Microwave-assisted synthesis and anticonvulsant activity of 5,6-bisaryl-1,2,4-triazine-3-thiol derivatives
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A. Foroumadi | S. Emami | N. Naderi | H. Irannejad | Sakineh Dadashpour | Roja Qobadi Ghadikolaei | Tina Zafari | Ali Mazar-Atabaki
[1] O. Firuzi,et al. Design, synthesis and biological evaluation of novel anti-cytokine 1,2,4-triazine derivatives. , 2013, Bioorganic & medicinal chemistry.
[2] N. Naderi,et al. Modulation of Anticonvulsant Effects of Cannabinoid Compounds by GABA-A Receptor Agonist in Acute Pentylenetetrazole Model of Seizure in Rat , 2011, Neurochemical Research.
[3] Azim Dehghani Amirabad,et al. Inhibition of LPS-induced apoptosis in differentiated-PC12 cells by new triazine derivatives through NF-κB-mediated suppression of COX-2 , 2010, Neurochemistry International.
[4] D. Kaushik,et al. Design & synthesis of 2-(substituted aryloxy)-5-(substituted benzylidene)-3-phenyl-2,5-dihydro-1H-[1,2,4] triazin-6-one as potential anticonvulsant agents. , 2010, European journal of medicinal chemistry.
[5] Mohammad Sharifzadeh,et al. Synthesis and in vitro evaluation of novel 1,2,4-triazine derivatives as neuroprotective agents. , 2010, Bioorganic & medicinal chemistry.
[6] N. Siddiqui,et al. Triazole incorporated thiazoles as a new class of anticonvulsants: design, synthesis and in vivo screening. , 2010, European journal of medicinal chemistry.
[7] J. Sangshetti,et al. One pot synthesis and SAR of some novel 3-substituted 5,6-diphenyl-1,2,4-triazines as antifungal agents. , 2010, Bioorganic & medicinal chemistry letters.
[8] Christian Capello,et al. What is a green solvent? A comprehensive framework for the environmental assessment of solvents , 2007 .
[9] G. V. Suresh Kumar,et al. Synthesis and anticonvulsant activity of some potent 5,6-bis aryl 1,2,4-triazines , 2007, Journal of Zhejiang University SCIENCE B.
[10] C. J. Landmark. Targets for antiepileptic drugs in the synapse. , 2006, Medical science monitor : international medical journal of experimental and clinical research.
[11] C. Oliver Kappe,et al. The impact of microwave synthesis on drug discovery , 2006, Nature Reviews Drug Discovery.
[12] M. Heravi,et al. One‐Pot Synthesis of Some Nitrogen and Sulfur Heterocycles Using Thiosemicarbazide under Microwave Irradiation in a Solventless System. , 2006 .
[13] M. Heravi,et al. One-Pot Synthesis of Some Nitrogen and Sulfur Heterocycles Using Thiosemicarbazide Under Microwave Irradiation in a Solventless System , 2006 .
[14] W. Shipe,et al. Accelerating lead development by microwave-enhanced medicinal chemistry. , 2005, Drug discovery today. Technologies.
[15] H. Lankau,et al. Synthesis, anticonvulsant activity, and structure-activity relationships of sodium channel blocking 3-aminopyrroles. , 1998, Journal of medicinal chemistry.
[16] T. Bhalla,et al. Synthesis and pharmacological evaluation of 1,2,4-triazine and its congeners. , 1995, Bollettino chimico farmaceutico.
[17] W. Löscher,et al. The role of technical, biological and pharmacological factors in the laboratory evaluation of anticonvulsant drugs. IV. Protective indices , 1991, Epilepsy Research.
[18] W. Löscher,et al. The role of technical, biological and pharmacological factors in the laboratory evaluation of anticonvulsant drugs. III. Pentylenetetrazole seizure models , 1991, Epilepsy Research.
[19] I. Lalezari,et al. A ONE-STEP SYNTHESIS OF THE AS-TRIAZINE SYSTEM , 1970 .
[20] Woodbury La,et al. Design and use of a new electroshock seizure apparatus, and analysis of factors altering seizure threshold and pattern. , 1952 .
[21] L. Woodbury,et al. Stimulus parameters for electroshock seizures in rats. , 1952, The American journal of physiology.
[22] V. Davenport,et al. Design and use of a new electroshock seizure apparatus, and analysis of factors altering seizure threshold and pattern. , 1952, Archives internationales de pharmacodynamie et de therapie.