(E)-N-((6-chloropyridin-3-yl)methyl)-N'-cyano-N-isopropylacetimidamide

ID: ALA2287447

Chembl Id: CHEMBL2287447

PubChem CID: 76327375

Max Phase: Preclinical

Molecular Formula: C12H15ClN4

Molecular Weight: 250.73

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  C/C(=N\C#N)N(Cc1ccc(Cl)nc1)C(C)C

Standard InChI:  InChI=1S/C12H15ClN4/c1-9(2)17(10(3)16-8-14)7-11-4-5-12(13)15-6-11/h4-6,9H,7H2,1-3H3/b16-10+

Standard InChI Key:  OBFKQWMXNMAWLZ-MHWRWJLKSA-N

Associated Targets(non-human)

Abdominal central nerve cord (25 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

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: 250.73Molecular Weight (Monoisotopic): 250.0985AlogP: 2.84#Rotatable Bonds: 3
Polar Surface Area: 52.28Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.64CX LogP: 1.89CX LogD: 1.89
Aromatic Rings: 1Heavy Atoms: 17QED Weighted: 0.36Np Likeness Score: -1.77

References

1. KIRIYAMA K, ITAZU Y, KAGABU S, NISHIMURA K.  (2003)  Insecticidal and Neuroblocking Activities of Acetamiprid and Related Compounds,  28  (1): [10.1584/jpestics.28.8]

Source