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N-3-Pyridyl-N'-[1-{4-(4-methoxyphenyloxy)pyridin-2-yl}piperidin-4-yl]thiourea ID: ALA4561463
Chembl Id: CHEMBL4561463
PubChem CID: 149212651
Max Phase: Preclinical
Molecular Formula: C23H25N5O2S
Molecular Weight: 435.55
Molecule Type: Unknown
Associated Items:
Names and Identifiers Canonical SMILES: COc1ccc(Oc2ccnc(N3CCC(NC(=S)Nc4cccnc4)CC3)c2)cc1
Standard InChI: InChI=1S/C23H25N5O2S/c1-29-19-4-6-20(7-5-19)30-21-8-12-25-22(15-21)28-13-9-17(10-14-28)26-23(31)27-18-3-2-11-24-16-18/h2-8,11-12,15-17H,9-10,13-14H2,1H3,(H2,26,27,31)
Standard InChI Key: XGWOIVPUVQXYIG-UHFFFAOYSA-N
Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: UnknownTopical: 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: 435.55Molecular Weight (Monoisotopic): 435.1729AlogP: 4.23#Rotatable Bonds: 6Polar Surface Area: 71.54Molecular Species: NEUTRALHBA: 6HBD: 2#RO5 Violations: ┄HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): ┄CX Acidic pKa: 13.34CX Basic pKa: 7.24CX LogP: 3.41CX LogD: 3.19Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.56Np Likeness Score: -1.71
References 1. Ogasawara D, Ichu TA, Jing H, Hulce JJ, Reed A, Ulanovskaya OA, Cravatt BF.. (2019) Discovery and Optimization of Selective and in Vivo Active Inhibitors of the Lysophosphatidylserine Lipase α/β-Hydrolase Domain-Containing 12 (ABHD12)., 62 (3): [PMID:30720278 ] [10.1021/acs.jmedchem.8b01958 ]