CAS NO: | 1191252-49-9 |
包装 | 价格(元) |
10mM (in 1mL DMSO) | 电议 |
10mg | 电议 |
50mg | 电议 |
Cas No. | 1191252-49-9 |
别名 | 3-(3,5-二溴-4-羟基苯基)-N-(4-苯氧基苄基)-1,2,4-恶二唑-5-甲酰胺 |
化学名 | 3-(3,5-dibromo-4-oxocyclohexa-2,5-dien-1-ylidene)-N-[(4-phenoxyphenyl)methyl]-1,2,4-oxadiazole-5-carboxamide |
Canonical SMILES | C1=CC=C(C=C1)OC2=CC=C(C=C2)CNC(=O)C3=NC(=C4C=C(C(=O)C(=C4)Br)Br)NO3 |
分子式 | C22H15Br2N3O4 |
分子量 | 545.18 |
溶解度 | ≥ 21.85mg/mL in DMSO |
储存条件 | Store at -20°C |
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. |
Shipping Condition | Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request |
产品描述 | Target: CFTR IC50: 1.01 μM IOWH-032 is a potent and synthetic extracellular cystic fibrosis transmembrane conductance regulator (CFTR) inhibitor with IC50 value of 1.01 μM in T84 and CHO-CFTR cell based assays [1]. The CFTR chloride channel is the most attractive because it is the primary driver of secretion in cases of diarrhea caused by enterotoxigenic bacteria. CFTR plays an important role in transepithelial fluid homeostasis through controlling the flow of chloride ions and thus the movement of water in and out of cells [1]. In vitro: IOWH032 inhibited CFTR activity with IC50 value of 6.87 μM in T84-CFTR cell based assays [1]. IOWH-032 rapidly blocked and potentiated hCFTR activity in a concentration-dependent manner with apparent Kd value of 6.1 nM and 0.64 nM, respectively. However, IOWH-032 did not potentiate and only blocked mCFTR with an apparent Kd value of 42.9 μM [2]. In vivo: IOWH032 significantly inhibited cholera toxin (CTX)-induced secretion in a mouse closed-loop model. Moreover, IOWH032 (5 mg/kg, po dose) decreased the fecal output index by apparent 70% compared to vehicle (cholera toxin) in a cecetomized rat model. IOWH032 inhibited CFTR activity with IC50 value of 6.87 μM in T84-CFTR cell based assays [1]. References: |