European Journal of Medicinal Chemistry 2010-08-01

Synthesis and antileishmanial activity of piperoyl-amino acid conjugates.

Inder Pal Singh, Shreyans Kumar Jain, Amandeep Kaur, Sukhvinder Singh, Rajender Kumar, Prabha Garg, Shyam Sundar Sharma, Sunil Kumar Arora

Index: Eur. J. Med. Chem. 45 , 3439-3445, (2010)

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Abstract

Based on reported antileishmanial activity of naturally occurring alkaloid piperine and amino acid esters, their conjugates were synthesized by the hydrolysis of piperine to piperic acid followed by reaction with amino acid methyl esters. These conjugates were further converted to compounds with free carboxyl group and those with reduced double bonds. The synthesized compounds were evaluated for activity against promastigote and amastigote forms of L. donovani in vitro. All the compounds showed better activity than either piperine or the amino acid methyl esters. Piperoyl-valine methyl ester was the most active compound showing an IC50 of 0.075 mM against the amastigotes. Two active compounds were evaluated for in vivo activity in golden hamster model of leishmaniasis.

Related Compounds

  • H-Tyr-OMe
  • Piperine
  • Miltefosine

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