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898562-94-2

898562-94-2 | Quinoline, 2-[[4-[1-methyl-4-(4-pyridinyl)-1H-pyrazol-3-yl]phenoxy]methyl]-

CAS No: 898562-94-2 Catalog No: AG00H0HG MDL No:MFCD09743765

Product Description

Catalog Number:
AG00H0HG
Chemical Name:
Quinoline, 2-[[4-[1-methyl-4-(4-pyridinyl)-1H-pyrazol-3-yl]phenoxy]methyl]-
CAS Number:
898562-94-2
MDL Number:
MFCD09743765
IUPAC Name:
2-[[4-(1-methyl-4-pyridin-4-ylpyrazol-3-yl)phenoxy]methyl]quinoline
InChI:
InChI=1S/C25H20N4O/c1-29-16-23(18-12-14-26-15-13-18)25(28-29)20-7-10-22(11-8-20)30-17-21-9-6-19-4-2-3-5-24(19)27-21/h2-16H,17H2,1H3
InChI Key:
AZEXWHKOMMASPA-UHFFFAOYSA-N
UNII:
R9Y8EY0G42

Properties

Complexity:
531  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
392.164g/mol
Formal Charge:
0
Heavy Atom Count:
30  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
392.462g/mol
Monoisotopic Mass:
392.164g/mol
Rotatable Bond Count:
5  
Topological Polar Surface Area:
52.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.2  

Literature

Title Journal
Phosphodiesterase 10A Inhibition Improves Cortico-Basal Ganglia Function in Huntington's Disease Models. Neuron 20161221
A novel thermoregulatory role for PDE10A in mouse and human adipocytes. EMBO molecular medicine 20160701
Phosphodiesterase 2 inhibitors promote axonal outgrowth in organotypic slice co-cultures. Neuro-Signals 20130101
Rapid identification of a novel small molecule phosphodiesterase 10A (PDE10A) tracer. Journal of medicinal chemistry 20120524
Synthesis and in vitro evaluation of new analogues as inhibitors for phosphodiesterase 10A. European journal of medicinal chemistry 20110901
Synthesis, in vivo occupancy, and radiolabeling of potent phosphodiesterase subtype-10 inhibitors as candidates for positron emission tomography imaging. Journal of medicinal chemistry 20110825
Radiosynthesis and in vivo evaluation of [(11)C]MP-10 as a positron emission tomography radioligand for phosphodiesterase 10A. Nuclear medicine and biology 20110801
Triazoloquinazolines as a novel class of phosphodiesterase 10A (PDE10A) inhibitors. Bioorganic & medicinal chemistry letters 20110615
Radiosynthesis and in vivo evaluation of [11C]MP-10 as a PET probe for imaging PDE10A in rodent and non-human primate brain. Bioorganic & medicinal chemistry 20110301
The atypical anxiolytic drug, tofisopam, selectively blocks phosphodiesterase isoenzymes and is active in the mouse model of negative symptoms of psychosis. Journal of neural transmission (Vienna, Austria : 1996) 20101101
Effects of phosphodiesterase 10 inhibition on striatal cyclic AMP and peripheral physiology in rats. Acta neurobiologiae experimentalis 20100101
Inhibition of the striatal specific phosphodiesterase PDE10A ameliorates striatal and cortical pathology in R6/2 mouse model of Huntington's disease. PloS one 20100101
Phosphodiesterase 10A inhibitor activity in preclinical models of the positive, cognitive, and negative symptoms of schizophrenia. The Journal of pharmacology and experimental therapeutics 20091101
Discovery of a novel class of phosphodiesterase 10A inhibitors and identification of clinical candidate 2-[4-(1-methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl]-quinoline (PF-2545920) for the treatment of schizophrenia. Journal of medicinal chemistry 20090827
Preclinical characterization of selective phosphodiesterase 10A inhibitors: a new therapeutic approach to the treatment of schizophrenia. The Journal of pharmacology and experimental therapeutics 20080501

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