SBIR/STTR Research Award

NON-PEPTIDES INHIBITORS OF ANTHRAX LETHAL FACTOR

Award identifier a3ea49241e70574daf9af41e1860a37e793ef0e3dc05735184b3ba61922fda52Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$754,259

Program and phase

SBIR · Phase II

Award year

2002

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
CENGENT THERAPEUTICS, 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): Bacillus anthracis, the cause of Anthrax, poses a considerable danger because of its potential use in bioterrorism. Respiratory anthrax infections are almost invariably fatal despite antibiotic treatment. Existing vaccines provide no protection against certain strains of B. anthracis. A small drug-like molecule that could inhibit the action of lethal factor, the zinc metalloprotease responsible for the lethal effects of bacillus anthracis, could provide significant protection against anthrax. Using patented and proprietary protein structure-based methods, Structural Bioinformatics Inc. extracted 3D-pharmacophore information from the computationally modeled LF substrate MAPKK1 during Phase I. After synthesis based on this pharmacophore, seven compounds with 1C50 100-fold selectivity against LF versus human metalloenzymes. To this end, refined pharmacophores and docking models will be developed by applying SBl's technology to crystal structures data for LF and LF/inhibitor complexes. The long-term goal of this project is to develop a clinically useful small molecule that blocks the toxic effects of bacillus anthracis.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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