The following articles (labelled with PubMed ID or TBD) are for your review
| PMID | Data | Article Title | Organization |
|---|
| 458818 |
26 |
Design of species- or isozyme-specific enzyme inhibitors. 1. Effect of thymidine substituents on affinity for the thymidine site of hamster cytoplasmic thymidine kinase. |
TBA |
| 17324575 |
133 |
Novel selective human mitochondrial kinase inhibitors: design, synthesis and enzymatic activity. |
University of Ferrara |
| 14584954 |
9 |
Synthesis and biological evaluation of 5-substituted derivatives of the potent antiherpes agent (north)-methanocarbathymine. |
National Cancer Institute-Frederick |
| 12930144 |
28 |
3'-C-branched-chain-substituted nucleosides and nucleotides as potent inhibitors of Mycobacterium tuberculosis thymidine monophosphate kinase. |
Ghent University |
| 12213066 |
41 |
Acyclic nucleoside analogues as novel inhibitors of human mitochondrial thymidine kinase. |
Instituto De Qu£Mica M£Dica (Csic) |
| 1331461 |
1 |
L-thymidine is phosphorylated by herpes simplex virus type 1 thymidine kinase and inhibits viral growth. |
Istituto Di Genetica Biochimica Ed Evoluzionistica |
| 2153206 |
19 |
Synthesis and in vitro evaluation of some modified 4-thiopyrimidine nucleosides for prevention or reversal of AIDS-associated neurological disorders. |
Michigan Cancer Foundation |
| 3033244 |
8 |
1-(2-Deoxy-2-fluoro-beta-D-arabinofuranosyl)-5-ethyluracil. A highly selective antiherpes simplex agent. |
TBA |
| 2989522 |
4 |
Synthesis and biological activities of 2-pyrimidinone nucleosides. 2. 5-Halo-2-pyrimidinone 2'-deoxyribonucleosides. |
TBA |
| 11392548 |
59 |
Design, synthesis and enzymatic activity of highly selective human mitochondrial thymidine kinase inhibitors. |
Universit£ |
| 20378362 |
20 |
3'-(1,2,3-Triazol-1-yl)-3'-deoxythymidine analogs as substrates for human and Ureaplasma parvum thymidine kinase for structure-activity investigations. |
Swedish University Agricultural Sciences |
| 20218622 |
59 |
3'-[4-Aryl-(1,2,3-triazol-1-yl)]-3'-deoxythymidine analogues as potent and selective inhibitors of human mitochondrial thymidine kinase. |
Ghent University |
| | 19 |
(2R, 4S, 5S)-1-(tetrahydro-4-hydroxy-5-methoxy-2-furanyl)thymine: a potent selective inhibitor of herpes simplex thymidine kinase |
TBA |
| 18556209 |
8 |
Anti-retroviral and cytostatic activity of 2',3'-dideoxyribonucleoside 3'-disulfides. |
Université |
| 18047266 |
5 |
A p-[18F]fluoroethoxyphenyl bicyclic nucleoside analogue as a potential positron emission tomography imaging agent for varicella-zoster virus thymidine kinase gene expression. |
Institute For Medical Research |
| 17298046 |
12 |
Synthesis and preliminary evaluation of 18F- or 11C-labeled bicyclic nucleoside analogues as potential probes for imaging varicella-zoster virus thymidine kinase gene expression using positron emission tomography. |
Ku Leuven |
| 12941326 |
26 |
Improving the selectivity of acyclic nucleoside analogues as inhibitors of human mitochondrial thymidine kinase: replacement of a triphenylmethoxy moiety with substituted amines and carboxamides. |
Instituto De QuíMica MéDica (Csic) |
| 7837239 |
36 |
Synthesis, properties, and pharmacokinetic studies of N2-phenylguanine derivatives as inhibitors of herpes simplex virus thymidine kinases. |
University of Massachusetts Medical School |
| 6259353 |
4 |
Synthesis and antiviral activity of 1-(2-deoxy-beta-D-ribofuranosyl)-5-(methylmercapto)-2-pyrimidinone. |
TBA |
| 3033247 |
1 |
Synthesis and biological activity of unsaturated carboacyclic purine nucleoside analogues. |
TBA |
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