ID: ALA206241

Max Phase: Preclinical

Molecular Formula: C13H8Cl2F4N2

Molecular Weight: 339.12

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  FC1CCc2nn(-c3c(Cl)cc(C(F)(F)F)cc3Cl)cc21

Standard InChI:  InChI=1S/C13H8Cl2F4N2/c14-8-3-6(13(17,18)19)4-9(15)12(8)21-5-7-10(16)1-2-11(7)20-21/h3-5,10H,1-2H2

Standard InChI Key:  RPYIFLNKXOBNLG-UHFFFAOYSA-N

Associated Targets(non-human)

GABA receptor subunit 76 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

GABA-A receptor; anion channel 216 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Musca domestica 713 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ctenocephalides felis 292 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: 339.12Molecular Weight (Monoisotopic): 338.0001AlogP: 5.15#Rotatable Bonds: 1
Polar Surface Area: 17.82Molecular Species: NEUTRALHBA: 2HBD: 0
#RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 1.87CX LogP: 4.69CX LogD: 4.69
Aromatic Rings: 2Heavy Atoms: 21QED Weighted: 0.66Np Likeness Score: -1.06

References

1. Meegalla SK, Doller D, Liu R, Sha D, Lee Y, Soll RM, Wisnewski N, Silver GM, Dhanoa D..  (2006)  Synthesis and insecticidal activity of fluorinated 2-(2,6-dichloro-4-trifluoromethylphenyl)-2,4,5,6-tetrahydrocyclopentapyrazoles.,  16  (6): [PMID:16386419] [10.1016/j.bmcl.2005.12.012]

Source