The following articles (labelled with PubMed ID or TBD) are for your review
| PMID | Data | Article Title | Organization |
|---|
| 25781377 |
10 |
Synthesis and bioactivity of฿-substituted fosmidomycin analogues targeting 1-deoxy-D-xylulose-5-phosphate reductoisomerase. |
Universiteit Gent |
| 25254502 |
27 |
Binding modes of reverse fosmidomycin analogs toward the antimalarial target IspC. |
Heinrich Heine Universit£T |
| 25210872 |
13 |
Development of inhibitors of the 2C-methyl-D-erythritol 4-phosphate (MEP) pathway enzymes as potential anti-infective agents. |
University of Groningen |
| 24360562 |
3 |
The effect of chain length and unsaturation on Mtb Dxr inhibition and antitubercular killing activity of FR900098 analogs. |
George Washington University |
| 24032981 |
25 |
IspC as target for antiinfective drug discovery: synthesis, enantiomeric separation, and structural biology of fosmidomycin thia isosters. |
Lehrstuhl FÜR Biochemie |
| 23819803 |
32 |
DXR inhibition by potent mono- and disubstituted fosmidomycin analogues. |
Uppsala University |
| 17491006 |
1 |
Structures of Mycobacterium tuberculosis 1-deoxy-D-xylulose-5-phosphate reductoisomerase provide new insights into catalysis. |
Uppsala University |
| 21824775 |
6 |
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 |
| 21561155 |
17 |
Inhibition of 1-deoxy-D-xylulose-5-phosphate reductoisomerase by lipophilic phosphonates: SAR, QSAR, and crystallographic studies. |
Baylor College of Medicine |
| 31382119 |
45 |
Novel reverse thia-analogs of fosmidomycin: Synthesis and antiplasmodial activity. |
Heinrich Heine University D£Sseldorf |
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