Synthesis, Neurotoxicity and Anticonvulsant Study of Some Benzothiazole Analogs

被引:0
作者
Sethi, Kalyan K. [1 ]
Verma, Saurabh M. [2 ]
Prasanthi, Naru [2 ]
Annapurna, Mathrusri M. [1 ]
机构
[1] GITAM Univ, GITAM Inst Pharm, Visakhapatnam 530045, Andhra Pradesh, India
[2] Birla Inst Technol, Dept Pharmaceut Sci, Mesra Ranchi 835215, India
关键词
Benzothiazole sulfonamides; Carbonic Anhydrase Inhibitors; Neurotoxicity; Anticonvulsant; CARBONIC-ANHYDRASE INHIBITORS; DERIVATIVES; TARGETS;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of benzothiazole sulfonamides, thiosemicarbazones and guanidine derivatives were synthesized by different pathways and tested for the neurotoxicity studies by the Rotarod method. The minimal motor impairment, the significant results were found with compounds (7) and (3). Some of these compounds also showed anticonvulsant activity by decreasing the duration of convulsions in albino mice. Compound (3), (7) and also compound (2) were found to be increased in the onset of convulsion and other test drugs showed moderate protection and animals were recovered in these groups.
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页码:774 / 777
页数:4
相关论文
共 28 条
[21]   Carbonic anhydrases as targets for medicinal chemistry [J].
Supuran, Claudiu T. ;
Scozzafava, Andrea .
BIOORGANIC & MEDICINAL CHEMISTRY, 2007, 15 (13) :4336-4350
[22]   Carbonic Anhydrases as drug targets - An overview [J].
Supuran, Claudiu T. .
CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2007, 7 (09) :825-833
[23]   Carbonic anhydrase inhibitors [J].
Supuran, CT ;
Scozzafava, A ;
Casini, A .
MEDICINAL RESEARCH REVIEWS, 2003, 23 (02) :146-189
[24]   Indanesulfonamides as carbonic anhydrase inhibitors and anticonvulsant agents: Structure-activity relationship and pharmacological evaluation [J].
Thiry, Anne ;
Rolin, Stephanie ;
Vullo, Daniela ;
Frankart, Aureie ;
Scozzafava, Andrea ;
Dogne, Jean-Michel ;
Wouters, Johan ;
Supuran, Claudiu T. ;
Masereel, Bernard .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2008, 43 (12) :2853-2860
[25]   Synthesis of some new 4-styryltetrazolo[1,5-a]quinoxaline and 1-substituted-4-styryl[1,2,4]triazolo[4,3-a]quinoxaline derivatives as potent anticonvulsants [J].
Wagle, Shivananda ;
Adhikari, Airody Vasudeva ;
Kumari, Nalilu Suchetha .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2009, 44 (03) :1135-1143
[26]  
WILLAMS DA, 2002, FOYES PRINCIPLES MED, P182
[27]  
Yogeeswari P., 2005, Farmaco (Lausanne), V60, P1, DOI 10.1016/j.farmac.2004.09.001
[28]  
YOGEESWARI P, 2005, SYNTHESIS-STUTTGART, V59, P51