2-(4-phenyl-1H-1,2,3-triazol-1-yl)naphthalene-1,4-dione

ID: ALA2022335

Chembl Id: CHEMBL2022335

PubChem CID: 66556483

Max Phase: Preclinical

Molecular Formula: C18H11N3O2

Molecular Weight: 301.31

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C1C=C(n2cc(-c3ccccc3)nn2)C(=O)c2ccccc21

Standard InChI:  InChI=1S/C18H11N3O2/c22-17-10-16(18(23)14-9-5-4-8-13(14)17)21-11-15(19-20-21)12-6-2-1-3-7-12/h1-11H

Standard InChI Key:  JEJKJYMUGNKXFB-UHFFFAOYSA-N

Alternative Forms

Associated Targets(Human)

K562 (73714 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PBMC (10003 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
K562-Lucena 1 (34 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Trypanosoma cruzi (99888 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Leishmania amazonensis (3813 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Leishmania infantum (5912 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: 301.31Molecular Weight (Monoisotopic): 301.0851AlogP: 2.87#Rotatable Bonds: 2
Polar Surface Area: 64.85Molecular Species: NEUTRALHBA: 5HBD:
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 3.02CX LogD: 3.02
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.73Np Likeness Score: -0.51

References

1. da Silva Júnior EN, de Melo IM, Diogo EB, Costa VA, de Souza Filho JD, Valença WO, Camara CA, de Oliveira RN, de Araujo AS, Emery FS, dos Santos MR, de Simone CA, Menna-Barreto RF, de Castro SL..  (2012)  On the search for potential anti-Trypanosoma cruzi drugs: synthesis and biological evaluation of 2-hydroxy-3-methylamino and 1,2,3-triazolic naphthoquinoidal compounds obtained by click chemistry reactions.,  52  [PMID:22483633] [10.1016/j.ejmech.2012.03.039]
2. Guimarães TT, Pinto Mdo C, Lanza JS, Melo MN, do Monte-Neto RL, de Melo IM, Diogo EB, Ferreira VF, Camara CA, Valença WO, de Oliveira RN, Frézard F, da Silva EN..  (2013)  Potent naphthoquinones against antimony-sensitive and -resistant Leishmania parasites: synthesis of novel α- and nor-α-lapachone-based 1,2,3-triazoles by copper-catalyzed azide-alkyne cycloaddition.,  63  [PMID:23535320] [10.1016/j.ejmech.2013.02.038]
3. Xu Z, Zhao SJ, Liu Y..  (2019)  1,2,3-Triazole-containing hybrids as potential anticancer agents: Current developments, action mechanisms and structure-activity relationships.,  183  [PMID:31546197] [10.1016/j.ejmech.2019.111700]

Source