溶解性 | Soluble in water (0.05 mg/ml at 25 °C), methanol (50 mg/ml), ethanol (9 mg/ml at 25 °C), DMSO (71 mg/ml at 25 °C), and DMF (~ 30 mg/ml). |
应用 | Treatment of human colorectal cancer cell lines induces MRP1 and MRP3 but not other members of the MRP family. Reported to significantly increase the cytotoxicity of the anthracyclines (doxorubicin, daunorubicin and epirubicin), as well as teniposide, VP- |
产品介绍 | Sulindac 是一种非甾体抗炎剂。 |
备注 | Sulindac (Clinoril) is a non-steroidal anti-inflammatory agent of the arylalkanoic acid class. |
生化机理 | Sulindac inhibits the NF-κB pathway. Sulindac is a non-steroidal anti-inflammatory drug. Sulindac reduces the level and activity of several cyclin-dependent kinases (CDKs) and induces apoptosis. Sulindac metabolizes to sulindac sulfide, a Cox (cyclooxygenase) inhibitor that represses ras signaling, and sulindac sulfone, an antitumor agent. Sulindac is an inhibitor of Cox-1 and Cox-2. |
别名 | 舒林酸; (Z)-5-氟-2-甲基-1-[4-(甲亚硫酰苯基)亚甲基]-1H-茚-3-醋酸;Aflodac; Sulinol; Sulreuma;MK-231;(Z)-5-Fluoro-2-methyl-1-[[4-(methylsulfinyl)phenyl]methylene]-1H-indene-3-acetic acid; cis-5-Fluoro-2-methyl-1-[p-(methylsulfinyl)benzylidene]-indene-3-acetic acid |