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描述 | Ravuconazole displays a broad spectrum of antifungal activity against various fungi including Candida spp., Trichosporon beigelii, CNeoformans, and A. fumigatus. The MIC90 for these fungi ranges from 0.025 to 0.39 mg/mL. It demonstrates enhanced efficacy against strains of Candida krusei, with MICs from 0.05 to 0.39 mg/mL, and shows effective activity against T. mentagrophytes, T. rubrum, M. gypseum, and M. canis, with MICs from 0.05 to 0.39 mg/mL[1]. Ravuconazole is two to four times more potent than itraconazole and about 40 times more effective than fluconazole against yeasts. Both ravuconazole and itraconazole inhibit most aspergilli effectively, with cidal action against half of the isolates. They are also active against hyaline Hyphomycetes, dermatophytes, and dematiaceous fungi but inactive against Sporothrix schenckii and zygomycetes[2]. |
体内研究 | The peak concentration of ravuconazole in plasma and the area under the concentration-time curve exhibit good linearity across dosages ranging from 2 to 40 mg/kg. At a dose of 2.5 mg/kg, ravuconazole significantly delays mortality compared with control treatment and shows a considerable therapeutic effect against systemic cryptococcosis[1]. Ravuconazole significantly lowers CFU counts in the lungs compared to control levels. In a rat model of oral candidiasis, ravuconazole also significantly reduces CFU counts in oral swabs compared to controls, performing better than itraconazole and equally to fluconazole[3]. |
体外研究 | Ravuconazole displays a broad spectrum of antifungal activity against various fungi including Candida spp., Trichosporon beigelii, CNeoformans, and A. fumigatus. The MIC90 for these fungi ranges from 0.025 to 0.39 mg/mL. It demonstrates enhanced efficacy against strains of Candida krusei, with MICs from 0.05 to 0.39 mg/mL, and shows effective activity against T. mentagrophytes, T. rubrum, M. gypseum, and M. canis, with MICs from 0.05 to 0.39 mg/mL[1]. Ravuconazole is two to four times more potent than itraconazole and about 40 times more effective than fluconazole against yeasts. Both ravuconazole and itraconazole inhibit most aspergilli effectively, with cidal action against half of the isolates. They are also active against hyaline Hyphomycetes, dermatophytes, and dematiaceous fungi but inactive against Sporothrix schenckii and zygomycetes[2]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.29mL 0.46mL 0.23mL |
11.43mL 2.29mL 1.14mL |
22.86mL 4.57mL 2.29mL |
CAS号 | 182760-06-1 |
分子式 | C22H17F2N5OS |
分子量 | 437.47 |
SMILES Code | N#CC1=CC=C(C2=CSC([C@@H]([C@@](O)(C3=CC=C(F)C=C3F)CN4N=CN=C4)C)=N2)C=C1 |
MDL No. | MFCD00941002 |
别名 | 立福康唑 ;BMS-207147; ER-30346 |
运输 | 蓝冰 |
InChI Key | OPAHEYNNJWPQPX-RCDICMHDSA-N |
Pubchem ID | 467825 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Inert atmosphere, store in freezer, under -20°C |
溶解方案 |
DMSO: 50 mg/mL(114.29 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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