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2-((1-Cyclopentyl-1H-pyrazol-4-yl)oxy)pyrido[3,4-d]-pyrimidin-4(3H)-one ID: ALA3769724
Chembl Id: CHEMBL3769724
PubChem CID: 136053680
Max Phase: Preclinical
Molecular Formula: C15H15N5O2
Molecular Weight: 297.32
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: O=c1[nH]c(Oc2cnn(C3CCCC3)c2)nc2cnccc12
Standard InChI: InChI=1S/C15H15N5O2/c21-14-12-5-6-16-8-13(12)18-15(19-14)22-11-7-17-20(9-11)10-3-1-2-4-10/h5-10H,1-4H2,(H,18,19,21)
Standard InChI Key: ARDXICZNEUJDDE-UHFFFAOYSA-N
Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 297.32Molecular Weight (Monoisotopic): 297.1226AlogP: 2.42#Rotatable Bonds: 3Polar Surface Area: 85.69Molecular Species: NEUTRALHBA: 6HBD: 1#RO5 Violations: ┄HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): ┄CX Acidic pKa: 8.00CX Basic pKa: 2.40CX LogP: 1.62CX LogD: 1.53Aromatic Rings: 3Heavy Atoms: 22QED Weighted: 0.80Np Likeness Score: -0.72
References 1. Westaway SM, Preston AG, Barker MD, Brown F, Brown JA, Campbell M, Chung CW, Drewes G, Eagle R, Garton N, Gordon L, Haslam C, Hayhow TG, Humphreys PG, Joberty G, Katso R, Kruidenier L, Leveridge M, Pemberton M, Rioja I, Seal GA, Shipley T, Singh O, Suckling CJ, Taylor J, Thomas P, Wilson DM, Lee K, Prinjha RK.. (2016) Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 2. Pyrido[3,4-d]pyrimidin-4(3H)-one Derivatives., 59 (4): [PMID:26771203 ] [10.1021/acs.jmedchem.5b01538 ]