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硫酸奎尼丁二水合物

硫酸奎尼丁二水合物

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?硫酸奎尼丁二水合物名称


















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




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硫酸奎尼丁




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硫酸奎尼丁



英文别名
更多





?硫酸奎尼丁二水合物生物活性




































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]


SMILES

O=S(O)(O)=O.[H]O[H].C=C[C@H]1C[N@](CC[C@H]1C2)[C@@]2(C)[C@@H](O)C3=CC=NC4=CC=C(OC)C=C34.[0.5]
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.







?硫酸奎尼丁二水合物物理化学性质
































沸点 992.5?C at 760 mmHg
熔点 212-214?°C (dec.)(lit.)
分子式 C20H24N2O2.1/2H2O4S.H2O
分子量 782.943
闪点 554?C
精确质量 782.356079
PSA 192.62000
LogP 6.52160
折射率 275 ° (C=2, 0.1mol/L HCl)






?硫酸奎尼丁二水合物MSDS







?硫酸奎尼丁二水合物毒性和生态




硫酸奎尼丁二水合物毒性英文版






?硫酸奎尼丁二水合物安全信息




































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














?硫酸奎尼丁二水合物文献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…









?硫酸奎尼丁二水合物英文别名
























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








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