Полные агонисты 5-HT1A-рецепторов
Физиологическим полным агонистом 5-HT1A подтипа серотониновых рецепторов является серотонин (5-гидрокситриптамин, 5-HT).
Список полных агонистов
Примечания
- Winsauer P. J., Rodriguez F. H., Cha A. E., Moerschbaecher J. M. Full and partial 5-HT1A receptor agonists disrupt learning and performance in rats (англ.) // J. Pharmacol. Exp. Ther. : journal. — 1999. — January (vol. 288, no. 1). — P. 335—347. — PMID 9862788.
- Griebel G., Misslin R., Pawlowski M., Guardiola Lemaître B., Guillaumet G., Bizot-Espiard J. Anxiolytic-like effects of a selective 5-HT1A agonist, S20244, and its enantiomers in mice. (англ.) // Neuroreport. : journal. — 1992. — Vol. 3, no. 1. — P. 84—86. — doi:10.1097/00001756-199201000-00022. — PMID 1351756.
- Simon P., Guardiola B., Bizot-Espiard J., Schiavi P., Costentin J. 5-HT1A receptor agonists prevent in rats the yawning and penile erections induced by direct dopamine agonists. (англ.) // Psychopharmacology : journal. — Springer, 1992. — Vol. 108, no. 1—2. — P. 47—50. — doi:10.1007/BF02245284. — PMID 1357709.
- Astier B., Lambás Señas L., Soulière F., Schmitt P., Urbain N., Rentero N., Bert L., Denoroy L., Renaud B., Lesourd M., Muñoz C., Chouvet G. In vivo comparison of two 5-HT1A receptors agonists alnespirone (S-20499) and buspirone on locus coeruleus neuronal activity. (англ.) // Eur J Pharmacol. : journal. — 2003. — Vol. 459, no. 1. — P. 17—26. — doi:10.1016/S0014-2999(02)02814-5. — PMID 12505530.
- Bardin L., Tarayre J. P., Malfetes N., Koek W., Colpaert F. C. Profound, non-opioid analgesia produced by the high-efficacy 5-HT(1A) agonist F 13640 in the formalin model of tonic nociceptive pain (англ.) // Pharmacology : journal. — 2003. — April (vol. 67, no. 4). — P. 182—194. — doi:10.1159/000068404. — PMID 12595749.
- Bruins Slot L. A., Koek W., Tarayre J. P., Colpaert F. C. Tolerance and inverse tolerance to the hyperalgesic and analgesic actions, respectively, of the novel analgesic, F 13640 (англ.) // European Journal of Pharmacology : journal. — 2003. — April (vol. 466, no. 3). — P. 271—279. — doi:10.1016/S0014-2999(03)01566-8. — PMID 12694810.
- Bardin L., Assié M. B., Pélissou M., Royer-Urios I., Newman-Tancredi A., Ribet J. P., Sautel F., Koek W., Colpaert F. C. Dual, hyperalgesic, and analgesic effects of the high-efficacy 5-hydroxytryptamine 1A (5-HT1A) agonist F 13640 [(3-chloro-4-fluoro-phenyl)-[4-fluoro-4-{[(5-methyl-pyridin-2-ylmethyl)-amino]-methyl}piperidin-1-yl]methanone, fumaric acid salt]: relationship with 5-HT1A receptor occupancy and kinetic parameters (англ.) // The Journal of Pharmacology and Experimental Therapeutics : journal. — 2005. — March (vol. 312, no. 3). — P. 1034—1042. — doi:10.1124/jpet.104.077669. — PMID 15528450.
- Colpaert F. C., Deseure K., Stinus L., Adriaensen H. High-efficacy 5-hydroxytryptamine 1A receptor activation counteracts opioid hyperallodynia and affective conditioning (англ.) // The Journal of Pharmacology and Experimental Therapeutics : journal. — 2006. — February (vol. 316, no. 2). — P. 892—899. — doi:10.1124/jpet.105.095109. — PMID 16254131.
- Deseure K., Bréand S., Colpaert F. C. Curative-like analgesia in a neuropathic pain model: parametric analysis of the dose and the duration of treatment with a high-efficacy 5-HT(1A) receptor agonist (англ.) // European Journal of Pharmacology : journal. — 2007. — July (vol. 568, no. 1—3). — P. 134—141. — doi:10.1016/j.ejphar.2007.04.022. — PMID 17512927.
- Bernard Vacher, Bernard Bonnaud, Wouter Koek. Pyridin-2-yl-methylamine derivatives, method of preparing and application as medicine. US Patent 6020345, May 21, 1999.
- Koek W., Patoiseau J. F., Assié M. B., et al. F 11440, a potent, selective, high efficacy 5-HT1A receptor agonist with marked anxiolytic and antidepressant potential (англ.) // The Journal of Pharmacology and Experimental Therapeutics : journal. — 1998. — October (vol. 287, no. 1). — P. 266—283. — PMID 9765347.
