3-(chloacetyl)-5-(naphth-2-ylmethyl)benzamide

ID: ALA263112

Chembl Id: CHEMBL263112

PubChem CID: 44450519

Max Phase: Preclinical

Molecular Formula: C20H16ClNO2

Molecular Weight: 337.81

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  NC(=O)c1cc(Cc2ccc3ccccc3c2)cc(C(=O)CCl)c1

Standard InChI:  InChI=1S/C20H16ClNO2/c21-12-19(23)17-9-14(10-18(11-17)20(22)24)7-13-5-6-15-3-1-2-4-16(15)8-13/h1-6,8-11H,7,12H2,(H2,22,24)

Standard InChI Key:  PNZDQKADCPAIMA-UHFFFAOYSA-N

Alternative Forms

Associated Targets(Human)

HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

protease Human rhinovirus A protease (1343 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rhinovirus B14 (1052 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: 337.81Molecular Weight (Monoisotopic): 337.0870AlogP: 3.95#Rotatable Bonds: 5
Polar Surface Area: 60.16Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 13.95CX Basic pKa: CX LogP: 4.00CX LogD: 4.00
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.57Np Likeness Score: -0.44

References

1. Maugeri C, Alisi MA, Apicella C, Cellai L, Dragone P, Fioravanzo E, Florio S, Furlotti G, Mangano G, Ombrato R, Luisi R, Pompei R, Rincicotti V, Russo V, Vitiello M, Cazzolla N..  (2008)  New anti-viral drugs for the treatment of the common cold.,  16  (6): [PMID:18248816] [10.1016/j.bmc.2007.12.030]

Source