6

Ushbu maqolada sintetik birikma1-(4 ́-metoksifenil)-6,7-dimetoksi-1,2,3,4-tetragidroizoxinolinkam zaharli sinfga mansub ekanligi, 0.1; 0.5; 1.0; 5.0 va 10.0 mg/kg dozalarda psixo farmakologik faolliklari va tutqanoqqa qarshi solishtirma preparatlar karbamazepin va konvuleksdan qolishmasligi eksperimental tajribalar asosida tasdiqlangan

  • O'qishlar soni 6
  • Nashr sanasi 01-02-2025
  • Asosiy tilO'zbek
  • Sahifalar285-293
Ўзбек

Ushbu maqolada sintetik birikma1-(4 ́-metoksifenil)-6,7-dimetoksi-1,2,3,4-tetragidroizoxinolinkam zaharli sinfga mansub ekanligi, 0.1; 0.5; 1.0; 5.0 va 10.0 mg/kg dozalarda psixo farmakologik faolliklari va tutqanoqqa qarshi solishtirma preparatlar karbamazepin va konvuleksdan qolishmasligi eksperimental tajribalar asosida tasdiqlangan

Muallifning F.I.Sh. Lavozimi Tashkilot nomi
1 Sanoyev Z.I. ! Toshkent davlat stomatologiya instituti
Havola nomi
1 1.R. S. Fisher, W. van Emde Boas, W. Blume, C. Elger, P. Genton, P. Lee and J. J. Engel, “Epileptic Seizures and Epilepsy: Definitions Proposed by the International League against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE),” Epilepsia, Vol. 46, No. 4, 2005, pp. 470-472. doi:10.1111/j.0013-9580.2005.66104.x2.C. Gerlach and J. L. Krajewski, “Antiepileptic Drug Discovery and Development: What Have We Learned and Where Are We Going?” Pharmaceuticals, Vol. 3, No. 9, 2010, pp. 2884-2899. doi:10.3390/ph30928843.Chimirri, G. De Sarro, A. De Sarro, R. Gitto, S. Grasso, S. Quartarone, M. Zappalà, P. Giusti, V. Libri, A. Constanti and A. G. Chapman, “1-Aryl-3,5-dihydro-4H-2,3-benzodiazepin-4-ones: Novel AMPA Receptor Antagonists,” Journal of Medicinal Chemistry, Vol. 40, No. 8, 1997, pp. 1258-1269. doi:10.1021/jm960506l4.Chimirri, G. De Sarro, A. De Sarro, R. Gitto, S. Quartarone, M. Zappalà, A. Constanti and V. Libri, “3,5-Dihydro-4H-2,3-benzodiazepine-4-thiones: A New Class of AMPA Receptor Antagonists,” Journal of Medicinal Chemistry, Vol. 41, No. 18, 1998, pp. 3409-3416. doi:10.1021/jm98003935.M. Zappalà, R. Gitto, F. Bevacqua, S. Quartarone, A. Chimirri, M. Rizzo, G. D. Sarro and A. D. Sarro, “Synthesisand Evaluation of Pharmacological and Pharmacokinetic Properties of 11H-[1,2,4]triazolo[4,5-c][2,3] benzodiazepin-3(2H)-ones,” Journal of Medicinal Chemistry, Vol. 43, No. 25, 2000, pp. 4834-4839. doi:10.1021/jm001012y6.M. Zappalà, G. Postorino, N. Micale,S. Caccamese, N. Parrinello, G. Grazioso, G. Roda, F. S. Menniti, G. D. Sarro and S. Grasso, “Synthesis, Chiral Resolution, and Enantiopharmacology of a Potent 2,3-benzodiazepine Derivative as Noncompetitive AMPA Receptor Antagonis,” Journal of Medicinal Chemistry, Vol. 49, No. 2, 2006, pp. 575-581. doi:10.1021/jm050552y7.Y. Wang, C. S. Konkoy, V. I. Ilyin, K. E. Vanover, R. B. Carter, E. Weber, J. F. Keana, R. M. Woodward and S. X. Cai, “Synthesis of 7,8-(Methylenedioxy)-1-phenyl-3,5-dihydro-4H-2,3-benzodiazepin-4-ones as Novel and Potent Noncompetitive AMPA Receptor Antagonists,” Journal of Medicinal Chemistry, Vol. 41, No. 14, 1998, pp. 2621-2625. doi:10.1021/jm980168j8.G. Abrahám, S. Sólyom, E. Csuzdi, P. Berzsenyi , I. Ling, I. Tarnawa, T. Hámori, I. Pallagi, K. Horváth, F. Andrási,9.G. Kapus, L. G. J. Hársing, I. Király, M. Patthy and G. Horváth, “New Noncompetitive AMPA Antagonists,” Bioorganic & Medicinal Chemistry, Vol. 8, No. 8, 2000, pp. 2127-2143 doi:10.1016/S0968-0896(00)00133-410.T. Hámore, S. Sólyom, P. Berzsenyi, F. Andrási and I. Tarnawa, “Structural Analogues of Some Highly Active Non-Competitive AMPA Antagonists,” Bioorganic & Medicinal Chemistry Letters, Vol. 10, No. 9, 2000, pp. 899-902. doi:10.1016/S0960-894X(00)00117-711.S. Grasso, G. De Sarro, A. De Sarro, N. Micale, M. Zappalà, G. Puia, M. Baraldi and C. D. Micheli, “Synthesis and Anticonvulsant Activity of Novel and Potent 2,3-benzodiazepine AMPA/Kainate Receptor Antagonists,” Journal of Medicinal Chemistry, Vol. 42, 1999, pp. 4414-4421.doi:10.1021/jm991086d12.J. J. Luszczki, “Third-Generation