2,2-dichloro-N-(5-methyl-3-(3-(trifluoromethyl)phenyl)thiazol-2(3H)-ylidene)acetamide

ID: ALA2270028

Chembl Id: CHEMBL2270028

PubChem CID: 76312417

Max Phase: Preclinical

Molecular Formula: C13H9Cl2F3N2OS

Molecular Weight: 369.20

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1cn(-c2cccc(C(F)(F)F)c2)/c(=N/C(=O)C(Cl)Cl)s1

Standard InChI:  InChI=1S/C13H9Cl2F3N2OS/c1-7-6-20(12(22-7)19-11(21)10(14)15)9-4-2-3-8(5-9)13(16,17)18/h2-6,10H,1H3/b19-12-

Standard InChI Key:  ZBPNQZUMVHBPQA-UNOMPAQXSA-N

Associated Targets(non-human)

Ipomoea nil (52 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Abutilon theophrasti (831 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Echinochloa frumentacea (115 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: 369.20Molecular Weight (Monoisotopic): 367.9765AlogP: 4.10#Rotatable Bonds: 2
Polar Surface Area: 34.36Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.39CX LogD: 4.39
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.73Np Likeness Score: -1.73

References

1. Sanemitsu Y, Kawamura S, Satoh J, Katayama T, Hashimoto S.  (2006)  Synthesis and herbicidal activity of 2-acylimino-3-phenyl-1,3-thiazolines—A new family of bleaching herbicides—,  31  (3): [10.1584/jpestics.31.305]

Source