Synthesis, anticonvulsant activity, and molecular modeling studies of novel 1-phenyl/1-(4-chlorophenyl)-2-(1H-triazol-1-yl)ethanol ester derivatives

被引:9
作者
Dogan, Inci Selin [1 ]
Ozdemir, Zeynep [2 ]
Sari, Suat [3 ]
Bozbey, Irem [2 ]
Karakurt, Arzu [2 ]
Sarac, Selma [3 ]
机构
[1] Karadeniz Tech Univ, Fac Pharm, Dept Pharmaceut Chem, TR-61080 Trabzon, Turkey
[2] Inonu Univ, Fac Pharm, Dept Pharmaceut Chem, TR-44280 Malatya, Turkey
[3] Hacettepe Univ, Fac Pharm, Dept Pharmaceut Chem, TR-06100 Ankara, Turkey
关键词
Anticonvulsant activity; (Arylalkyl)azoles; Ester; Molecular docking; Synthesis; Triazole; BENZODIAZEPINE-BINDING-SITE; AMINOBUTYRIC ACID(A) RECEPTORS; OXIME ETHER DERIVATIVES; GABA(A) RECEPTORS; ANTIMICROBIAL ACTIVITIES; DRUG DEVELOPMENT; STRUCTURAL REQUIREMENTS; BIOLOGICAL EVALUATION; ACCURATE DOCKING; ALPHA(1) SUBUNIT;
D O I
10.1007/s00044-018-2225-6
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of new ester derivatives were synthesized by the reaction of various acids with 1-phenyl/1-(4-chlorophenyl)-2-(1H-triazol-1-yl)ethanol and in vivo screened for their anticonvulsant activity. The title compounds were screened against MES and ScM seizure tests according to a modified version of the Epilepsy Therapy Screening Program (ETSP) protocol of the National Institutes of Health (NIH). Their neurotoxic effects were evaluated by the rotarod test. All the compounds showed protection against MES and/or ScM-induced seizures at 30 mg/kg without neurotoxicity. More compounds were found active in the ScM test and at lower dose than the MES test. Physicochemical and pharmacokinetic profiles of the compounds were predicted by QikProp. Using molecular docking approach we tried to get insights into their possible anticonvulsant mechanisms.
引用
收藏
页码:2171 / 2186
页数:16
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