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4-methylchalconephenylhydrazone ID: ALA3309794
Chembl Id: CHEMBL3309794
PubChem CID: 118706106
Max Phase: Preclinical
Molecular Formula: C22H20N2
Molecular Weight: 312.42
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: Cc1ccc(/C=C/C(=N\Nc2ccccc2)c2ccccc2)cc1
Standard InChI: InChI=1S/C22H20N2/c1-18-12-14-19(15-13-18)16-17-22(20-8-4-2-5-9-20)24-23-21-10-6-3-7-11-21/h2-17,23H,1H3/b17-16+,24-22+
Standard InChI Key: VFQQXYGTIDGKAW-KOARNGDQSA-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: 312.42Molecular Weight (Monoisotopic): 312.1626AlogP: 5.52#Rotatable Bonds: 5Polar Surface Area: 24.39Molecular Species: NEUTRALHBA: 2HBD: 1#RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): 1#RO5 Violations (Lipinski): 1CX Acidic pKa: ┄CX Basic pKa: 5.68CX LogP: 6.52CX LogD: 6.51Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.49Np Likeness Score: -0.64
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 ]