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N-(4-(Aminomethyl)phenyl)-5-methyl-2-hydroxybenzamide Hydrochloride ID: ALA4864566
Chembl Id: CHEMBL4864566
PubChem CID: 164624518
Max Phase: Preclinical
Molecular Formula: C15H17ClN2O2
Molecular Weight: 256.31
Molecule Type: Unknown
Associated Items:
Names and Identifiers Canonical SMILES: Cc1ccc(O)c(C(=O)Nc2ccc(CN)cc2)c1.Cl
Standard InChI: InChI=1S/C15H16N2O2.ClH/c1-10-2-7-14(18)13(8-10)15(19)17-12-5-3-11(9-16)4-6-12;/h2-8,18H,9,16H2,1H3,(H,17,19);1H
Standard InChI Key: QIBVZVHDRKDFOB-UHFFFAOYSA-N
Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: UnknownTopical: 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: 256.31Molecular Weight (Monoisotopic): 256.1212AlogP: 2.41#Rotatable Bonds: 3Polar Surface Area: 75.35Molecular Species: BASEHBA: 3HBD: 3#RO5 Violations: ┄HBA (Lipinski): 4HBD (Lipinski): 4#RO5 Violations (Lipinski): ┄CX Acidic pKa: 8.24CX Basic pKa: 9.30CX LogP: 1.51CX LogD: 0.84Aromatic Rings: 2Heavy Atoms: 19QED Weighted: 0.79Np Likeness Score: -0.95
References 1. Aït Amiri S, Deboux C, Soualmia F, Chaaya N, Louet M, Duplus E, Betuing S, Nait Oumesmar B, Masurier N, El Amri C.. (2021) Identification of First-in-Class Inhibitors of Kallikrein-Related Peptidase 6 That Promote Oligodendrocyte Differentiation., 64 (9.0): [PMID:33949859 ] [10.1021/acs.jmedchem.0c02175 ]