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182760-06-1

中文名称 立福康唑
英文名称 4-[2-[(2R,3R)-3-(2,4-difluorophenyl)-3-hydroxy-4-(1,2,4-triazol-1-yl)b utan-2-yl]-1,3-thiazol-4-yl]benzonitrile
CAS 182760-06-1
分子式 C22H17F2N5OS
分子量 437.47
MOL 文件 182760-06-1.mol
更新日期 2024/05/26 16:05:22
182760-06-1 结构式 182760-06-1 结构式

基本信息

中文别名
雷氟康唑
里氟康唑
立福康唑
立福康唑,雷夫康唑
立福康唑/雷夫康唑/立福康唑/BMS 207147
英文别名
Rcz
Er-30346
Aids057176
Bms-207147
Bms-207,147
Aids-057176
BMS-207147/Ravuconazole
Ravuconazole, BMS-207147
4-[2-[(2R,3R)-3-(2,4-difluorophenyl)-3-hydroxy-4-(1,2,4-triazol-1-yl)b utan-2-yl]-1,3-thiazol-4-yl]benzonitrile
Benzonitrile, 4-[2-[(1R,2R)-2-(2,4-difluorophenyl)-2-hydroxy-1-methyl-3-(1H-1,2,4-triazol-1-yl)propyl]-4-thiazolyl]-

物理化学性质

熔点64-66°C
比旋光度D24 -29.1° (c = 1.03 in methanol)
沸点674.9±65.0 °C(Predicted)
密度1.38±0.1 g/cm3(Predicted)
储存条件-20°C冷冻
溶解度DMF: 25 mg/ml; DMF:PBS (pH 7.2) (1:4): 0.25 mg/ml; DMSO: 20 mg/ml; Ethanol: 5 mg/ml
酸度系数(pKa)11.62±0.29(Predicted)
形态结晶固体

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H315-H319-H335
立福康唑价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30HY-14272立福康唑
Ravuconazole
182760-06-12 mg400元
2024/04/30HY-14272立福康唑
Ravuconazole
182760-06-15 mg600元
2024/04/30HY-14272立福康唑
Ravuconazole
182760-06-110 mg900元

常见问题列表

生物活性
Ravuconazole (BMS-207147;ER-30346) 是一种口服的三唑抗真菌药物,能够有效广谱的抑制真菌。
靶点

Fungal

体外研究

Ravuconazole shows a broad spectrum of activity against a wide range of fungi covering Candida spp. , Trichosporon beigelii , C. neoformans and A. fumigatus . The MIC 90 ranges from 0.025 to 0.39 mg/mL.Ravuconazoleshows relatively higher levels of activity against three strains of Candida krusei , with MICs ranging from 0.05 to 0.39 mg/mL.Ravuconazoleshows good activity against T. mentagrophytes , T. rubrum , M. gypseum and M. canis with MICs ranging from 0.05 to 0.39 mg/mL. Ravuconazoleis about two- to four fold more potent than itraconazole and about 40-fold more active than fluconazole against yeasts. Ravuconazoleand itraconazoleare inhibitory to most aspergilli, and against half of the isolates, the activity iscidal. Ravuconazoleand itraconazoleare active, though not cidal, against most hyaline Hyphomycetes , dermatophytes, and the dematiaceous fungi and inactive against Sporothrix schenckii and zygomycetes.

体内研究

The maximum concentration of ravuconazole in plasma and the area under the concentration-time curve for ravuconazoleshow good linearity over a range of doses from 2 to 40 mg/kg of body weight. Ravuconazole at a dose of 2.5 mg/kg delays mortality significantly compared with the control treatment.Ravuconazole also shows a substantial therapeutic effect against systemic cryptococcosis. Ravuconazole reduces the numbers of CFU in the lungs significantly compared with the numbers of CFU in the lungs of the controls. In an experimental model of oral candidiasis in rats, ravuconazole reduces the numbers of CFU in oral swabs significantly compared with the numbers of CFU in oral swabs from the controls and is more effective than itraconazole and as effective as fluconazole..

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