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1467059-66-0

1467059-66-0 Structure

1467059-66-0 Structure
IdentificationBack Directory
[Name]

(S)-4,6-difluoro-5-(4-(tetrahydro-2H-pyran-2-yl)phenyl)-1H-indole-3-carboxylic acid
[CAS]

1467059-66-0
[Synonyms]

PF6679142
PF-6679142
PF 6679142
PF-06679142
(S)-4,6-difluoro-5-(4-(tetrahydro-2H-pyran-2-yl)phenyl)-1H-indole-3-carboxylic acid
1H-Indole-3-carboxylic acid, 4,6-difluoro-5-[4-[(2S)-tetrahydro-2H-pyran-2-yl]phenyl]-
[Molecular Formula]

C20 H17 F2 N O3
[MOL File]

1467059-66-0.mol
[Molecular Weight]

357.35
Chemical PropertiesBack Directory
[Boiling point ]

573.1±50.0 °C(Predicted)
[density ]

1.372±0.06 g/cm3(Predicted)
[pka]

2.00±0.30(Predicted)
[InChI]

InChI=1S/C20H17F2NO3/c21-14-9-15-18(13(10-23-15)20(24)25)19(22)17(14)12-6-4-11(5-7-12)16-3-1-2-8-26-16/h4-7,9-10,16,23H,1-3,8H2,(H,24,25)/t16-/m0/s1
[InChIKey]

JQJNGAWEMYQJIQ-INIZCTEOSA-N
[SMILES]

N1C2=C(C(F)=C(C3=CC=C([C@H]4OCCCC4)C=C3)C(F)=C2)C(C(O)=O)=C1
Hazard InformationBack Directory
[Uses]

PF-06679142 (Compound 10) is a potent, orally active AMPK activator with an EC50 of 22 nM against α1β1γ1-AMPK. PF-06679142 can be used for diabetic nephropathy research[1].
[IC 50]

AMPK α1β1γ1: 22 nM (EC50)
[References]

[1] Edmonds DJ, et al. Optimization of Metabolic and Renal Clearance in a Series of Indole Acid Direct Activators of 5'-Adenosine Monophosphate-Activated Protein Kinase (AMPK). J Med Chem. 2018 Mar 22;61(6):2372-2383. DOI:10.1021/acs.jmedchem.7b01641
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