Armine (chemical)

In this article, we will explore the fascinating world of Armine (chemical) and its impact on society. Since time immemorial, Armine (chemical) has been the object of study, debate and reflection, capturing the attention of people of all ages, cultures and contexts. Throughout history, Armine (chemical) has played a fundamental role in the evolution of humanity, influencing key aspects of our daily lives. Through deep and insightful analysis, we will unravel the mysteries and complexities surrounding Armine (chemical), offering a broad and enriching vision that will allow us to better understand its meaning and relevance in the modern world. Immerse yourself in this exciting journey of discovery and broaden your horizons about Armine (chemical).

Armine
Names
Preferred IUPAC name
Ethyl 4-nitrophenyl ethylphosphonate
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
KEGG
MeSH Armin
UNII
  • InChI=1S/C10H14NO5P/c1-3-15-17(14,4-2)16-10-7-5-9(6-8-10)11(12)13/h5-8H,3-4H2,1-2H3
    Key: XXUJMEYKYHETBZ-UHFFFAOYSA-N
  • CCOP(=O)(CC)Oc1ccc(cc1)(=O)
Properties
C10H14NO5P
Molar mass 259.198 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).

Armine is an irreversible acetylcholinesterase inhibitor.[1] It is the ethylphosphonate analog of paraoxon.

See also

References

  1. ^ Reiner, E (December 1965). "Oxime reactivation of erythrocyte cholinesterase inhibited by ethyl p-nitrophenyl ethylphosphonate". The Biochemical Journal. 97 (3): 710–4. doi:10.1042/bj0970710. PMC 1264750. PMID 5881660.