ID: ALA2253193

Max Phase: Preclinical

Molecular Formula: C15H8BrCl3N4O

Molecular Weight: 446.52

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(Nc1cc(Cl)ccc1Cl)c1cc(Br)nn1-c1ncccc1Cl

Standard InChI:  InChI=1S/C15H8BrCl3N4O/c16-13-7-12(23(22-13)14-10(19)2-1-5-20-14)15(24)21-11-6-8(17)3-4-9(11)18/h1-7H,(H,21,24)

Standard InChI Key:  LGAZYIUDPGPGNJ-UHFFFAOYSA-N

Associated Targets(non-human)

Culex pipiens pallens 759 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mythimna separata 3306 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: 446.52Molecular Weight (Monoisotopic): 443.8947AlogP: 5.24#Rotatable Bonds: 3
Polar Surface Area: 59.81Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.44CX Basic pKa: CX LogP: 5.23CX LogD: 5.23
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.60Np Likeness Score: -1.98

References

1. Dong WL, Xu JY, Xiong LX, Li ZM..  (2012)  Synthesis, structure and insecticidal activities of some novel amides containing N-pyridylpyrazole moeities.,  17  (9): [PMID:22941222] [10.3390/molecules170910414]

Source