ID: ALA2289746

Max Phase: Preclinical

Molecular Formula: C15H17BrO2

Molecular Weight: 309.20

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COC(=O)[C@H]1[C@H](/C=C\c2ccc(Br)cc2)C1(C)C

Standard InChI:  InChI=1S/C15H17BrO2/c1-15(2)12(13(15)14(17)18-3)9-6-10-4-7-11(16)8-5-10/h4-9,12-13H,1-3H3/b9-6-/t12-,13+/m0/s1

Standard InChI Key:  OOJAYXQBLAOHBM-QDIXBRCLSA-N

Associated Targets(non-human)

Sitophilus zeamais 188 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Musca domestica 713 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Periplaneta americana 513 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Tuta absoluta 57 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ascia monuste 100 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: 309.20Molecular Weight (Monoisotopic): 308.0412AlogP: 3.91#Rotatable Bonds: 3
Polar Surface Area: 26.30Molecular Species: HBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.09CX LogD: 4.09
Aromatic Rings: 1Heavy Atoms: 18QED Weighted: 0.79Np Likeness Score: 0.79

References

1. Silvério FO, de Alvarenga ES, Moreno SC, Picanço MC..  (2009)  Synthesis and insecticidal activity of new pyrethroids.,  65  (8): [PMID:19418526] [10.1002/ps.1771]

Source