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Design, synthesis and evaluation of newer 5,6-dihydropyrimidine-2(1H)-thiones as GABA-AT inhibitors for anticonvulsant potential.

Abstract：

:Several new 5,6-dihydropyrimidine-2(1H)-thione derivatives have been prepared and investigated for their potencies for anticonvulsant activity against maximal electroshock (MES) and subcutaneous pentylenetetrazole (scPTZ) test in mice. The acute neurotoxicity was measured by rotarod test. Compounds 3c and 3l were found active in both of the animal models. Further, in vitro GABA-AT enzyme activity assay was carried out to investigate the possible mechanism of action through GABA-AT inhibition. The most potent compounds 3c and 3l showed inhibitory potency (IC50) of 18.42μM and 19.23μM, respectively. The molecular modeling was performed for all the synthesized compounds. The docking results were found in concordant with the observed animal studies.

journal_name

Bioorg Chem

journal_title

Bioorganic chemistry

authors

Sahu M,Siddiqui N,Iqbal R,Sharma V,Wakode S

doi

10.1016/j.bioorg.2017.07.017

subject

Has Abstract

pub_date

2017-10-01 00:00:00

pages

166-178

eissn

0045-2068

issn

1090-2120

pii

S0045-2068(17)30412-1

journal_volume

74

pub_type

杂志文章

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