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5-(-4'-chlorophenyl)-1,3-diphenylpyrazole ID: ALA3309804
Chembl Id: CHEMBL3309804
Cas Number: 27293-94-3
PubChem CID: 280869
Max Phase: Preclinical
Molecular Formula: C21H15ClN2
Molecular Weight: 330.82
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: Clc1ccc(-c2cc(-c3ccccc3)nn2-c2ccccc2)cc1
Standard InChI: InChI=1S/C21H15ClN2/c22-18-13-11-17(12-14-18)21-15-20(16-7-3-1-4-8-16)23-24(21)19-9-5-2-6-10-19/h1-15H
Standard InChI Key: JLUOYYKTIZVFDY-UHFFFAOYSA-N
Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 330.82Molecular Weight (Monoisotopic): 330.0924AlogP: 5.86#Rotatable Bonds: 3Polar Surface Area: 17.82Molecular Species: NEUTRALHBA: 2HBD: ┄#RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): ┄#RO5 Violations (Lipinski): 1CX Acidic pKa: ┄CX Basic pKa: 1.54CX LogP: 6.26CX LogD: 6.26Aromatic Rings: 4Heavy Atoms: 24QED Weighted: 0.46Np Likeness Score: -1.35
References 1. Raghav N, Singh M.. (2014) SAR studies of differently functionalized chalcones based hydrazones and their cyclized derivatives as inhibitors of mammalian cathepsin B and cathepsin H., 22 (15): [PMID:24913985 ] [10.1016/j.bmc.2014.05.037 ]