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112559-91-8

中文名称 羟基伊曲康唑(伊曲康唑代谢物)
英文名称 HYDROXY ITRACONAZOLE
CAS 112559-91-8
分子式 C35H40Cl2N8O4
分子量 707.65
MOL 文件 112559-91-8.mol
更新日期 2024/05/20 09:19:54
112559-91-8 结构式 112559-91-8 结构式

基本信息

中文别名
羟基伊曲康唑
伊曲康唑杂质1
伊曲康唑代谢物
伊曲康唑2-羟基代谢物
羟基伊曲康唑(伊曲康唑代谢物)
英文别名
R 63373
HYDROXY ITRACONAZOLE
Itraconazole Impurity 1
Itraconazole 2-Hydroxy Metabolite
Itraconazole metabolite Hydroxy Itraconazole
4-[4-[4-[4-[[2-(2,4-Dichlorophenyl)-2-(1H-1,2,4-triazol-1-ylMethyl)-1,3-dioxolan-4-yl]Methoxy]phenyl]-1-piperazinyl]phenyl]-2,4-dihydro-2-(2-hydroxy-1-Methylpropyl)-
3H-1,2,4-Triazol-3-one, 4-4-4-4-2-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-ylmethoxyphenyl-1-piperazinylphenyl-2,4-dihydro-2-(2-hydroxy-1-methylpropyl)-
4-[4-[4-[4-[[2-(2,4-Dichlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]-1-piperazinyl]phenyl]-2,4-dihydro-2-(2-hydroxy-1-methylpropyl)-3H-1,2,4-triazol-3-one
所属类别
分析化学:药典标准品和杂质标准品

物理化学性质

熔点76-78°C
沸点884.7±75.0 °C(Predicted)
密度1.44±0.1 g/cm3(Predicted)
储存条件-20°C冷冻
溶解度可溶于氯仿(少许)、乙酸乙酯(少许)、甲醇(少许)
酸度系数(pKa)14.72±0.20(Predicted)
形态固体
颜色白色至浅米色
羟基伊曲康唑(伊曲康唑代谢物)价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/08/19HY-12772羟基伊曲康唑(伊曲康唑代谢物)
Hydroxy Itraconazole
112559-91-81mg1900元
2024/08/19HY-12772羟基伊曲康唑(伊曲康唑代谢物)
Hydroxy Itraconazole
112559-91-85mg7500元
2023/10/26HY-12772羟基伊曲康唑(伊曲康唑代谢物)
Hydroxy Itraconazole
112559-91-810mg12000元

常见问题列表

生物活性
Hydroxy Itraconazole (Itraconazole metabolite Hydroxy Itraconazole; R-63373) 是 Itraconazole (ITZ) 的活性代谢物,Itraconazole 是一种三唑类抗真菌剂。
靶点

Antifungal

体外研究

Hydroxy Itraconazole (Itraconazole metabolite Hydroxy Itraconazole; R-63373) is an active metabolite of Itraconazole (ITZ). Although Hydroxy Itraconazole is also reported to have antifungal activity in vitro, its pharmacokinetics in humans has been studied less than that of ITZ. ITZ and Hydroxy Itraconazole have a triazole ring and inhibit CYP3A. Their half-lives can be extended by 26-60% with repeated administration compared to single administration.

体内研究

The plasma concentration of Hydroxy Itraconazole is weakly dependent on the dose of ITZ, most likely because the process that forms Hydroxy Itraconazole is saturated. Serum albumin and GFR may alter the pharmacokinetics of ITZ and Hydroxy Itraconazole. Antifungal activity should be discussed while taking into account not only the plasma concentration of ITZ but also that of Hydroxy Itraconazole. However, the pharmacokinetics of Hydroxy Itraconazole is similar to that of ITZ in immunocompromised patients taking an oral solution of ITZ. Since the plasma concentrations of ITZ and Hydroxy Itraconazole are closely correlated, determining the plasma concentration of either should be sufficient from a clinical point of view.

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