Several 2-thioglycosides were prepared. Glycosylation of 2-thioxo-thieno[2,3-d]-pyrimidines 5a,b with 1-bromo-2,3,5-tri-O-acetyl-alpha-d-arabinofuranosyle 7, 2,3,4,6-tetra-O-acetyl-alpha-d-glucopyranosyl and galacto-pyranosyl bromide 8a,b gave the protected beta-d-nuclosides 10a,b and 13a-d in high yields, which were transformed to deacetylated derivatives 14a,b and 15a-d. The structures of the compounds were elucidated by spectral and elemental analysis. Anti-inflammatory and Analgesic activities screening of the new compounds (at a dose of 100 mg/kg body weight) utilizing in vivo acute carrageenan-induced paw oedema standard method exhibited that the deacetylated derivatives 14a,b and 15a-d possess highly promising activities.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejmech.2009.12.056DOI Listing

Publication Analysis

Top Keywords

anti-inflammatory analgesic
8
deacetylated derivatives
8
derivatives 14ab
8
14ab 15a-d
8
synthesis biological
4
biological medicinal
4
medicinal significance
4
significance s-glycosido-thieno[23-d]-pyrimidines
4
s-glycosido-thieno[23-d]-pyrimidines anti-inflammatory
4
analgesic agents
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!