ID: ALA432440

Max Phase: Preclinical

Molecular Formula: C21H21N3O5S

Molecular Weight: 427.48

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cc(OC)c(OC)cc1C[S+]([O-])c1ncccc1C(=O)Nc1ccncc1

Standard InChI:  InChI=1S/C21H21N3O5S/c1-27-17-12-19(29-3)18(28-2)11-14(17)13-30(26)21-16(5-4-8-23-21)20(25)24-15-6-9-22-10-7-15/h4-12H,13H2,1-3H3,(H,22,24,25)

Standard InChI Key:  QYPWHSRHSWAEJL-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: 427.48Molecular Weight (Monoisotopic): 427.1202AlogP: 3.06#Rotatable Bonds: 8
Polar Surface Area: 105.63Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.90CX Basic pKa: 5.61CX LogP: 1.36CX LogD: 1.36
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.55Np Likeness Score: -0.76

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