Nucleoside hydrolase Inhibitors from natural products for Leishmania

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$211,698.00
Award Year:
2010
Program:
SBIR
Phase:
Phase I
Contract:
1R43AI082796-01A1
Agency Tracking Number:
AI082796
Solicitation Year:
n/a
Solicitation Topic Code:
NIAID
Solicitation Number:
n/a
Small Business Information
LIFEPHARMS, INC.
143 Shaw Street, New London, CT, 06320
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
172904067
Principal Investigator:
ESTEBAN MENA
(860) 405-9219
LIFEPHARMS@AOL.COM
Business Contact:
WENDY LOGIN
() -
lifepharms@aol.com
Research Institution:
n/a
Abstract
DESCRIPTION (provided by applicant): Our goal is to identify novel drugs for the treatment and chemoprophylaxis of Leishmania by blocking nucleoside hydrolase (NH) activity of this parasite. Leishmaniasis is a zoonosis and affects 12 million people in 88 c ountries, of which 72 are considered developing countries. It is estimated that 350 million people are at risk to infection by the different species of Leishmania. The disease assumed importance in the United States as many Desert Storm veterans were expos ed to sand flies; approximately 700 confirmed cases of cutaneous leishmaniasis were reported in 2003-2004 in soldiers returning from Iraq and Kuwait. Leishmania/HIV co-infection is emerging as an extremely serious, new disease and it is increasing in frequ ency. The Leishmania nucleoside hydrolase is an excellent candidate as a target for safe and effective pan-Leishmania drugs. These include i) the absence of NH activity in mammals, ii)its intracellular location, iii) and its constitutive expression in prom astigotes (the infective form transmitted by phlebotomine sand flies. We combined LifePharms' novel natural product library consisting of 120,000 semipurified compounds from field collected basidiomycetes and ascomycetes with MycoLogics' yeast-based HTS f or Leishmania nucleoside hydrolase (NH) inhibitors. From the 15,000 samples already screened, we identified 4 compounds that inhibit NH and are Leishmanicidal active against L. major promastigotes in culture. Here we propose to i) determine if the isolated lead compounds are active against infected mouse and human macrophages in vitro, ii). Isolate additional amounts of lead compound and chemically identify the active compounds, iii) screen an additional 30,000 samples from LifePharms semipure compound libr ary for in vitro activity using a MycoLogics' proprietary strain of yeast that requires the activity of the Leishmania major nucleoside hydrolase for growth on uridine as the sole source of uracil and the in vitro models of leishmaniasis. PUBLIC HEA LTH RELEVANCE: Leishmaniasis is a major public health risk throughout much of the tropical and subtropical world. The disease has assumed importance in the United States for due to presence of the US military in the Gulf War and it current deployments to I raq and Afghanistan many soldiers are bitten by sand flies and develop classic leishmaniasis presentations. Also, there is a concern that leishmaniasis could become more widespread in the United States. Our goal is to identify compounds that can be develop ed for the effective treatment of Leishmaniasis.

* information listed above is at the time of submission.

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