Synthesis and Anticonvulsant Activity of Substituted-1,3-diazaspiro[4.5]decan-4-ones

被引:23
作者
Aboul-Enein, Mohamed Nabil [1 ]
El-Azzouny, Aida Abdel Sattar [1 ]
Saleh, Ola Ahmed [1 ]
Amin, Kamilia Mahmoud [2 ]
Maklad, Yousreya Ali [3 ]
Hassan, Rasha Mohamed [1 ]
机构
[1] Natl Res Ctr, Pharmaceut & Med Chem Dept, Med Chem Grp, Pharmaceut & Drug Ind Res Div, Giza 12622, Egypt
[2] Cairo Univ, Dept Pharmaceut Chem, Fac Pharm, Cairo, Egypt
[3] Natl Res Ctr, Pharmaceut & Med Chem Dept, Pharmacol Grp, Pharmaceut & Drug Ind Res Div, Giza 12622, Egypt
关键词
Anticonvulsants; 1,3-Diazaspiro[4,5]decan-4-ones; Epilepsy; ANTIEPILEPTIC DRUGS; POTENTIAL ANTICONVULSANTS; DERIVATIVES; EPILEPSY; DESIGN; MECHANISMS; EFFICACY; MODEL;
D O I
10.1002/ardp.201500092
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of novel spiroimidazolidinone derivatives 6a-d and 8a-x were synthesized and biologically evaluated for their anticonvulsant activity in the maximal electroshock seizure (MES) assay and the subcutaneous pentylenetetrazole (scPTZ) screening test. Compound 8w was the most active derivative in the scPTZ screening test with an ED50 value by about 5- and 83.6-fold lower than those of phenobarbital and ethosuximide as reference drugs, respectively. Most of the tested compounds exhibited moderate to weak activity in the MES screen test, except for 8a which displayed 100% protection at 0.09mmol/kg. Moreover, all the test compounds did not show any minimal motor impairment in the neurotoxicity test.
引用
收藏
页码:575 / 588
页数:14
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