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5-(-4'-methylphenyl)-1,3-diphenylpyrazole ID: ALA3309267
Chembl Id: CHEMBL3309267
Cas Number: 16151-06-7
PubChem CID: 14532338
Max Phase: Preclinical
Molecular Formula: C22H18N2
Molecular Weight: 310.40
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: Cc1ccc(-c2cc(-c3ccccc3)nn2-c2ccccc2)cc1
Standard InChI: InChI=1S/C22H18N2/c1-17-12-14-19(15-13-17)22-16-21(18-8-4-2-5-9-18)23-24(22)20-10-6-3-7-11-20/h2-16H,1H3
Standard InChI Key: HBLZCAKQOWHDPU-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: 310.40Molecular Weight (Monoisotopic): 310.1470AlogP: 5.51#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: 1.56CX LogP: 6.17CX LogD: 6.17Aromatic Rings: 4Heavy Atoms: 24QED Weighted: 0.49Np Likeness Score: -1.24
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 ]