CAS NO: | 61618-27-7 |
生物活性 | Amfenac Sodium Hydrate is aCOX-2inhibitor. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | Cells transfected to express COX-2 have a higher proliferation rate than those do not. The addition of Amfenac Sodium Hydrate significantly decreases the proliferation rate of all cell lines. Nitric oxide production by macrophages is inhibited by the addition of melanoma conditioned medium, the addition of Amfenac Sodium Hydrate partially overcomes this inhibition[1]. Results show that Amfenac Sodium Hydrate inhibits the release of B-glucuronidase: 5×10-4M Amfenac Sodium Hydrate inhibits the release of the enzyme 35.3 and 16.3% in the presence of 10-8, and 10-7M FMLP, respectively. Addition of 10-4M Amfenac Sodium Hydrate causes 28.3% inhibition of aggregation of polgmorphonuclear leukocgtes (PMNs) during incubation for 16 min with 10-8M FMLP[2]. | ||||||||||||||||
分子量 | 295.27 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C15H14NNaO4 | ||||||||||||||||
CAS 号 | 61618-27-7 | ||||||||||||||||
中文名称 | 氨芬酸钠水合物 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 150 mg/mL(508.01 mM;Need ultrasonic and warming) H2O : 50 mg/mL(169.34 mM;Need ultrasonic) 配制储备液
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