伊曲康唑
基本信息
| 产品名称 |
伊曲康唑 |
| 英文名称 |
Itraconazole |
| 别名 |
伊曲康唑;4-[4-[4-[4-[[2-(2,4-二氯苯基)-2-(1H-1,2,4-三唑-1-基甲基)-1,3-二氧戊环-4-基]甲氧基]苯基]-1-哌嗪基]苯基]-2,4-二氢-2-(1-甲基丙基)-3H-1,2,4-三唑-3-酮;斯皮仁诺;依他康唑;亚特那唑;奥立康唑;孢粉; R51211 |
| 英文别名 |
Oriconazole;R51211;Sporanox;2-butan-2-yl-4-[4-[4-[4-[[(2R,4S)-2-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazin-1-yl]phenyl]-1,2,4-triazol-3-one |
| 规格或纯度 |
2mM in DMSO |
| 运输条件 |
超低温冰袋运输 |
| 生化机理 |
细胞色素p450 CYP3A4抑制剂(咪达唑仑羟基化的IC 50 = 16-26 nM)。对真菌酶的亲和力高于哺乳动物细胞色素p450。穿越血脑屏障的能力有限。抗真菌活性。 |
一般描述
Itraconazole is a triazole antifungal agent. It inhibits the fungal CYP(cytochrome P450) oxidase-mediated synthesis of ergosterol. Itraconazole also acts as an effective hedgehog signaling inhibitor in a Ptch-independent manner, presumably by binding smoothened (Smo) at a site distinct from that targeted by cyclopamine and SAG. Itraconazole is an inhibitor of CYP3A4.
Itraconazole is a triazole antifungal agent. It inhibits the fungal CYP(cytochrome P450) oxidase-mediated synthesis of ergosterol. Itraconazole also acts as an effective hedgehog signaling inhibitor in a Ptch-independent manner, presumably by binding smoothened (Smo) at a site distinct from that targeted by cyclopamine and SAG. Itraconazole is an inhibitor of CYP3A4.
A traizole antifungal agent
相关属性
| CAS编号 |
84625-61-6 |
| 敏感性 |
对热敏感 |
| 熔点 |
167.0 to 171.0 °C |
| 储存温度 |
-80℃储存 |
| Reaxys-RN |
6042047 |
| RTECS |
XZ5481000 |
| 分子量 |
705.63 |
| 分子式 |
C35H38Cl2N8O4 |
| 品牌 |
Jinpan |
| PubChem CID |
3793 |