
中文名称:5-(氨基磺酰基)-4-氯-2-(呋喃-2-基甲基)邻氨基苯甲酸钠
CAS号:41733-55-5
分子式: C12H10ClN2NaO5S 分子量: 352.73
产品形式: Sodium
研发状态: Recruiting
研发用途: Amyloidosis; Amyloidosis Cardiac; ATTR Amyloidosis Wild Type
研究机构: Paolo Milani; IRCCS Policlinico S. Matteo
研发日期: January 26 2024
研发阶段: --
Furosemide (Frusemide) sodium is a potent and orally active inhibitor of Na-K-Cl cotransporter (NKCC). Furosemide sodium is a subtype-selective antagonist of gamma-aminobutyric acid type A (GABAA) receptor.
中文名称:环吡酮胺
CAS号:41621-49-2
分子式: C12H17NO2.C2H7NO 分子量: 268.35
产品形式: Ethanolamine
研发状态: Completed
研发用途: Hematologic Malignancy; Acute Lymphocytic Leukemia; Chronic Lymphocytic Leukemia; Myelodysplasia; Acute Myeloid Leukemia; Chronic Myelogenous Leukemia; Hodgkin''s Disease
研究机构: University Health Network Toronto; The Leukemia and Lymphoma Society
研发日期: Oct-09
研发阶段: Phase 1
Ciclopirox ethanolamine (Ciclopirox olamine, HOE 296,Ciclopiroxolamine) is a broad-spectrum antifungal agent working as an iron chelator.
CAS号:415903-37-6
分子式: C26H29N5O3S 分子量: 491.61
产品形式: Free Base
研发状态: Terminated
研发用途: Non-small Cell Lung Cancer Adenocarcinoma
研究机构: Arrys Therapeutics; Merck Sharp & Dohme LLC
研发日期: January 8 2019
研发阶段: Phase 1 : Phase 2
Grapiprant (CJ-023,423, AT-001, AAT-007, RQ-00000007, CJ-23423) is a novel selective EP4 Prostaglandin Receptor inhibitor with Ki of 20 nM and 13 nM for rat EP4 receptor and human EP4 receptor, respectively.
中文名称:5-磷酸吡哆醛
CAS号:41468-25-1
分子式: C8H10NO6P.H2O 分子量: 265.16
产品形式: hydrate
研发状态: Completed
研发用途: Pyridoxine Dependant Epilepsy
研究机构: Vitaflo International Ltd; Radboud University Medical Center; Great Ormond Street Hospital for Children NHS Foundation Trust
研发日期: June 1 2021
研发阶段: Not Applicable
Pyridoxal 5-phosphate monohydrate is an active vitamin B6 metabolite, which is a cofactor in many reactions of amino acid metabolism.
中文名称:阿法骨化醇
CAS号:41294-56-8
分子式: C27H44O2 分子量: 400.64
产品形式: free base
研发状态: Completed
研发用途: Cardiac Valve Replacement Complication
研究机构: Cairo University
研发日期: April 1 2017
研发阶段: Phase 4
Alfacalcidol (1-hydroxycholecalciferol) is a non-selective VDR activator medication.
中文名称:盐酸美金刚
CAS号:41100-52-1
分子式: C12H21N.HCl 分子量: 215.76
产品形式: Hydrochloride
研发状态: Recruiting
研发用途: Neurocognitive Dysfunction
研究机构: Tata Memorial Centre
研发日期: February 22 2024
研发阶段: Phase 3
Memantine HCl is an antagonist of NMDAR. It is also a CYP2B6 and CYP2D6 inhibitor for recombinant CYP2B6 and CYP2D6 with IC50 of 1.12 μM and 242.4 μM, Ki of 0.51 μM and 84.4 μM, respectively.
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