4-cyano-N-phenylbenzamide

ID: ALA5284299

Chembl Id: CHEMBL5284299

Max Phase: Preclinical

Molecular Formula: C14H10N2O

Molecular Weight: 222.25

Associated Items:

Names and Identifiers

Canonical SMILES:  N#Cc1ccc(C(=O)Nc2ccccc2)cc1

Standard InChI:  InChI=1S/C14H10N2O/c15-10-11-6-8-12(9-7-11)14(17)16-13-4-2-1-3-5-13/h1-9H,(H,16,17)

Standard InChI Key:  PMOXWVIRAXTQPK-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5284299

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Associated Targets(Human)

HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Schistosoma mansoni (6170 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: 222.25Molecular Weight (Monoisotopic): 222.0793AlogP: 2.81#Rotatable Bonds: 2
Polar Surface Area: 52.89Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 2.92CX LogD: 2.92
Aromatic Rings: 2Heavy Atoms: 17QED Weighted: 0.85Np Likeness Score: -1.76

References

1. Kanyanta M, Lengwe C, Mambwe D, Francisco KR, Liu LJ, Uli Sun Y, Amarasinghe DK, Caffrey CR, Mubanga Cheuka P..  (2023)  Activity of N-phenylbenzamide analogs against the neglected disease pathogen, Schistosoma mansoni.,  82  [PMID:36736493] [10.1016/j.bmcl.2023.129164]

Source