-1, ~10-fold more selective for VEGFR2/3 against FGFR1, PDGFRα/β in cell-free assays. Lenvatinib (E7080) also inhibits FGFR1-4, PDGFR, Kit (c-Kit), RET (c-RET), and shows potent antitumor activities. Phase 3.
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