
中文名称:盐酸普鲁卡因
CAS号:51-05-8
分子式: C13H20N2O2.HCl 分子量: 272.77
产品形式: HCl
研发状态: Completed
研发用途: Spinal Anesthesia
研究机构: University Hospital Ghent
研发日期: September 16 2015
研发阶段: Phase 4
Procaine (Novocaine) is an inhibitor of sodium channel, NMDA receptor and nAChR with IC50 of 60 μM, 0.296 mM and 45.5 μM, which is also an inhibitor of 5-HT3 with KD of 1.7 μM.
中文名称: 氟比洛芬
CAS号:5104-49-4
分子式: C15H13FO2 分子量: 244.26
产品形式: free base
研发状态: Not yet recruiting
研发用途: Lidocaine; Analgesia; Pain Postoperative; Thoracic Surgery
研究机构: Qilu Hospital of Shandong University
研发日期: Jun-23
研发阶段: Not Applicable
Flurbiprofen is a member of the phenylalkanoic acid derivative family of non-steroidal anti-inflammatory drugs (NSAIDs).
中文名称: 阿西莫司
CAS号:51037-30-0
分子式: C6H6N2O3 分子量: 154.12
产品形式: free base
研发状态: Recruiting
研发用途: Pre Diabetes
研究机构: Maastricht University Medical Center
研发日期: February 20 2024
研发阶段: --
Acipimox (Olbemox,K-9321) is a niacin derivative used as a hypolipidemic agent.
中文名称:硫酸沙丁胺醇
CAS号:51022-70-9
分子式: C13H21NO3.H2SO4 分子量: 337.39
产品形式: Sulfate
研发状态: Recruiting
研发用途: Asthma
研究机构: Teva Branded Pharmaceutical Products R&D Inc.
研发日期: May 2 2024
研发阶段: Phase 1
Salbutamol Sulfate (Albuterol, Ventolin, Aerolin, Ventorlin, Asthalin, Asthavent) is a short-acting β2-adrenergic receptor agonist with an IC50 of 8.93 µM.
中文名称:D(+)-无水葡萄糖
CAS号:50-99-7
分子式: C6H12O6 分子量: 180.16
产品形式: free base
研发状态: Not yet recruiting
研发用途: Pregnancy in Diabetic; Diabetes Mellitus Type 1
研究机构: Turku University Hospital
研发日期: June 1 2024
研发阶段: --
Dextrose (D-glucose), a simple sugar (monosaccharide), is an important carbohydrate in biology.
中文名称:5-氟-2'-脱氧脲核苷
CAS号:50-91-9
分子式: C9H11FN2O5 分子量: 246.19
产品形式: free base
研发状态: Completed
研发用途: Unresectable Colorectal Liver Metastases
研究机构: David Bartlett; The Pittsburgh Foundation; Sanofi; University of Pittsburgh
研发日期: May-03
研发阶段: Phase 1
Floxuridine (NSC 27640, Deoxyfluorouridine, FUDR) is a prodrug that is rapidly catabolized to 5-fluorouracil in vivo. Floxuridine is used to treat various cancers, particularly metastases to the liver. Floxuridine inhibits Poly(ADP-Ribose) polymerase and induces DNA damage and apoptosis. Floxuridine has antiviral effects against HSV and CMV.
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