Evaluation of analgesic, antipyretic, hypoglycemic and CNS depressant activity of 2-bromopopylamine hydrobromide, 3-bromopopyl ammonium bromide, ortho-amino aniline and benzimidazole-2-thiol in animal model

Synthetic compounds are encompassing the major ther apeutic classes of drugs which resemblance to the n atural or existing therapeutically active compounds. Herewith four synthetic compounds i.e. 2-bromopropylamine hydrobromide, 3-bromopropyl ammonium bromide, ortho -a...

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Detalhes bibliográficos
Principais autores: Md. Hamiduzzaman, Dey, Avijit, Mannan, Sultana Juhara, Rahman, S. M. Abdur
Outros Autores: Department of Pharmacy, BRAC University
Formato: Atigo
Publicado em: © 2014 Der Pharmacia Lettre 2016
Assuntos:
Acesso em linha:http://hdl.handle.net/10361/6821
Descrição
Resumo:Synthetic compounds are encompassing the major ther apeutic classes of drugs which resemblance to the n atural or existing therapeutically active compounds. Herewith four synthetic compounds i.e. 2-bromopropylamine hydrobromide, 3-bromopropyl ammonium bromide, ortho -amino aniline and benzimidazole-2-thiol were subje cted for analgesic, antipyretic, hypoglycemic and CNS de pressant activity in mice and rat model following s tandard protocol. Among the four supplied synthetic compoun ds, benzimidazole-2-thiol and 3-bromopropyl ammoniu m bromide at a dose of 50 mg/kg body wt revealed sign ificant analgesic activity with 37.85% and 42.85% i nhibition of writhing (P value < 0.001 in both cases). None of t he test samples showed antipyretic activity in rat model at a dose of 50 mg/kg body wt in comparable with standard ant ipyretic drug Paracetamol. On the other hand benzim idazole- 2-thiol reduced blood glucose level with respect to standard drug Glibenclamide having P value 0.00082 and 3- bromopropyl ammonium bromide lengthened the Na-phen obarbitone induced sleeping time having the P value 0.0009 which was statistically significant.