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182760-06-1

中文名稱 立福康唑
英文名稱 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 2025/01/10 21:55:35
182760-06-1 結(jié)構(gòu)式 182760-06-1 結(jié)構(gòu)式

基本信息

中文別名
雷氟康唑
里氟康唑
立??颠?BR>立??颠?雷夫康唑
立??颠?雷夫康唑/立??颠?BMS 207147
英文別名
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]-

物理化學(xué)性質(zhì)

熔點(diǎn)64-66°C
比旋光度D24 -29.1° (c = 1.03 in methanol)
沸點(diǎn)674.9±65.0 °C(Predicted)
密度1.38±0.1 g/cm3(Predicted)
儲存條件-20°C冷凍
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
酸度系數(shù)(pKa)11.62±0.29(Predicted)
形態(tài)結(jié)晶固體
顏色Off-white to yellow

安全數(shù)據(jù)

危險(xiǎn)性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H315-H319-H335
立??颠騼r(jià)格(試劑級)
報(bào)價(jià)日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價(jià)格
2024/11/08HY-14272立福康唑
Ravuconazole
182760-06-12 mg400元
2024/11/08HY-14272立??颠?BR>Ravuconazole182760-06-15 mg600元
2024/11/08HY-14272立??颠?BR>Ravuconazole182760-06-110 mM * 1 mLin DMSO660元

常見問題列表

生物活性
Ravuconazole (BMS-207147;ER-30346) 是一種口服的三唑抗真菌藥物,能夠有效廣譜的抑制真菌。
靶點(diǎn)

Fungal

體外研究

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.

體內(nèi)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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