<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang Z</submitter><funding>NSFC</funding><pagination>17585-600</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6331867</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(9)</volume><pubmed_abstract>A novel series of benzenesulfonamide derivatives containing 4-aminobenzenesul-fonamide and α-amides branched valproic acid or 2,2-dimethylcyclopropanecarboxylic acid moieties were synthesized and screened for their anticonvulsant activities in mice maximal electroshock seizure (MES) and subcutaneous pentylenetetrazole (scPTZ) test. The activity experimental study showed that 2,2-dipropyl-N¹-(4-sulfamoylphenyl)malonamide (18b) had the lowest median effective dose (ED50) of 16.36 mg/kg in MES test, and 2,2-dimethyl-N-(4-sulfamoylphenyl)cyclopropane-1,1-dicarboxamide (12c) had the lowest ED50 of 22.50 mg/kg in scPTZ test, which resulted in the protective indexe (PI) of 24.8 and 20.4, respectively. These promising data suggest the new compounds have good potential as new class of anticonvulsan</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Synthesis and Pharmacological Evaluation of Novel Benzenesulfonamide Derivatives as Potential Anticonvulsant Agents.</pubmed_title><pmcid>PMC6331867</pmcid><funding_grant_id>81402882, 81273363, 81373254, 81301268</funding_grant_id><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Hu XM</pubmed_authors><pubmed_authors>Hong X</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Zhou X</pubmed_authors><pubmed_authors>Zeng XD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis and Pharmacological Evaluation of Novel Benzenesulfonamide Derivatives as Potential Anticonvulsant Agents.</name><description>A novel series of benzenesulfonamide derivatives containing 4-aminobenzenesul-fonamide and α-amides branched valproic acid or 2,2-dimethylcyclopropanecarboxylic acid moieties were synthesized and screened for their anticonvulsant activities in mice maximal electroshock seizure (MES) and subcutaneous pentylenetetrazole (scPTZ) test. The activity experimental study showed that 2,2-dipropyl-N¹-(4-sulfamoylphenyl)malonamide (18b) had the lowest median effective dose (ED50) of 16.36 mg/kg in MES test, and 2,2-dimethyl-N-(4-sulfamoylphenyl)cyclopropane-1,1-dicarboxamide (12c) had the lowest ED50 of 22.50 mg/kg in scPTZ test, which resulted in the protective indexe (PI) of 24.8 and 20.4, respectively. These promising data suggest the new compounds have good potential as new class of anticonvulsan</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Sep</publication><modification>2025-04-18T15:15:53.68Z</modification><creation>2019-03-26T22:39:27Z</creation></dates><accession>S-EPMC6331867</accession><cross_references><pubmed>26404228</pubmed><doi>10.3390/molecules200917585</doi></cross_references></HashMap>