硫酸奎尼丁结构式
|
常用名 | 硫酸奎尼丁 | 英文名 | Quinidine sulfate dihydrate |
---|---|---|---|---|
CAS号 | 6591-63-5 | 分子量 | 782.943 | |
密度 | N/A | 沸点 | 992.5ºC at 760 mmHg | |
分子式 | C20H24N2O2.1/2H2O4S.H2O | 熔点 | 212-214 °C (dec.)(lit.) | |
MSDS | 中文版 美版 | 闪点 | 554ºC | |
符号 |
GHS07 |
信号词 | Warning |
硫酸奎尼丁用途Quinidine sulfate dihydrate 是一种有效且选择性的细胞色素 P450db (cytochrome P450db) 抑制剂,可在体内抑制苯丙胺的代谢。Quinidine sulfate dihydrate 增强长春新碱 (VCR) 在肿瘤细胞中的细胞毒性,尤其是在 P388 白血病 (P388/VCR) 和人骨髓性白血病的VCR 耐药亚型中。 |
中文名 | 硫酸奎尼丁二水合物 |
---|---|
英文名 | Quinidine sulfate salt dihydrate |
中文别名 | 奎尼定硫酸盐 | 硫酸奎尼丁 | 硫酸奎尼丁 |
英文别名 | 更多 |
描述 | Quinidine sulfate dihydrate 是一种有效且选择性的细胞色素 P450db (cytochrome P450db) 抑制剂,可在体内抑制苯丙胺的代谢。Quinidine sulfate dihydrate 增强长春新碱 (VCR) 在肿瘤细胞中的细胞毒性,尤其是在 P388 白血病 (P388/VCR) 和人骨髓性白血病的VCR 耐药亚型中。 |
---|---|
相关类别 | |
靶点 |
IC50: cytochrome P450db; amphetamine metabolism[1] |
参考文献 |
沸点 | 992.5ºC at 760 mmHg |
---|---|
熔点 | 212-214 °C (dec.)(lit.) |
分子式 | C20H24N2O2.1/2H2O4S.H2O |
分子量 | 782.943 |
闪点 | 554ºC |
精确质量 | 782.356079 |
PSA | 192.62000 |
LogP | 6.52160 |
外观性状 | 固体 |
折射率 | 275 ° (C=2, 0.1mol/L HCl) |
储存条件 | 室温 |
Comparative study of the effects of antituberculosis drugs and antiretroviral drugs on cytochrome P450 3A4 and P-glycoprotein.
Antimicrob. Agents Chemother. 58(6) , 3168-76, (2014) Predicting drug-drug interactions (DDIs) related to cytochrome P450 (CYP), such as CYP3A4 and one of the major drug transporters, P-glycoprotein (P-gp), is crucial in the development of future chemoth... |
|
Diurnal variation in P-glycoprotein-mediated transport and cerebrospinal fluid turnover in the brain.
AAPS J. 16(5) , 1029-37, (2014) Nearly all bodily processes exhibit circadian rhythmicity. As a consequence, the pharmacokinetic and pharmacodynamic properties of a drug may also vary with time of day. The objective of this study wa... |
|
Effects of the inhibition of intestinal P-glycoprotein on aliskiren pharmacokinetics in cynomolgus monkeys.
Biopharm. Drug Dispos. 36(1) , 15-33, (2015) Aliskiren is a substrate for P-glycoprotein (P-gp) and is metabolized via cytochrome P450 3A4 (CYP3A4). The aim of the present study was to assess whether P-gp influenced the pharmacokinetics of alisk... |
Quinidine Sulfate Dihydrate |
Cinchonan-9-ol, 6'-methoxy-, (9S)-, sulfate, hydrate (2:1:2) (salt) |
EINECS 200-046-3 |
(9S)-6'-Methoxycinchonan-9-ol sulfate hydrate (2:1:2) |
MFCD00149346 |