Tazomeline
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| Clinical data | |
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| ATC code | None |
| Identifiers | |
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| CAS Number | 131987-54-7 |
| PubChem (CID) | 131460 |
| ChemSpider | 116193 |
| UNII | QDP6S14W5W  |
| ChEMBL | CHEMBL131819 |
| Chemical and physical data | |
| Formula | C14H23N3S2 |
| Molar mass | 297.48 g/mol |
| 3D model (Jmol) | Interactive image |
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Tazomeline (LY-287,041) is a drug which acts as a non-selective muscarinic acetylcholine receptor agonist.[1][2] It was in clinical trials for the treatment of cognitive dysfunction such as that seen in Alzheimer's disease and schizophrenia, but development was apparently scrapped for unknown reasons.[1][2][3]
See also[edit]
References[edit]
- ^ a b Langmead CJ, Watson J, Reavill C (February 2008). "Muscarinic acetylcholine receptors as CNS drug targets". Pharmacology & Therapeutics. 117 (2): 232–43. doi:10.1016/j.pharmthera.2007.09.009. PMID 18082893.
- ^ a b Amos D Korczyn (October 2000). "Muscarinic M1 Agonists in the Treatment of Alzheimer's Disease". Expert Opinion on Investigational Drugs. 9 (10): 2259–2267(9). doi:10.1517/13543784.9.10.2259.
- ^ Mashkovskii MD, Glushkov RG (April 2001). "Drugs for the Treatment of Alzheimer's Disease". Pharmaceutical Chemistry Journal. 35 (4): 179–182. doi:10.1023/A:1010474325601.
