Synthesis and antiepileptic activity of schiff’s bases of dialkylamino alkoxy isatin derivatives

4Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.
Get full text

Abstract

In the present work, some new 5-[2(3)-dialkylamino alkoxy] Indole 3-thiosemicarbazone 2-ones and 5-[2(3)-dialkylamino alkoxy] Indole 3-hydrazone 2-one were prepared from 5-hydroxy isatin. The structures of the products were characterized by IR, NMR, and MASS Spectral studies. All the compounds were examined for antiepileptic activity by maximal electroshock seizure (MES) and pentylenetetrazole (PTZ) induced convulsion method. These compounds were also evaluated for their neurotoxicity study by rotarod method. Some of these compounds showed good antiepileptic activity when compared with standard drug Phenytoin and all the compounds showed less neurotoxicity when compared with standard drug Diazepam.

Cite

CITATION STYLE

APA

Swathi, K., & Sarangapani, M. (2015). Synthesis and antiepileptic activity of schiff’s bases of dialkylamino alkoxy isatin derivatives. Advances in Experimental Medicine and Biology, 822, 119–128. https://doi.org/10.1007/978-3-319-08927-0_13

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free