
中文名称:亚胺培南(一水物)
CAS号:74431-23-5
分子式: C12H17N3O4S.H2O 分子量: 317.36
产品形式: hydrate
研发状态: Recruiting
研发用途: Cystic Fibrosis; Pneumonia Bacterial
研究机构: Hartford Hospital; Merck Sharp & Dohme LLC; Q2 Solutions; Connecticut Children''s Medical Center; St. Christopher''s Hospital for Children; University of Texas Southwestern Medical Center; University of Pittsburgh Medical Center; Indiana University Health Methodist Hospital; James Whitcomb Riley Hospital for Children
研发日期: January 3 2023
研发阶段: Phase 4
Imipenem acts as an inhibitor of AmpC β-lactamase and is an antibiotic useful for the treatment of a number of bacterial infections.
CAS号:743461-65-6
分子式: C40H42ClN5O7 分子量: 740.24
产品形式: Free Base
研发状态: Completed
研发用途: Pulmonary Disease Chronic Obstructive
研究机构: GlaxoSmithKline
研发日期: February 19 2014
研发阶段: Phase 1
Batefenterol (GSK961081, TD-5959) is both a muscarinic receptor antagonist and a β2-adrenoceptor agonist with Ki of 1.4 nM, 1.3 nM and 3.7 nM for hM2, hM3 muscarinic receptors and hβ2-adrenoceptor, respectively.
中文名称:吲哚美辛
CAS号:74252-25-8
分子式: C19H21ClNNaO7 分子量: 433.82
产品形式: sodium salt trihydrate
研发状态: Completed
研发用途: Pancreatitis; Cholangiopancreatography Endoscopic Retrograde; Indomethacin
研究机构: The First Affiliated Hospital of Soochow University
研发日期: November 1 2022
研发阶段: Not Applicable
Indometacin Sodium (Indomethacin Sodium) is the sodium salt of indomethacin, which is a non-selective, reversible, and competitive inhibitor of cyclooxygenases 1 and 2 with anti-inflammatory, analgesic-antipyretic and tocolytic effects.
中文名称:多沙唑嗪
CAS号:74191-85-8
分子式: C23H25N5O5 分子量: 451.48
产品形式: Free Base
研发状态: Completed
研发用途: Allergic Rhinitis
研究机构: University of Dundee
研发日期: Sep-13
研发阶段: Phase 4
Doxazosin(UK 33274) is a quinazoline-derivative that selectively antagonizes postsynaptic α1-adrenergic receptors.
中文名称:[4-氨基-2-[(1-甲磺酰基哌啶-4-基)氨基]嘧啶-5-基](2,3-二氟-6-甲氧基苯基)甲酮
CAS号:741713-40-6
分子式: C18H21F2N5O4S 分子量: 441.45
产品形式: free base
研发状态: Completed
研发用途: Neoplasms
研究机构: Hoffmann-La Roche
研发日期: May-05
研发阶段: Phase 1
R547 (Ro 4584820) is a potent ATP-competitive inhibitor of CDK1/2/4 with Ki of 2 nM/3 nM/1 nM. It is less potent to CDK7 and GSK3α/β, while inactive to other kinases. Phase 1.
中文名称:酮咯酸
CAS号:74103-06-3
分子式: C15H13N1O3 分子量: 255.27
产品形式: free base
研发状态: Recruiting
研发用途: Renal Colic; Flank Pain; Emergencies; Analgesia
研究机构: Hackensack Meridian Health
研发日期: December 21 2023
研发阶段: Phase 4
Ketorolac is a non-selective COX inhibitor of COX-1 and COX-2 with IC50 of 1.23 μM and 3.50 μM, respectively.
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