Abstract
Synthesis and Analgesic activity studies of Simple new Aspirin Enkephalin analogues
Hygeia.JD.Med.Vol.3(2),Oct.2011-March 2012.1-15.
Article Title: Synthesis andAnalgesic activity studies of Simple new Aspirin Enkephalin analogues
Authors: Balamani1* & M. Sekar2
1. Post Graduate and ResearchDepartment of Chemistry, Kongunadu Arts and Sciences College,Coimbatore-641 029, India.
2. Post Graduate and Research Department of Chemistry, SriRamakrishna Mission, Vidyalaya College of Arts and
Science, Coimbatore-641 020 India.
Article history: Received: 02October, 2010,
Revised: 27 November, 2010,
Accepted: 23 July, 2011,
Available online: 01 October2011
Abstract
Aspirinamino acid amides 1(a-f), Aspirin dipeptide amides 2(a-f). tri peptide amides 3(a-f) and tetra peptide amides 4a and 4c were Synthesized. The synthesis ofdipeptide amides were carried out in solution by stepwise elongation of thepeptide chain from the C-terminal amino acid by coupling one amino acid at atime using DCC/HOBt method. The analgesic activity was studied by acetic acidinduced writhing test. From the mean writhing values, it is evident that theentire sequence of the tetrapeptideamide namely, Gly-Gly-Phe-Met-NH2 isessential for the observed analgesic activity of compound A. And, the entiresequence of the tetra peptide amide namely, Gly-Gly-Phe-Leu-NH2 isessential for the observed analgesic activity of compound C. The decrease inanalgesic activity of these compounds is in the order, aspirin tripepitideamides > aspirin dipeptide amides > aspirin amino acid amides.
Keywords: Aspirin,analgesic activity, amino acid amide, di, tri, and tetra peptides
Article out line
1.Introduction
2.Scheme of synthesis
3.Analgesic activity(Acetic acid induced writhing test )
4.Results and discussion
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For correspondence
balamani_gokul@yahoo.co.in ,
Contact: +91 9942510532, Coimbatore, Tamilnadu, India 641029.
J. Balamani &M.Sekar, H.J.D.Med. Vol. 3 (2), 2011, pp.1-15.
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