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5-(-4'-chlorophenyl)-3-phenyl-2-pyrazoline ID: ALA3309799
Chembl Id: CHEMBL3309799
Cas Number: 89144-73-0
PubChem CID: 4738347
Max Phase: Preclinical
Molecular Formula: C15H13ClN2
Molecular Weight: 256.74
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: Clc1ccc(C2CC(c3ccccc3)=NN2)cc1
Standard InChI: InChI=1S/C15H13ClN2/c16-13-8-6-12(7-9-13)15-10-14(17-18-15)11-4-2-1-3-5-11/h1-9,15,18H,10H2
Standard InChI Key: RXULPLUJSOLALC-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: 256.74Molecular Weight (Monoisotopic): 256.0767AlogP: 3.78#Rotatable Bonds: 2Polar Surface Area: 24.39Molecular Species: NEUTRALHBA: 2HBD: 1#RO5 Violations: ┄HBA (Lipinski): 2HBD (Lipinski): 1#RO5 Violations (Lipinski): ┄CX Acidic pKa: ┄CX Basic pKa: 3.15CX LogP: 3.80CX LogD: 3.80Aromatic Rings: 2Heavy Atoms: 18QED Weighted: 0.87Np Likeness Score: -0.90
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 ]