Benzoic acid 4-(2,3-dichloro-benzoyl)-2-methyl-phenyl ester

ID: ALA187531

Chembl Id: CHEMBL187531

PubChem CID: 44396575

Max Phase: Preclinical

Molecular Formula: C21H14Cl2O3

Molecular Weight: 385.25

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1cc(C(=O)c2cccc(Cl)c2Cl)ccc1OC(=O)c1ccccc1

Standard InChI:  InChI=1S/C21H14Cl2O3/c1-13-12-15(20(24)16-8-5-9-17(22)19(16)23)10-11-18(13)26-21(25)14-6-3-2-4-7-14/h2-12H,1H3

Standard InChI Key:  UWSVSSGDNCREHW-UHFFFAOYSA-N

Associated Targets(non-human)

Phospholipase A2 isozyme DE-I (8 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Phospholipase A2 (8 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Phospholipase A2 isozyme PLA-A (8 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: 385.25Molecular Weight (Monoisotopic): 384.0320AlogP: 5.75#Rotatable Bonds: 4
Polar Surface Area: 43.37Molecular Species: HBA: 3HBD:
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): #RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 6.82CX LogD: 6.82
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.33Np Likeness Score: -0.84

References

1. Khanum SA, Murari SK, Vishwanth BS, Shashikanth S..  (2005)  Synthesis of benzoyl phenyl benzoates as effective inhibitors for phospholipase A2 and hyaluronidase enzymes.,  15  (18): [PMID:15993585] [10.1016/j.bmcl.2005.06.012]

Source