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(E)-N-((6-chloropyridin-3-yl)methyl)-N'-cyano-N-methylisobutyrimidamide ID: ALA2287454
Chembl Id: CHEMBL2287454
PubChem CID: 76316469
Max Phase: Preclinical
Molecular Formula: C12H15ClN4
Molecular Weight: 250.73
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: CC(C)/C(=N\C#N)N(C)Cc1ccc(Cl)nc1
Standard InChI: InChI=1S/C12H15ClN4/c1-9(2)12(16-8-14)17(3)7-10-4-5-11(13)15-6-10/h4-6,9H,7H2,1-3H3/b16-12+
Standard InChI Key: YPDQKWNPGRNLNW-FOWTUZBSSA-N
Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 250.73Molecular Weight (Monoisotopic): 250.0985AlogP: 2.70#Rotatable Bonds: 3Polar Surface Area: 52.28Molecular Species: NEUTRALHBA: 3HBD: 0#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0CX Acidic pKa: CX Basic pKa: 4.16CX LogP: 2.36CX LogD: 2.36Aromatic Rings: 1Heavy Atoms: 17QED Weighted: 0.36Np Likeness Score: -1.57
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 ]