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Ravuconazole/雷夫康唑 {[allProObj[0].p_purity_real_show]}

货号:A573629

Ravuconazole是一种口服可用的三唑类抗真菌剂,可有效抑制多种真菌。

Ravuconazole/雷夫康唑 化学结构 CAS号:182760-06-1
Ravuconazole/雷夫康唑 化学结构
CAS号:182760-06-1
Ravuconazole/雷夫康唑 3D分子结构
CAS号:182760-06-1
Ravuconazole/雷夫康唑 化学结构 CAS号:182760-06-1
Ravuconazole/雷夫康唑 3D分子结构 CAS号:182760-06-1
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Ravuconazole/雷夫康唑 纯度/质量文件 产品仅供科研

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Ravuconazole/雷夫康唑 生物活性

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].

Ravuconazole/雷夫康唑 参考文献

[1]Hata K, et al. In vitro and in vivo antifungal activities of ER-30346, a novel oral triazole with a broad antifungal spectrumAntimicrob Agents Chemother. 1996 Oct;40(10):2237-42.

[2]Fung-Tomc JC, et al. In vitro activity of a new oral triazole, BMS-207147 (ER-30346)Antimicrob Agents Chemother. 1998 Feb;42(2):313-8.

[3]Hata K, et al. Efficacy of ER-30346, a novel oral triazole antifungal agent, in experimental models of aspergillosis, candidiasis, and cryptococcosisAntimicrob Agents Chemother. 1996 Oct;40(10):2243-7.

Ravuconazole/雷夫康唑 实验方案

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

Ravuconazole/雷夫康唑 技术信息

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

请根据您的动物给药指南选择适当的溶解方案。
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
方案一
方案二
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