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Synthesis and kinetic evaluation of phosphomimetic inhibitors targeting type B ribose-5-phosphate isomerase from Mycobacterium tuberculosis

Courtiol-Legourd, Stephanie (author)
Univ Paris Saclay, Inst Chim Mol & Mat Orsay, CNRS, F-91400 Orsay, France.
Mariano, Sandrine (author)
Univ Paris Saclay, Inst Chim Mol & Mat Orsay, CNRS, F-91400 Orsay, France.
Foret, Johanna (author)
Univ Paris Saclay, Inst Chim Mol & Mat Orsay, CNRS, F-91400 Orsay, France.
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Roos, Annette K. (author)
Uppsala universitet,Science for Life Laboratory, SciLifeLab,Strukturbiologi
Mowbray, Sherry L, 1954- (author)
Uppsala universitet,Institutionen för cell- och molekylärbiologi,Science for Life Laboratory, SciLifeLab
Salmon, Laurent (author)
Univ Paris Saclay, Inst Chim Mol & Mat Orsay, CNRS, F-91400 Orsay, France.
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Univ Paris Saclay, Inst Chim Mol & Mat Orsay, CNRS, F-91400 Orsay, France Science for Life Laboratory, SciLifeLab (creator_code:org_t)
Elsevier, 2024
2024
English.
In: Bioorganic & Medicinal Chemistry Letters. - : Elsevier. - 0960-894X .- 1464-3405. ; 102
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Because tuberculosis is still a major health threat worldwide, identification of new drug targets is urgently needed. In this study, we considered type B ribose -5 -phosphate isomerase from Mycobacterium tuberculosis as a potential target, and addressed known problems of previous inhibitors in terms of their sensitivity to hydrolysis catalyzed by phosphatase enzymes, which impaired their potential use as drugs. To this end, we synthesized six novel phosphomimetic compounds designed to be hydrolytically stable analogs of the substrate ribose 5 -phosphate and the best known inhibitor 5-phospho-D-ribonate. The phosphate function was replaced by phosphonomethyl, sulfate, sulfonomethyl, or malonate groups. Inhibition was evaluated on type A and type B ribose -5phosphate isomerases, and stability towards hydrolysis using alkaline phosphatase and veal serum was assessed. One of the phosphomimetic analogs, 5-deoxy-5-phosphonomethyl-D-ribonate, emerged as the first strong and specific inhibitor of the M. tuberculosis enzyme that is resistant to hydrolysis.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

Enzyme inhibitors
Phosphate
Monosaccharides
Ribose
Isomerase
Tuberculosis

Publication and Content Type

ref (subject category)
art (subject category)

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