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1-Benzyl-4-(3-phenoxypropyl)-1H-[1,2,3]triazole ID: ALA2151778
Chembl Id: CHEMBL2151778
PubChem CID: 71451206
Max Phase: Preclinical
Molecular Formula: C18H19N3O
Molecular Weight: 293.37
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: c1ccc(Cn2cc(CCCOc3ccccc3)nn2)cc1
Standard InChI: InChI=1S/C18H19N3O/c1-3-8-16(9-4-1)14-21-15-17(19-20-21)10-7-13-22-18-11-5-2-6-12-18/h1-6,8-9,11-12,15H,7,10,13-14H2
Standard InChI Key: QEMIBFSROWXPLM-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: 293.37Molecular Weight (Monoisotopic): 293.1528AlogP: 3.34#Rotatable Bonds: 7Polar Surface Area: 39.94Molecular Species: NEUTRALHBA: 4HBD: ┄#RO5 Violations: ┄HBA (Lipinski): 4HBD (Lipinski): ┄#RO5 Violations (Lipinski): ┄CX Acidic pKa: ┄CX Basic pKa: 0.46CX LogP: 3.92CX LogD: 3.92Aromatic Rings: 3Heavy Atoms: 22QED Weighted: 0.63Np Likeness Score: -1.52
References 1. Rivara M, Patel MK, Amori L, Zuliani V.. (2012) Inhibition of NaV1.6 sodium channel currents by a novel series of 1,4-disubstituted-triazole derivatives obtained via copper-catalyzed click chemistry., 22 (20): [PMID:22981330 ] [10.1016/j.bmcl.2012.08.067 ]