| Weight | 289.182 g/mol |
|---|---|
| Formula | C7H16INOS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Acetylthiocholine iodide (1866-15-5)
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- Hydrolysis of an acetylthiocholine by pralidoxime iodide (2-PAM) (Toxicology Letters, 2006)
- Comparative studies of indophenyl acetate and iodide salts of acetylthiocholine and butyrylthiocholine as esterase substrates (Comparative and General Pharmacology, 1972)
- Determination of rat serum esterase activities by an HPLC method using S-acetylthiocholine iodide and p-nitrophenyl acetate. (Analytical Biochemistry, 2008)
- Critical Evaluation of Acetylthiocholine Iodide and Acetylthiocholine Chloride as Substrates for Amperometric Biosensors Based on Acetylcholinesterase (Sensors, 2013)
- The liberation of thiocholine from acetylthiocholine (ASCh) by pralidoxime iodide (2=PAM) and other oximes (obidoxime and diacetylmonoxime). (Toxicology Letters, 2006)
- Hydrolysis of acetylthiocholine iodide and reactivation of phoxim-inhibited acetylcholinesterase by pralidoxime chloride, obidoxime chloride and trimedoxime (Archives of Toxicology, 2007)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCC(=O)SCC[N+](C)(C)C.[I-]
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InChIKeyNTBLZMAMTZXLBP-UHFFFAOYSA-M
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