ID: ALA323189

Max Phase: Preclinical

Molecular Formula: C20H19N3O4S

Molecular Weight: 397.46

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(C[S+]([O-])c2ncccc2C(=O)Nc2ccncc2)c(OC)c1

Standard InChI:  InChI=1S/C20H19N3O4S/c1-26-16-6-5-14(18(12-16)27-2)13-28(25)20-17(4-3-9-22-20)19(24)23-15-7-10-21-11-8-15/h3-12H,13H2,1-2H3,(H,21,23,24)

Standard InChI Key:  PXKLONWVHOFNCZ-UHFFFAOYSA-N

Associated Targets(Human)

ATP4A Tclin Potassium-transporting ATPase (493 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATP4B Potassium-transporting ATPase (475 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: 397.46Molecular Weight (Monoisotopic): 397.1096AlogP: 3.05#Rotatable Bonds: 7
Polar Surface Area: 96.40Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.90CX Basic pKa: 5.61CX LogP: 1.52CX LogD: 1.51
Aromatic Rings: 3Heavy Atoms: 28QED Weighted: 0.62Np Likeness Score: -0.92

References

1. Terauchi H, Tanitame A, Tada K, Nakamura K, Seto Y, Nishikawa Y..  (1997)  Nicotinamide derivatives as a new class of gastric H+/K(+)-ATPase inhibitors. 1. Synthesis and structure-activity relationships of N-substituted 2-(benzhydryl- and benzylsulfinyl)nicotinamides.,  40  (3): [PMID:9022797] [10.1021/jm9605593]

Source