Antiepileptic Drugs: Mechanisms of Action, Pharmacokinetics and Interactions,” Pharmacological Reports, Vol. 61, No. 2, 2009, pp. 197-21613.M. L. Barreca, R. Gitto, S. Quartarone, D. L. Luca, G. D. Sarro and A. Chimirri, “Pharmacophore Modeling as an Efficient Tool in the Discovery of Novel Noncompetitive,” Journal of Chemical Information and Modeling, Vol. 43, No. 2, 2003, pp. 651-655. doi:10.1021/ci025625q14.J. F. Howes and C. Bell, “Talampanel,” Neurotherapeutics, Vol. 4, No. 1, 2007, pp. 126-129.doi:10.1016/j.nurt.2006.11.00115.R. Gitto, R. Caruso, V. Orlando, S. Quartarone, M. L. Barreca, G. Ferreri, E. Russo, G. D. Sarro and A. Chimirri, “Synthesis and Anticonvulsant Properties of Tetrahydroisoquinoline Derivative,” Farmaco, Vol. 59, No. 1, 2004, pp. 7-12. doi:10.1016/j.farmac.2003.10.00316.Magdalena Białońet al. 1MeTIQ and olanzapine, despite their neurochemical impact, did not ameliorate performance in fear conditioning and social interaction tests in an MK-801 rat model of schizophrenia. Pharmacol Rep. 2021 Jan 6.doi: 10.1007/s43440-020-00209-9.17.Agnieszka Wąsik, Irena Romańska, Agnieszka Zelek-Molik, Lucyna Antkiewicz-Michaluk. Multiple Administration of Endogenous Amines TIQ and 1MeTIQ Protects Against a 6-OHDA-Induced Essential Fall of Dopamine Release in the Rat Striatum: In Vivo Microdialysis Study. Neurotox Res. 2018 Apr;33(3):523-531.doi: 10.1007/s12640-017-9824-8.Epub 2017 Oct 26.18.Lucyna Antkiewicz-Michaluket al. The mechanism of 1,2,3,4-tetrahydroisoquinolines neuroprotection: the importance of free radicals scavenging properties andinhibition of glutamate-induced excitotoxicity. J Neurochem. doi: 10.1111/j.1471-4159.2006.03756.x.Epub 2006 Mar 3.19.E. Możdżeń et al. 1,2,3,4-Tetrahydroisoquinoline produces an antidepressant-like effect in the forced swim test and chronic mild stress model of depression in the rat: Neurochemical correlates/ European Journal of Pharmacology 729 (2014) 107–11520.E. Możdżeń et al. Antidepressant-like effect of 1,2,3,4-tetrahydroisoquinoline and its methyl derivative in animal models of depression. Pharmacological Reports. PubDate2017-02-08, DOI:10.1016/j.pharep.2017.01.03221.Jurakulov Sh.N., Vinogradova V.I., Levkovich M.G. /Sintez 1-ariltetragidro-izoxinolinovix alkaloidov i ix analogov. //Ximiya prirod. soedin., 2013, s. 62-66.22.Sanoev Z.I., Mirzaev Yu.R. Pharmacological Activity Of The Possessing New Atypical Neuroleptics 1-Phenyltetrahydroisoquinoline Structure. The American Journal of Medical Sciences and Pharmaceutical Research Published: 2020|Pages:18-26 https://doi.org/10.37547/TAJMSPR/Volume02Issue08-0323.Sanoev Z.I., Mirzaev Y.R. Research of a new atypical neuroleptic 1-(3,4,-methylenedioxyphenyl)-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline on the central nervous system. Annals of the Romanian Society for Cell Biology, 2021, 25 (2), 2363–236924.Мирзаев Ю. Р., Саноев З. И., Жўрақулов Ш. Н., & Виноградова В. И. (2015). Психофармакологические свойства производного тетрагидроизохинолина. Международный научный журнал “Unity of Science” Вена, Австрия, 170-174.25.Yakubova L.K. Sanoev Z.I., Mirzaev Yu.R. Comparative pharmacological properties of a derivative of tetrahydroisoquinoline and seduxen. New Dey in Medicine. 2 (30/2) 2020, p. 365-36826.European Convention for the Protection of Vertebrate Animals Used for Experimental and Other Scientific Purposes, ETS No123, Strasbourg (1986).27.Mironov A.N. Rukovodstvo po provedeniyu doklinicheskix issledovaniy lekarstvennix sredstv. Chast pervaya. –M.: Grifi K, 2012. -944 s.28.Li, M. Anticonvulsant activity of B2, an adenosine analog, on chemical convulsant-induced seizures / M.Li, R. Kang, J. Shi [et al.] // PLoS One. –2013. –T. 8. –No. 6. –S. e67060.29.Khatoon, H. Evaluation of anticonvulsant and neuroprotective effects of camel milk in strychnine-induced seizure model / H. Khatoon, R. Najam, T. Mirza [et al.] // Asian Pacific Journal of Tropical Disease. –2015. –T. 5. –No. 10. –S. 817-820.
Kutilmoqda