CAS NO: | 849675-87-2 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Encequidar mesylate (HM30181 mesylate; HM30181A mesylate) is a competitive and potentP-glycoproteininhibitor. | ||||||||||||||||
IC50& Target | P-glycoprotein[1][2]. | ||||||||||||||||
体外研究 (In Vitro) | Treatment of 0.1 or 1 nM Encequidar (HM30181) lead to 20 and 42% inhibition of survival at the 100 nM and 1000 nM NSC 125973 treatment, respectively[2]. | ||||||||||||||||
体内研究 (In Vivo) | The plasma concentrations of Encequidar (HM30181) are higher for the simultaneous administration with the microcapsule than with the powder; providing significant differences from 1 to 2 h. The microcapsule has about a 1.7-fold faster Tmaxand a 1.6-fold higher AUC value compared with the powder (2.5±0.6 vs. 4.3±0.9 h; 107.7±20.1 vs. 64.3±18.0 h ng/mL). The faster and overall improved absorption of Encequidar (HM30181) in microcapsule form might be due to the remarkable enhancement of the aqueous solubility and dissolution resulting from its crystalline conversion to the amorphous form and particle size reduction[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 784.83 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C39H40N6O10S | ||||||||||||||||
CAS 号 | 849675-87-2 | ||||||||||||||||
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 : 25 mg/mL(31.85 mM;Need ultrasonic) 配制储备液
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