Some Scaffolds as Anti-leishmanial Agents: An Review

Author:

Mahender Thatikayala1,Pankaj Wadhwa1,Kumar Singh Pankaj2,Ankur Vaidya3,Kumar Sahu Sanjeev1

Affiliation:

1. School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, Punjab 144401, India

2. Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad 500037, India

3. Pharmacy College Saifai, Uttar Pradesh University of Medical Sciences, Saifai, Etawah (U.P.), India

Abstract

: Leishmaniasis is a parasitic infectious neglected tropical disease transmitted to humans by the parasites of Leishmania species. Mainly three types of leishmaniasis cases such as visceral (VL), cutaneous (CL) and mucocutaneous leishmaniasis are usually observed. In many western countries, almost 700,000 to 1million peoples are suffering from leishmaniasis and it is estimated that around 26000 to 65000 deaths occurs annually. For its treatment few drugs are available however none of them are ideal to treat leishmaniasis due to long treatment, discomfort mode of administration, risk of high level toxicity, high resistance against etc. Hence so many patients are unable to take complete treatment due to the high drug resistance. The present review will focus on antileishmanial activity of reported derivatives of betacarboline, chalcone, azole, quinoline, quinazoline, benzimidazole, benzadiazapine, thiaazoles, semicarbazone and hydontoin analogues. We believe that this present study will helpful to researcher to design new antileishmanial agents.

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery,Pharmacology,General Medicine

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