ID: ALA206412

Max Phase: Preclinical

Molecular Formula: C13H7Cl2F5N2

Molecular Weight: 357.11

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  FC(F)(F)c1cc(Cl)c(-n2cc3c(n2)C(F)(F)CC3)c(Cl)c1

Standard InChI:  InChI=1S/C13H7Cl2F5N2/c14-8-3-7(13(18,19)20)4-9(15)10(8)22-5-6-1-2-12(16,17)11(6)21-22/h3-5H,1-2H2

Standard InChI Key:  KLDKXKALYGGCPV-UHFFFAOYSA-N

Associated Targets(non-human)

GABA-A receptor; anion channel 216 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

GABA receptor subunit 76 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ctenocephalides felis 292 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Musca domestica 713 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: 357.11Molecular Weight (Monoisotopic): 355.9906AlogP: 5.24#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: 0.00CX LogP: 5.41CX LogD: 5.41
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.64Np Likeness Score: -0.76

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