4-(trifluoromethyl)-N-(4-(trifluoromethyl)phenyl)benzamide

ID: ALA5288020

Chembl Id: CHEMBL5288020

Max Phase: Preclinical

Molecular Formula: C15H9F6NO

Molecular Weight: 333.23

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(Nc1ccc(C(F)(F)F)cc1)c1ccc(C(F)(F)F)cc1

Standard InChI:  InChI=1S/C15H9F6NO/c16-14(17,18)10-3-1-9(2-4-10)13(23)22-12-7-5-11(6-8-12)15(19,20)21/h1-8H,(H,22,23)

Standard InChI Key:  LFKUJYIIONKBSK-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5288020

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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: 333.23Molecular Weight (Monoisotopic): 333.0588AlogP: 4.98#Rotatable Bonds: 2
Polar Surface Area: 29.10Molecular Species: NEUTRALHBA: 1HBD: 1
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.82CX LogD: 4.82
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.77Np Likeness Score: -1.24

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