CAS NO: | 1334546-77-8 |
生物活性 | Icenticaftor (QBW251) is an orally activeCFTRchannel potentiator, withEC50s of 79 nM and 497 nM forF508delandG551DCFTR, respectively. Icenticaftor can be used for chronic obstructive pulmonary disease (COPD) and cystic fibrosis research[1]. | ||||||||||||||||
IC50& Target | EC50: 79 nM (F508del CFTR) and 497 nM (G551D CFTR)[1] | ||||||||||||||||
体外研究 (In Vitro) | Icenticaftor (QBW251), an orally bioavailable small molecule CFTR potentiator, can restore CFTR function in specific CFTR genotypes as well as wild-type CFTR[2]. | ||||||||||||||||
体内研究 (In Vivo) | In Sprague-Dawley rats, the pharmacokinetic profile of Icenticaftor is established. After oral administration at a dose of 3 mg/kg, the oral bioavailability is 90%, and AUClastis 20 635 nmol/Loh[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 361.24 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C12H13F6N3O3 | ||||||||||||||||
CAS 号 | 1334546-77-8 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 150 mg/mL(415.24 mM;ultrasonic and warming and heat to 60℃) 配制储备液
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以下溶剂前显示的百
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