Fosmidomycin
File:Fosmidomycin.svg | |
Systematic (IUPAC) name | |
---|---|
3-[Formyl(hydroxy)amino]propoylphosphonic acid | |
Identifiers | |
CAS Number | 66508-53-0 |
ATC code | none |
PubChem | CID 572 |
DrugBank | EXPT01469 |
ChemSpider | 555 |
Chemical data | |
Formula | C4H10NO5P |
Molar mass | 183.100 g/mol[[Script error: No such module "String".]] |
Fosmidomycin is an antibiotic that specifically inhibits DXP reductoisomerase, a key enzyme in the non-mevalonate pathway. It is a structural analogue of 2-C-methyl-D-erythrose 4-phosphate. It inhibits the E. coli enzyme with a KI value of 38 nM (4), MTB at 80 nM, and the Francisella enzyme at 99 nM [1].
The discovery of the non-mevalonate pathway in malaria parasites has indicated the use of fosmidomycin and other such inhibitors as anti-malarial drugs.[2] Indeed, fosmidomycin has been tested in combination treatment with clindamycin for treatment of malaria with favorable results.[3][4][5] It has been shown that an increase in copy number of the target enzyme (DXP reductoisomerase) correlates with in vitro fosmidomycin resistance in the lethal malaria parasite, Plasmodium falciparum.[6]
See also
References
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- ↑ Jawaid, S., Seidle, H., Zhou W, Abdirahman, H., Abadeer, M, Hix, JH, van Hoek, ML and RD Couch. Kinetic Characterization and Phosphoregulation of the Francisella tularensis 1-Deoxy-D-Xylulose 5-Phosphoate Reductoisomerase (MEP Synthase), PLOS One, 4(12): e8288. doi:10.1371/journal.pone.0008288
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