acetamiprid

Synonyms: "acetamiprid", "mospilan", "(E)-N-((6-Chloropyridin-3-yl)methyl)-N'-cyano-N-methylacetimidamide", "N-((6-Chloro-3-pyridinyl)methyl)-N'-cyano-N-methylethanimidamide", "N-[(6-chloropyridin-3-yl)methyl]-N'-cyano-N-methylethanimidamide", "(E)-N-(6-chloro-3-pyridyl)methyl-N'-cyano-N-methylacetamidine", "ethanimidamide, N-[(6-chloro-3-pyridinyl)"

Source: Acetamiprid is an insecticide.

Identifiers:

IUPAC Name: N-[(6-chloropyridin-3-yl)methyl]-N'-cyano-N-methylethanimidamide
CAS Number: 135410-20-7
PubChem ID: 213021
InChiKey: WCXDHFDTOYPNIE-UHFFFAOYSA-N
Canonical SMILES: CC(=NC#N)N(C)CC1=CN=C(C=C1)Cl

Structural Properties:

Molecular Formula: C₁₀H₁₁ClN₄
Molecular Weight: 222.676

Pharmacophore Features:

Number of bond donors: 0
Number of bond acceptors: 3
Number of atoms different from hydrogen: 15

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2D structure (.sdf)
3D structure (.sdf)
3D structure (.mol2)
3D structure (.pdb)
3D structure (.pdbqt)

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Evidence Supporting This Chemical as an Endocrine Disruptor
TEDX List of Potential Endocrine Disruptors

Kong, D., Zhang, J., Hou, X., Zhang, S., Tan, J., Chen, Y., Yang, W., Zeng, J., Han, Y., Liu, X. and Xu, D., 2016. Acetamiprid inhibits testosterone synthesis by affecting the mitochondrial function and cytoplasmic adenosine triphosphate production in rat Leydig cells. Biology of reproduction, 96(1), pp.254-265. DOI: https://doi.org/10.1095/biolreprod.116.139550. URL: https://academic.oup.com/biolreprod/article/96/1/254/2734427.