4-(1H-benzo[d]imidazol-2-yl)-6-methyl-2H-chromen-2-one

ID: ALA5282026

Chembl Id: CHEMBL5282026

Max Phase: Preclinical

Molecular Formula: C17H12N2O2

Molecular Weight: 276.30

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1ccc2oc(=O)cc(-c3nc4ccccc4[nH]3)c2c1

Standard InChI:  InChI=1S/C17H12N2O2/c1-10-6-7-15-11(8-10)12(9-16(20)21-15)17-18-13-4-2-3-5-14(13)19-17/h2-9H,1H3,(H,18,19)

Standard InChI Key:  LBTVJXDFHFMLIN-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5282026

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Associated Targets(non-human)

Bacillus flexus (54 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas (460 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 276.30Molecular Weight (Monoisotopic): 276.0899AlogP: 3.64#Rotatable Bonds: 1
Polar Surface Area: 58.89Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.45CX Basic pKa: 2.84CX LogP: 3.39CX LogD: 3.39
Aromatic Rings: 4Heavy Atoms: 21QED Weighted: 0.54Np Likeness Score: -0.66

References

1. Qin HL, Zhang ZW, Ravindar L, Rakesh KP..  (2020)  Antibacterial activities with the structure-activity relationship of coumarin derivatives.,  207  [PMID:32971428] [10.1016/j.ejmech.2020.112832]

Source