Drug Res (Stuttg) 2014; 64(02): 66-72
DOI: 10.1055/s-0033-1353184
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Synthesis and Anti-inflammatory Activities of Novel 5-(3,4-dichlorophenyl)-3-[(4-substitutedpiperazin-1-yl)methyl]-1,3,4-oxadiaxole-2(3H)-thiones

M. Koksal
1   Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Yeditepe University, Istanbul, Turkey
,
M. Yarim
1   Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Yeditepe University, Istanbul, Turkey
,
A. Erdal
2   Department of Pharmacology, Faculty of Medicine, Ondokuz Mayis University Samsun, Turkey
,
A. Bozkurt
2   Department of Physiology, Faculty of Medicine, Ondokuz Mayis University, Samsun, Turkey
› Author Affiliations
Further Information

Publication History

received 25 January 2013

accepted 12 July 2013

Publication Date:
28 August 2013 (online)

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Abstract

Purpose:

To synthesize a new series of 5-(3,4-dichlorophenyl)-3-[(4-substitutedpiperazin-1-yl)methyl]-1,3,4-oxadiaxole-2-thiones for their anti-inflammatory activity.

Methods:

The title compounds synthesized by Mannich reaction of prepared 5-(3,4-dichloro­phenyl)-1,3,4-oxadiazole-2-thione and appropriate substituted piperazine derivatives. The structures of the compounds were confirmed by IR, NMR and elemental analyses. The newly synthesized compounds were evaluated for their anti-inflammatory and ulcerogenic activities.

Results:

Most of the compounds were found to have significant anti-inflammatory profile in carrageenan footpad edema test. The compounds showed anti-inflammatory activity ranging from 30.6% to 57.8% inhibition.

Conclusion:

The compounds 5b, 5f, 5i, 5p and 5r showed most prominent anti-inflammatory activity with low gastric ulceration incidence than the reference drug indomethacine. These compounds could serve as lead molecules for further modifications.