ID: ALA1520624

Max Phase: Preclinical

Molecular Formula: C11H9ClN2O3

Molecular Weight: 252.66

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(O)CCc1nc(-c2ccc(Cl)cc2)no1

Standard InChI:  InChI=1S/C11H9ClN2O3/c12-8-3-1-7(2-4-8)11-13-9(17-14-11)5-6-10(15)16/h1-4H,5-6H2,(H,15,16)

Standard InChI Key:  PZAHEYNFUFWABS-UHFFFAOYSA-N

Associated Targets(Human)

Thyroid stimulating hormone receptor 29986 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Chromobox protein homolog 1 92434 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ataxin-2 54410 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

TAR DNA-binding protein 43 40113 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Nonstructural protein 1 33327 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

PvdQ 215 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium verticillioides 912 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium decemcellulare 2 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium solani 1274 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Aedes aegypti 630 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

Properties

Molecular Weight: 252.66Molecular Weight (Monoisotopic): 252.0302AlogP: 2.41#Rotatable Bonds: 4
Polar Surface Area: 76.22Molecular Species: ACIDHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.21CX Basic pKa: CX LogP: 2.72CX LogD: -0.33
Aromatic Rings: 2Heavy Atoms: 17QED Weighted: 0.90Np Likeness Score: -1.89

References

1. PubChem BioAssay data set, 
2. Neves Filho RA, da Silva CA, da Silva CS, Brustein VP, do Amaral Ferraz Navarro DM, dos Santos FA, Alves LC, dos Santos Cavalcanti MG, Srivastava RM, das Graças Carneiro-Da-Cunha M..  (2009)  Improved microwave-mediated synthesis of 3-(3-aryl-1,2,4-oxadiazol-5-yl)propionic acids and their larvicidal and fungal growth inhibitory properties.,  57  (8): [PMID:19652406] [10.1248/cpb.57.819]
3. Oliveira VS, Pimenteira C, da Silva-Alves DC, Leal LL, Neves-Filho RA, Navarro DM, Santos GK, Dutra KA, dos Anjos JV, Soares TA..  (2013)  The enzyme 3-hydroxykynurenine transaminase as potential target for 1,2,4-oxadiazoles with larvicide activity against the dengue vector Aedes aegypti.,  21  (22): [PMID:24095017] [10.1016/j.bmc.2013.09.020]