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

Alternative Forms

  1. Parent:

    ALA4561463

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Associated Targets(non-human)

Abhd12 Monoacylglycerol lipase ABHD12 (104 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 435.55Molecular Weight (Monoisotopic): 435.1729AlogP: 4.23#Rotatable Bonds: 6
Polar 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: 3.19
Aromatic 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]

Source