4-hydroxybenzimidazole-5-carboxylic acid, 4-phenoxyphenylamide

ID: ALA211246

Chembl Id: CHEMBL211246

PubChem CID: 11846850

Max Phase: Preclinical

Molecular Formula: C20H15N3O3

Molecular Weight: 345.36

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(Nc1ccc(Oc2ccccc2)cc1)c1ccc2[nH]cnc2c1O

Standard InChI:  InChI=1S/C20H15N3O3/c24-19-16(10-11-17-18(19)22-12-21-17)20(25)23-13-6-8-15(9-7-13)26-14-4-2-1-3-5-14/h1-12,24H,(H,21,22)(H,23,25)

Standard InChI Key:  JKRNBJZHIMUSKU-UHFFFAOYSA-N

Associated Targets(non-human)

Parastagonospora nodorum (325 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SdhC Mitochondrial complex II; succinate dehydrogenase (14 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

Calculated Properties

Molecular Weight: 345.36Molecular Weight (Monoisotopic): 345.1113AlogP: 4.31#Rotatable Bonds: 4
Polar Surface Area: 87.24Molecular Species: NEUTRALHBA: 4HBD: 3
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: 6.58CX Basic pKa: 4.15CX LogP: 3.55CX LogD: 2.53
Aromatic Rings: 4Heavy Atoms: 26QED Weighted: 0.51Np Likeness Score: -0.91

References

1. Bolgunas S, Clark DA, Hanna WS, Mauvais PA, Pember SO..  (2006)  Potent inhibitors of the Qi site of the mitochondrial respiration complex III.,  49  (15): [PMID:16854082] [10.1021/jm060408s]

Source