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PF-05105679

  Cat. No.:  DC21475   Featured
Chemical Structure
1398583-31-7
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More than 5000 active chemicals with high quality for research!
Field of application
PF-05105679 is a potent, selective TRPM8 channel inhibitor with IC50 of 103 nM (human TRPM8 currents inhibition).
Cas No.: 1398583-31-7
Chemical Name: PF 05105679
Synonyms: 3-[[[(1R)-1-(4-Fluorophenyl)ethyl](3-quinolinylcarbonyl)amino]methyl]-benzoic acid;PF05105679;[(R)-3-[(1-(4-fluorophenyl)ethyl)(quinolin-3-ylcarbonyl)amino]methylbenzoic acid;PF 05105679;DTXSID301336742;CS-0087256;3-((N-((1R)-1-(4-fluorophenyl)ethyl)-1-(quinolin-3-yl)formamido)methyl)benzoic acid;HY-115506;EX-A4888;SCHEMBL12487950;GTPL10300;3-[[[(1R)-1-(4-Fluorophenyl)ethyl](3-quinolinylcarbonyl)amino]methyl]benzoicacid;MS-27580;PF 5105679;AKOS030210975;UNII-F2B10OFV7Y;DA-56718;(R)-3-((N-(1-(4-fluorophenyl)ethyl)quinoline-3-carboxamido)methyl)benzoic acid;1398583-31-7;CHEMBL3577885;G14440;3-({N-[(1R)-1-(4-fluorophenyl)ethyl]-1-(quinolin-3-yl)formamido}methyl)benzoic acid;PF-05105679;BDBM50089245;3-[[[(1R)-1-(4-fluorophenyl)ethyl]-(quinoline-3-carbonyl)amino]methyl]benzoic acid;F2B10OFV7Y;YFC58331;3-((((1R)-1-(4-Fluorophenyl)ethyl)(3-quinolinylcarbonyl)amino)methyl)-benzoic acid;Benzoic acid, 3-((((1R)-1-(4-fluorophenyl)ethyl)(3-quinolinylcarbonyl)amino)methyl)-;DB15450;3-((((1R)-1-(4-fluorophenyl)ethyl)-(quinoline-3-carbonyl)amino)methyl)benzoic acid
SMILES: O=C(O)C1=CC=CC(CN([C@@H](C2=CC=C(F)C=C2)C)C(C3=CC4=CC=CC=C4N=C3)=O)=C1
Formula: C26H21N2O3F
M.Wt: 428.455
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: PF-05105679 is a potent, selective TRPM8 channel inhibitor with IC50 of 103 nM (human TRPM8 currents inhibition); displays >100-fold selectivity against a broad panel of 90 receptors, ion channels, and enzymes; demonstrates moderately potency against agonist (WS-12) and cold modalities of activation of TRPM8 in plate-based assay formats with IC50 of 181 and 480 nM, respectively, shows increased potency on voltage activation in HEK-293 cells at 12°C with IC50 of 13.8 nM; demonstrates activity in vivo in the guinea pig bladder ice water and menthol challenge tests with an IC50 of 200 nM and reduces core body temperature in the rats, and reduces pain in the cold pressor test in humans. Pain Phase 1 Clinical
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