1-benzyl-4-(phenoxymethyl)-1H-1,2,3-triazole

ID: ALA272339

Chembl Id: CHEMBL272339

PubChem CID: 715186

Max Phase: Preclinical

Molecular Formula: C16H15N3O

Molecular Weight: 265.32

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  c1ccc(Cn2cc(COc3ccccc3)nn2)cc1

Standard InChI:  InChI=1S/C16H15N3O/c1-3-7-14(8-4-1)11-19-12-15(17-18-19)13-20-16-9-5-2-6-10-16/h1-10,12H,11,13H2

Standard InChI Key:  YXUKSJXOHNRFMK-UHFFFAOYSA-N

Alternative Forms

Associated Targets(Human)

CYP19A1 Tclin Cytochrome P450 19A1 (6099 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Scn8a Sodium channel protein type VIII alpha subunit (53 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 265.32Molecular Weight (Monoisotopic): 265.1215AlogP: 2.91#Rotatable Bonds: 5
Polar Surface Area: 39.94Molecular Species: NEUTRALHBA: 4HBD:
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 3.39CX LogD: 3.39
Aromatic Rings: 3Heavy Atoms: 20QED Weighted: 0.71Np Likeness Score: -1.75

References

1. Aufort M, Herscovici J, Bouhours P, Moreau N, Girard C..  (2008)  Synthesis and antibiotic activity of a small molecules library of 1,2,3-triazole derivatives.,  18  (3): [PMID:18086525] [10.1016/j.bmcl.2007.11.111]
2. Doiron J, Soultan AH, Richard R, Touré MM, Picot N, Richard R, Cuperlović-Culf M, Robichaud GA, Touaibia M..  (2011)  Synthesis and structure-activity relationship of 1- and 2-substituted-1,2,3-triazole letrozole-based analogues as aromatase inhibitors.,  46  (9): [PMID:21703734] [10.1016/j.ejmech.2011.05.074]
3. 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]

Source