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产品名称 | CFTR ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Ataluren | ✔ | 98% | |||||||||||||||||
Lumacaftor |
++++
F508del-CFTR, EC50: 0.1 μM |
98% | |||||||||||||||||
CFTR(inh)-172 |
+++
CFTR, Ki: 300 nM |
99%+ | |||||||||||||||||
GlyH-101 |
+
CFTR, Ki: 4.3 μM |
99%+ | |||||||||||||||||
IOWH-032 |
++
CFTR, IC50: 1.01 μM |
99%+ | |||||||||||||||||
Tezacaftor | ✔ | 99%+ | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | Icenticaftor, also known as QBW251, is an orally active CFTR channel potentiator with EC50 values of 79 nM and 497 nM for F508del CFTR and G551D CFTR, respectively.Icenticaftor is used in chronic obstructive pulmonary disease (COPD) and cystic fibrosis studies[1].Icenticaftor is an orally bioactive small molecule CFTR potentiator that restores the function of specific mutant and wild-type CFTRs[2]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.77mL 0.55mL 0.28mL |
13.84mL 2.77mL 1.38mL |
27.68mL 5.54mL 2.77mL |
CAS号 | 1334546-77-8 |
分子式 | C12H13F6N3O3 |
分子量 | 361.24 |
SMILES Code | O=C(C1=NC(OC)=C(C(F)(F)F)C=C1N)NC[C@](C)(O)C(F)(F)F |
MDL No. | MFCD31631074 |
别名 | QBW251; NVP-QBW251 |
运输 | 蓝冰 |
InChI Key | USHQRIKZLHNPQR-JTQLQIEISA-N |
Pubchem ID | 58442344 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Keep in dark place, sealed in dry, 2-8°C |