2-chloro-N-(1-(3-chlorophenyl)-2-methylprop-1-enyl)-N-(2-methoxyethyl)acetamide

ID: ALA2288051

Chembl Id: CHEMBL2288051

PubChem CID: 15137838

Max Phase: Preclinical

Molecular Formula: C15H19Cl2NO2

Molecular Weight: 316.23

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COCCN(C(=O)CCl)C(=C(C)C)c1cccc(Cl)c1

Standard InChI:  InChI=1S/C15H19Cl2NO2/c1-11(2)15(12-5-4-6-13(17)9-12)18(7-8-20-3)14(19)10-16/h4-6,9H,7-8,10H2,1-3H3

Standard InChI Key:  AINRIHHQZIZQCK-UHFFFAOYSA-N

Associated Targets(non-human)

Pontederia vaginalis (622 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Schoenoplectiella juncoides (1014 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cyperus difformis (556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Echinochloa oryzicola (1513 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

Calculated Properties

Molecular Weight: 316.23Molecular Weight (Monoisotopic): 315.0793AlogP: 3.80#Rotatable Bonds: 6
Polar Surface Area: 29.54Molecular Species: NEUTRALHBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.09CX LogD: 3.09
Aromatic Rings: 1Heavy Atoms: 20QED Weighted: 0.75Np Likeness Score: -0.90

References

1. OKAMOTO H, KATO S, KOBUTANI T, OGASAWARA M, KONNAI M, TAKEMATSU T.  (1991)  Herbicidally Active N-(1-Arylethenyl)-2-chloroacetamides Bearing an Alkyloxyalkyl Moiety.,  55  (11): [10.1271/bbb1961.55.2737]

Source