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Antimicrobial Agents and Chemotherapy, February 2006, p. 474-479, Vol. 50, No. 2
0066-4804/06/$08.00+0 doi:10.1128/AAC.50.2.474-479.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
MycoLogics, Inc, 12635 E. Montview Blvd., Suite 215, Aurora, Colorado 80010,1 Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado 805232
Received 22 August 2005/ Returned for modification 28 September 2005/ Accepted 1 November 2005
Leishmania major is an important trypanosomatid pathogen that causes leishmaniasis, which is a serious disease in much of the Old World. Current treatments include a small number of antimony compounds that, while somewhat effective, are limited by serious side effects. We have screened a small portion of a unique chemical library and have found at least three novel compounds that are effective against L. tarentolae and L. major in vitro and in a murine macrophage model of L. major infection. These compounds were effective in both assays at doses significantly lower than those of sodium stibogluconate (Pentostam) and represent possible candidates for drug development.
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