ID: ALA3228792

Max Phase: Preclinical

Molecular Formula: C14H19N3O

Molecular Weight: 245.33

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCc1ccc2ccc(=O)n(CCN(C)C)c2n1

Standard InChI:  InChI=1S/C14H19N3O/c1-4-12-7-5-11-6-8-13(18)17(14(11)15-12)10-9-16(2)3/h5-8H,4,9-10H2,1-3H3

Standard InChI Key:  FDYGQUIPVAUOKO-UHFFFAOYSA-N

Associated Targets(non-human)

Histamine H2 receptor 143 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Canis familiaris 36305 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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

Properties

Molecular Weight: 245.33Molecular Weight (Monoisotopic): 245.1528AlogP: 1.52#Rotatable Bonds: 4
Polar Surface Area: 38.13Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.07CX LogP: 1.69CX LogD: 0.93
Aromatic Rings: 2Heavy Atoms: 18QED Weighted: 0.82Np Likeness Score: -1.28

References

1. Bolhofer WA, Hoffman JM, Habecker CN, Pietruszkiewicz AM, Cragoe EJ, Torchiana ML..  (1979)  Inhibition of gastric acid secretion by 1,8-naphthyridin-2(1H)-ones.,  22  (3): [PMID:423213] [10.1021/jm00189a016]

Source