前往化源商城

硫酸奎尼丁

更新时间:2024-01-02 13:57:49

硫酸奎尼丁结构式
硫酸奎尼丁结构式
品牌特惠专场
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
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。

 硫酸奎尼丁名称

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

 硫酸奎尼丁生物活性

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

[1]. David E. Moody, et al. Quinidine Inhibits In Vivo Metabolism of Amphetamine in Rats: Impact upon Correlation between GCIMS and Immunoassay Findings in Rat Urine. ournal of Analytical Toxicology, Vol. 14, September/October 1990

[2]. Tsuruo T, et al. Effects of quinidine and related compounds on cytotoxicity and cellular accumulation of vincristine and adriamycin in drug-resistant tumor cells.Cancer Res. 1984 Oct;44(10):4303-7.

 硫酸奎尼丁物理化学性质

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

 硫酸奎尼丁MSDS

 硫酸奎尼丁毒性和生态

 硫酸奎尼丁安全信息

符号 GHS07
GHS07
信号词 Warning
危害声明 H302
警示性声明 P301 + P312 + P330
个人防护装备 dust mask type N95 (US);Eyeshields;Gloves
危害码 (欧洲) Xn
风险声明 (欧洲) R22
安全声明 (欧洲) 13-36
危险品运输编码 NONH for all modes of transport
WGK德国 3
RTECS号 VA5605000

 硫酸奎尼丁文献8

更多文献
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...

 硫酸奎尼丁英文别名

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
品牌现货直购
推荐供应商:








查看所有供应商和价格请点击:

硫酸奎尼丁生产厂家

硫酸奎尼丁价格