- Prinssen E. P., Colpaert F. C., Koek W. 5-HT1A receptor activation and anti-cataleptic effects: high-efficacy agonists maximally inhibit haloperidol-induced catalepsy (англ.) // European Journal of Pharmacology : journal. — 2002. — October (vol. 453, no. 2—3). — P. 217—221. — doi:10.1016/S0014-2999(02)02430-5. — PMID 12398907.
- Maurel J. L., Autin J. M., Funes P., Newman-Tancredi A., Colpaert F., Vacher B. High-efficacy 5-HT1A agonists for antidepressant treatment: a renewed opportunity (англ.) // Journal of Medicinal Chemistry : journal. — 2007. — October (vol. 50, no. 20). — P. 5024—5033. — doi:10.1021/jm070714l. — PMID 17803293.
- Newman-Tancredi A., Martel J. C., Assié M. B., et al. Signal transduction and functional selectivity of F15599, a preferential post-synaptic 5-HT1A receptor agonist (англ.) // British Journal of Pharmacology : journal. — 2009. — January (vol. 156, no. 2). — P. 338—353. — doi:10.1111/j.1476-5381.2008.00001.x. — PMID 19154445.
- Haj-Dahmane S., Jolas T., Laporte A. M., et al. Interactions of lesopitron (E-4424) with central 5-HT1A receptors: in vitro and in vivo studies in the rat (англ.) // European Journal of Pharmacology : journal. — 1994. — April (vol. 255, no. 1—3). — P. 185—196. — doi:10.1016/0014-2999(94)90097-3. — PMID 8026543.
- Monte A. P., Marona-Lewicka D., Lewis M. M., Mailman R. B., Wainscott D. B., Nelson D. L., Nichols D. E. Substituted naphthofurans as hallucinogenic phenethylamine-ergoline hybrid molecules with unexpected muscarinic antagonist activity (англ.) // Journal of Medicinal Chemistry : journal. — 1998. — June (vol. 41, no. 12). — P. 2134—2145. — doi:10.1021/jm980076u. — PMID 9622555.
- Foreman M. M., Fuller R. W., Rasmussen K., Nelson D. L., Calligaro D. O., Zhang L., Barrett J. E., Booher R. N., Paget C. J., Flaugh M. E. Pharmacological characterization of LY293284: A 5-HT1A receptor agonist with high potency and selectivity (англ.) // The Journal of Pharmacology and Experimental Therapeutics : journal. — 1994. — September (vol. 270, no. 3). — P. 1270—1281. — PMID 7523657.
- Matsuda T., Yoshikawa T., Suzuki M., Asano S., Somboonthum P., Takuma K., Nakano Y., Morita T., Nakasu Y., Kim H. S. Novel benzodioxan derivative, 5-(3-[((2S)-1,4-benzodioxan-2- ylmethyl)aminopropoxy)-1,3-benzodioxole HCl (MKC-242), with a highly potent and selective agonist activity at rat central serotonin1A receptors.] (англ.) // Japanese journal of pharmacology. — 1995. — Vol. 69, no. 4. — P. 357—366. — PMID 8786639.
- De Vry J., Schohe-Loop R., Heine H. G., Greuel J. M., Mauler F., Schmidt B., Sommermeyer H., Glaser T. Characterization of the aminomethylchroman derivative BAY x 3702 as a highly potent 5-hydroxytryptamine1A receptor agonist. (англ.) // The Journal of pharmacology and experimental therapeutics. — 1998. — Vol. 284, no. 3. — P. 1082—1094. — PMID 9495870.
- Dong J., de Montigny C., Blier P. Full agonistic properties of BAY x 3702 on presynaptic and postsynaptic 5-HT1A receptors electrophysiological studies in the rat hippocampus and dorsal raphe. (англ.) // The Journal of pharmacology and experimental therapeutics. — 1998. — Vol. 286, no. 3. — P. 1239—1247. — PMID 9732384.
- Romero A. G., Leiby J. A., McCall R. B., Piercey M. F., Smith M. W., Han F. Novel 2-substituted tetrahydro-3H-benz[e]indolamines: highly potent and selective agonists acting at the 5-HT1A receptor as possible anxiolytics and antidepressants. (англ.) // J Med Chem. : journal. — 1993. — Vol. 36, no. 15. — P. 2066—2074. — doi:10.1021/jm00067a003. — PMID 8101876.
- McCall R. B., Romero A. G., Bienkowski M. J., Harris D. W., McGuire J. C., Piercey M. F., Shuck M. E., Smith M. W., Svensson K. A., Schreur P. J., et al. Characterization of U-92016A as a selective, orally active, high intrinsic activity 5-hydroxytryptamine1A agonist. (англ.) // J Pharmacol Exp Ther. : journal. — 1994. — Vol. 271, no. 2. — P. 875—883. — PMID 7965808.
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