CAS NO: | 307510-92-5 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 |
CFTR(inh)-172 is a potent and selective blocker of theCFTRchloride channel; reversibly inhibitsCFTRshort-circuit current in less than 2 minutes with aKiof 300 nM. |
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IC50& Target |
Ki: 300 nM (CFTR)[1] |
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体外研究 (In Vitro) |
Inhibition by CFTR(inh)-172 is complete in approximately 10 minutes (t1/2=4 minutes) and is reversed after ishout with t1/2approximately 5 minutes. CFTRinh-172 is nontoxic to FRT cells after 24 hours at concentrations up to 100 μM[1]. CFTR(inh)-172 does not alter CFTR unitary conductance (8 pS), but reduces open probability by >90% with Ki=0.6 μM. This effect is due to increased mean channel closed time without changing mean channel open time. The Kivalues for inhibition of Cl-current in wild-type, G551D, and G1349D CFTR are about 0.5 μM; however, Kiis significantly reduced to 0.2 μM for vF508 CFTR[2].
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体内研究 (In Vivo) |
A single intraperitoneal injection of CFTR(inh)-172 (250 μg/kg) in mice reduces by more than 90% cholera toxin–induced fluid secretion in the small intestine over 6 hours. CFTR(inh)-172 is nontoxic at high concentrations in mouse models. CFTRinh-172 significantly reduces fluid secretion to that in saline control loops, whereas an inactive CFTRinh-172 analog does not inhibit fluid secretion[1].
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分子量 |
409.40 |
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性状 |
Solid |
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Formula |
C18H10F3NO3S2 |
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CAS 号 |
307510-92-5 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 50 mg/mL(122.13 mM;Need ultrasonic)
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In Vivo:
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