Template:Methadone at opioid receptors, monoamine transporters, and the NMDA receptor
Jump to navigation
Jump to search
Compound | Affinities (Ki) | Ratios | Ref | ||||||
---|---|---|---|---|---|---|---|---|---|
MOR | DOR | KOR | SERT | NET | NMDAR | MOR:DOR:KOR | SERT:NET | ||
Methadone | 1.7 nM | 435 nM | 405 nM | ND | ND | 2,500–8,300 nM | 1:256:238 | ND | [1][2] |
Dextromethadone | 19.7 nM | 960 nM | 1,370 nM | 992 nM | 12,700 nM | 2,600–7,400 nM | 1:49:70 | 1:13 | [1][2] |
Levomethadone | 0.945 nM | 371 nM | 1,860 nM | 14.1 nM | 702 nM | 2,800–3,400 nM | 1:393:1968 | 1:50 | [1][2] |
Sources: [1][2] |
Template documentation
References
- ↑ 1.0 1.1 1.2 1.3 Codd EE, Shank RP, Schupsky JJ, Raffa RB (1995). "Serotonin and norepinephrine uptake inhibiting activity of centrally acting analgesics: structural determinants and role in antinociception". J. Pharmacol. Exp. Ther. 274 (3): 1263–70. PMID 7562497.
- ↑ 2.0 2.1 2.2 2.3 Gorman AL, Elliott KJ, Inturrisi CE (February 1997). "The d- and l-isomers of methadone bind to the non-competitive site on the N-methyl-D-aspartate (NMDA) receptor in rat forebrain and spinal cord". Neurosci. Lett. 223 (1): 5–8. doi:10.1016/S0304-3940(97)13391-2. PMID 9058409.