SBIR/STTR Research Award

Mitotic Kinesins: Novel Targets for Malaria Chemotherapy

Award identifier 6321e82b1dffbfc76e188e967f2ed706494cd6e518a5d129ab3657e8495e3af0Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$100,000

Program and phase

SBIR · Phase I

Award year

2003

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
CYTOKINETICS, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Malaria is a serious threat to human health in many regions of the world, with an estimated 500 million cases occurring annually. Increased global drug resistance by malaria parasites has rendered traditional therapies ineffective. Continued efforts to develop a protective vaccine are not expected to bear fruit in near future. New pharmaceutical agents with novel mechanisms of action are urgently needed to control the spread of this disease. This proposal intends to address this need by identifying small molecule inhibitors targeted to malarial kinesin motor proteins for future development into novel antiparasitic pharmaceutical candidates. Cytokinetics is uniquely suited for this task, being the leading drug discovery company with extensive experience in cytoskeletal targets. The proposed project will focus on two Plasmodium falciparum kinesin motor proteins with sequence homology to essential mitotic kinesins from several other species. These targets have proven to be attractive in other therapeutic areas. Cytokinetics has developed high throughput screens that allow rapid and systematic identification of potent inhibitors of kinesin motor activity. The goal for Phase I of this proposal is to determine the feasibility of uncovering small molecule agents with inhibitory activity against recombinant malarial kinesins in our high throughput screens. The objectives of the proposed work under Phase II are 1) to evaluate active compounds from the primary biochemical screens for antiproliferative activity against cultured P. falciparum and lack of toxicity towards mammalian cells, and 2) to characterize new malarial kinesin genes to maintain a pipeline of candidate targets.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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