
中文名称:维生素B6
CAS号:65-23-6
分子式: C8H11NO3 分子量: 169.18
产品形式: free base
研发状态: Not yet recruiting
研发用途: Dietary Exposure; Diabetes Mellitus Type 2; Cardiovascular Diseases; Bone Loss; Sustainability; Exposure; Obesity; Vitamin Deficiency; Mineral Deficiency
研究机构: German Federal Institute for Risk Assessment; Max Rubner-Institut; University of Bonn; Research Institute for Plant-Based Nutrition; University of Jena; University of Regensburg; Heidelberg University; University of Vienna
研发日期: April 1 2024
研发阶段: --
Pyridoxine (Pyridoxol, Vitamin B6, Gravidox), also known as vitamin B6, is a form of vitamin B6 found commonly in food and used as dietary supplement. It is a cofactor for both glutamic acid decarboxylase and GABA transaminase.
中文名称:吡哆醛盐酸盐
CAS号:65-22-5
分子式: C8H10ClNO3 分子量: 203.62
产品形式: Free Base
研发状态: Recruiting
研发用途: Prader-Willi Syndrome
研究机构: Harmony Biosciences LLC
研发日期: April 30 2024
研发阶段: Phase 3
Pyridoxal hydrochloride (HQ) is an active endogenous metabolite.
中文名称:尼可地尔
CAS号:65141-46-0
分子式: C8H9N3O4 分子量: 211.17
产品形式: free base
研发状态: Active not recruiting
研发用途: Chronic Stable Angina
研究机构: Auxilius Pharma sp.z.o.o.
研发日期: November 27 2023
研发阶段: Early Phase 1
Nicorandil (SG-75) is a potassium channel activator, and stimulates guanylate cyclase to increase formation of cyclic GMP (cGMP).
中文名称:丙氨酸布立尼布
CAS号:649735-63-7
分子式: C22H24FN5O4 分子量: 441.46
产品形式: Alaninate
研发状态: Completed
研发用途: Solid Tumors
研究机构: Bristol-Myers Squibb
研发日期: Oct-07
研发阶段: Phase 1
Brivanib alaninate (BMS-582664) is the prodrug of BMS-540215, an ATP-competitive inhibitor against VEGFR2 with IC50 of 25 nM.
中文名称: 布立尼布
CAS号:649735-46-6
分子式: C19H19FN4O3 分子量: 370.38
产品形式: free base
研发状态: Unknown status
研发用途: Ovarian Cancer
研究机构: Hunan Cancer Hospital
研发日期: January 14 2019
研发阶段: Phase 1
Brivanib is an ATP-competitive inhibitor against VEGFR2 with IC50 of 25 nM, moderate potency against VEGFR-1 and FGFR-1, but >240-fold against PDGFR-β. Phase 3.
中文名称:盐酸乌拉地尔
CAS号:64887-14-5
分子式: C20H29N5O3.HCl 分子量: 423.94
产品形式: Hydrochloride
研发状态: Unknown status
研发用途: Anesthesia
研究机构: Nan Jiang; First Affiliated Hospital Sun Yat-Sen University
研发日期: January 1 2016
研发阶段: Not Applicable
Urapidil HCl is a hydrochloride salt form of urapidil which is α1-adrenoceptor antagonist and 5-HT1A receptor agonist with pIC50 of 6.13 and 6.4 respectively.
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