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Efinaconazole

    
99.40%

Efinaconazole

源叶(MedMol)
S83806 一键复制产品信息
164650-44-6
C18H22F2N4O
348.3903
Efinaconazole [USAN:INN]; Efinaconazole (JAN/USAN/INN); EFINACONAZOLE; UNII-J82SB7FXWB; (2R,3R)-2-(2,4-difluorophenyl)-3-(4-methylidenepiperidin-1-yl)-1-(1,2,4-triazol-1-yl)butan-2-ol; KP-103; Efinaco
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S83806-5mg买3赠1
99.40%

¥382.00

>10 - - - -
S83806-10mg买3赠1
99.40%

¥552.00

>10 - - - -
S83806-50mg促销
99.40%

¥1530.00 ¥1220.00

>10 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: Efinaconazole (KP-103) 是14 alpha-demethylase的抑制剂。14 alpha-demethylase参与ergosterol的生物合成,ergosterol是真菌细胞膜的成分之一
靶点: 14 alpha-demethylase;Antifungal
体外研究: In in vitro antifungal susceptibility tests, efinaconazole shows lower minimum inhibitory concentration (MIC) than terbinafine, ciclopirox, itraconazole and amorolfine
体内研究: Efinaconazole is a topical antifungal, so it has relatively low systemic accumulation. The plasma half-life after 10 days of administration is 29.9 h. It has high plasma protein-binding affinity from 95.8 to 96.5%; primarily to albumin, a1-acid glycoprotein and γ-globulin. Efinaconazole is metabolized extensively through oxidative and reductive processes resulting in a sole H3 metabolite. It may also undergo glucuronidation. Efinaconazole does not have significant interactions with CYP450 enzymes in the liver. CYP2C8, CYP2C9, CYP2C19 and CYP3A4 are inhibited by efinaconazole at concentrations higher than the systemic concentrations achieved clinically
参考文献: 1. Gupta AK, et al. Efinaconazole (Jublia) for the treatment of onychomycosis. Expert Rev Anti Infect Ther. 2014, 12(7):743-52.
溶解性: Soluble  in  DMSO、Ethanol
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.87 ml 14.352 ml 28.703 ml
5 mM 0.574 ml 2.87 ml 5.741 ml
10 mM 0.287 ml 1.435 ml 2.87 ml
50 mM 0.057 ml 0.287 ml 0.574 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

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