9 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Synthesis and bioactivity of฿-substituted fosmidomycin analogues targeting 1-deoxy-D-xylulose-5-phosphate reductoisomerase.
Universiteit Gent
Binding modes of reverse fosmidomycin analogs toward the antimalarial target IspC.
Heinrich Heine Universit£T
Development of inhibitors of the 2C-methyl-D-erythritol 4-phosphate (MEP) pathway enzymes as potential anti-infective agents.
University of Groningen
The effect of chain length and unsaturation on Mtb Dxr inhibition and antitubercular killing activity of FR900098 analogs.
George Washington University
IspC as target for antiinfective drug discovery: synthesis, enantiomeric separation, and structural biology of fosmidomycin thia isosters.
Lehrstuhl FÜR Biochemie
DXR inhibition by potent mono- and disubstituted fosmidomycin analogues.
Uppsala University
Structures of Mycobacterium tuberculosis 1-deoxy-D-xylulose-5-phosphate reductoisomerase provide new insights into catalysis.
Uppsala University
Substitution of the phosphonic acid and hydroxamic acid functionalities of the DXR inhibitor FR900098: an attempt to improve the activity against Mycobacterium tuberculosis.
Uppsala University