Description
CFTRinh172 is a voltage-independent, selective CFTR chloride channel blocker that alters channel gating.
Product information
CAS Number: 307510-92-5
Molecular Weight: 409.40
Formula: C18H10F3NO3S2
Synonym:
CFTR Inhibitor-172
CFTR Inhibitor 172
CFTR Inhibitor172
CFTR(Inh)-172
CFTR(Inh) 172
CFTR(Inh)172
CFTR Inh-172
CFTR Inh 172
CFTR Inh172
Chemical Name: 4-{[(5Z)-4-Oxo-2-sulfanylidene-3-[3-(trifluoromethyl)phenyl]-1,3-thiazolidin-5-ylidene]methyl}benzoic acid
Smiles: OC(=O)C1C=CC(/C=C2\SC(=S)N(C3=CC(=CC=C3)C(F)(F)F)C\2=O)=CC=1
InChiKey: JIMHYXZZCWVCMI-ZSOIEALJSA-N
InChi: InChI=1S/C18H10F3NO3S2/c19-18(20,21)12-2-1-3-13(9-12)22-15(23)14(27-17(22)26)8-10-4-6-11(7-5-10)16(24)25/h1-9H,(H,24,25)/b14-8-
Technical Data
Appearance: Solid Power
Purity: ≥98% (or refer to the Certificate of Analysis)
Solubility: Soluble in DMSO
Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis
Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.
Shelf Life: ≥12 months if stored properly.
Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.
Drug Formulation: To be determined.
HS Tariff Code: 382200
How to use
In Vitro:
Inhibition by CFTRinh172 is complete in approximately 10 minutes (t1/2=4 minutes) and is reversed after ishout with t1/2 approximately 5 minutes. CFTRinh172 is nontoxic to FRT cells after 24 hours at concentrations up to 100 μM. CFTRinh172 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 Ki values for inhibition of Cl-current in wild-type, G551D, and G1349D CFTR are about 0.5 μM; however, Ki is significantly reduced to 0.2 μM for vF508 CFTR.
In Vivo:
A single intraperitoneal injection of CFTRinh172 (250 μg/kg) in mice reduces by more than 90% cholera toxin–induced fluid secretion in the small intestine over 6 hours. CFTRinh172 is nontoxic at high concentrations in mouse models. CFTRinh172 significantly reduces fluid secretion to that in saline control loops, whereas an inactive CFTRinh172 analog does not inhibit fluid secretion.
References:
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Products are for research use only. Not for human use.
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