化学性质:
规格 | 10mM (in 1mL DMSO) 10mg 50mg |
CAS | 1191252-49-9 |
别名 |
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化学名 | 3-(3,5-dibromo-4-oxocyclohexa-2,5-dien-1-ylidene)-N-[(4-phenoxyphenyl)methyl]-1,2,4-oxadiazole-5-carboxamide |
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 |
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].
特别提醒:
1. 本产品仅供科研使用。请勿用于医药、临床诊断或治疗,食品及化妆品等用途。请勿存放于普通住宅区。
2. 为了您的安全和健康,请穿好实验服并佩戴一次性手套和口罩操作。
标签:IOWH-032
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