| Weight | 256.328 g/mol |
|---|---|
| Formula | C9H23NO3PS+ |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 8 |
Echothiophate (6736-03-4)
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- Role of Water in Aging of Human Butyrylcholinesterase Inhibited by Echothiophate: The Crystal Structure Suggests Two Alternative Mechanisms of Aging (Biochemistry, 2005)
- The Tonographic Effects of Echothiophate (Phospholine) Iodide*: Reversal by Pyridine-2-Aldoxime Methiodide (P2AM) (American Journal of Ophthalmology, 1959)
- Systemic Effects Produced by Echothiophate Iodide in Treatment of Glaucoma (Archives of Ophthalmology, 1963)
- Allergic Contact Dermatitis to Echothiophate Iodide and Phenylephrine (Archives of Ophthalmology, 1979)
- Echothiophate-induced structural alterations in the anterior chamber angle of the cynomolgus monkey. (Investigative Ophthalmology & Visual Science, 1979)
- Clonidine protection from soman and echothiophate toxicity in mice (Life Sciences, 1986)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOP(=O)(OCC)SCC[N+](C)(C)C
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- Pubchem - Echothiophate
- Wikipedia - echothiophate
Echothiophate (Phospholine) is an irreversible acetylcholinesterase inhibitor.
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