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159668-20-9

中文名稱 奈沙加群
英文名稱 Napsagatran
CAS 159668-20-9
分子式 C26H34N6O6S
分子量 558.657
MOL 文件 159668-20-9.mol
159668-20-9 結(jié)構(gòu)式 159668-20-9 結(jié)構(gòu)式

基本信息

中文別名
奈沙加群
奈沙加群水合物
英文別名
Napsagatran
Ro 46-6240 hydrate
Napsagatran (hydrate)
Ro 46-6240/010 hydrate
Napsagatran [usan:inn]

物理化學(xué)性質(zhì)

儲存條件-20°C儲存
溶解度溶于二甲基亞砜

常見問題列表

生物活性
Napsagatran hydrate 是一種新型的特異性凝血酶 (thrombin) 抑制劑。
靶點

Thrombin

體外研究

Napsagatran (Ro 46-6240), the selective thrombin inhibitor, induces a dose-dependent prolongation of the activated partial thromboplastin time (aPTT) and prothrombin time (PT) that is evident 15 min after administration of the bolus of Napsagatran. Napsagatran also reduces the time to reperfusion in a dose-dependent manner and delays or prevents reocclusion. The decreasing intracellular amount and efflux of compound from the cells into the medium is measured. The measured CL int,efflux values are 0.13±0.06, 3.2±0.6, 10.1±2.3, and 110±2.8 for Digoxin, Fexofenadine, Napsagatran, and Rosuvastatin, respectively, thus representing drugs with a >800-fold range of efflux rates.

體內(nèi)研究

After the first hour of drug administration (from 0 to 60 min), the incorporated radioactivity into thrombi increased from baseline by 73±13, 67±22 and 32±10% in placebo, AP-1 and Napsagatran-treated rabbits, respectively. Statistical analysis confirm that thrombus growth in the placebo and AP-1 treated rabbits is not different. In contrast, reduction of 125 I-fibrinogen incorporation by Napsagatran is statistical different from the placebo group (P<0.01).

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