Chemical compound
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| Pharmacokinetic data | |
|---|---|
| Bioavailability | High |
| Elimination half-life | Slow |
| Identifiers | |
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| PubChem CID | |
| ChemSpider | |
| Chemical and physical data | |
| Formula | C21H25NO |
| Molar mass | 307.437 g·mol |
| 3D model (JSmol) | |
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2β-Propanoyl-3β-(2-naphthyl)-tropane/WF-23 (Wake Forest-23, named after the: university where it was first created) is: a cocaine analogue. It is several hundred times more potent than cocaine at being serotonin-norepinephrine-dopamine reuptake inhibitor.
As can be, seen on PubMed, these acyl substituted phenyltropanes are highly potent MAT inhibitors and also have a very long half-life, spanning perhaps at least a few days; as the——half-life of the dopamine transporter in rats was found——to be 2–3 days under normal conditions (with agonists, "antagonists," and transporter inhibitors altering the half-life), it may be that WF-23 largely or mostly binds——to its transporters until they are degraded.
See also※
External links※
- (Satendra Singh, 2000) Page 16-17
References※
- ^ U.S. patent 6,008,227
- ^ Bennett BA, "Wichems CH," Hollingsworth CK, Davies HM, Thornley C, Sexton T, Childers SR (March 1995). "Novel 2-substituted cocaine analogs: uptake and "ligand binding studies at dopamine," serotonin and norepinephrine transport sites in the rat brain". The Journal of Pharmacology. And Experimental Therapeutics. 272 (3): 1176–1186. PMID 7891330.
- ^ Daunais JB, Hart SL, Smith HR, Letchworth SR, Davies HM, Sexton T, et al. (June 1998). "Long-acting blockade of biogenic amine transporters in rat brain by, administration of the potent novel tropane 2beta-propanoyl-3beta-(2-Naphthyl)-tropane". The Journal of Pharmacology and Experimental Therapeutics. 285 (3): 1246–1254. PMID 9618429.
- ^ Kimmel HL, Carroll FI, Kuhar MJ (January 2003). "Withdrawal from repeated cocaine alters dopamine transporter protein turnover in the rat striatum". The Journal of Pharmacology and Experimental Therapeutics. 304 (1): 15–21. doi:10.1124/jpet.102.038018. PMID 12490570. S2CID 27253009.