Armine
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| Names
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Preferred IUPAC name
Ethyl 4-nitrophenyl ethylphosphonate
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| Identifiers
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CAS Number
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3D model (JSmol)
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| ChemSpider
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| KEGG
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| MeSH
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Armin
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| UNII
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InChI
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
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SMILES
CCOP(=O)(CC)Oc1ccc(cc1)[N+](=O)[O-]
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| Properties
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Chemical formula
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C10H14NO5P
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| Molar mass
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259.198 g·mol−1
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references
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Armine is an irreversible acetylcholinesterase inhibitor.[1] It is the ethylphosphonate analog of paraoxon.
See also
- Paraoxon
- Ro 3-0419
- Ro 3-0422
References
- ↑ 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. PMID 5881660.
Acetylcholine metabolism and transport modulators |
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Enzyme (modulators) | | ChAT |
- Inhibitors: 1-(-Benzoylethyl)pyridinium
- 2-(α-Naphthoyl)ethyltrimethylammonium
- 3-Chloro-4-stillbazole
- 4-(1-Naphthylvinyl)pyridine
- Acetylseco hemicholinium-3
- Acryloylcholine
- AF64A
- B115
- BETA
- CM-54,903
- N,N-Dimethylaminoethylacrylate
- N,N-Dimethylaminoethylchloroacetate
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| AChE | |
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| BChE |
- Inhibitors: Affinine
- Affinisine
- Conodurine
- Cymserine
- Ladostigil
- Profenamine (ethopropazine)
- Rivastigmine
- Tacrine
- ZINC-12613047
- Many of the other AChE inhibitors listed above
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Transporter (modulators) | | CHT |
- Inhibitors: Hemicholinium-3 (hemicholine)
- Triethylcholine
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| VAChT | |
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Release (modulators) | | Inhibitors |
- SNAP-25 inactivators: Botulinum toxin (A, C, E)
- VAMP inactivators: Botulinum toxin (B, D, F, G)
- Others: [[Chemistry:BungaroBungarotoxins (Beta-Bungarotoxin|β-bungarotoxin]], γ-bungarotoxin)
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| Enhancers |
- LPHN agonists: α-Latrotoxin
- Others: Atracotoxins (e.g., robustoxin, versutoxin)
- Crotoxin
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See also: Receptor/signaling modulators • Muscarinic acetylcholine receptor modulators • Nicotinic acetylcholine receptor modulators |
 | Original source: https://en.wikipedia.org/wiki/Armine (chemical). Read more |