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Biological and Pharmaceutical Bulletin, ISSN 0918-6158, 2011, Volume 34, Issue 1, pp. 173 - 176
Plasmodium falciparum thymidylate kinase (PfTMK) is a potential chemotherapeutic target as it can tolerate a range of substrates, which distinguishes it from... 
thymidylate kinase | isothermal titration calorimetry | plasmodium | Plasmodium | Thymidylate kinase | Isothermal titration calorimetry | PHARMACOLOGY & PHARMACY | FALCIPARUM | DRUG DISCOVERY | Plasmodium falciparum - enzymology | Protein Binding | Substrate Specificity | Animals | Nucleotides | Nucleoside-Phosphate Kinase - metabolism
Journal Article
Journal Article
ChemBioChem, ISSN 1439-4227, 07/2016, Volume 17, Issue 14, pp. 1291 - 1291
The cover picture shows the reduction‐responsive structural transition of an oligonucleotide bearing a newly designed chemically reactive nucleobase (G NB )... 
G-quadruplexes | stimuli-responsive | conjugation | DNA structures | cleavage reactions | Deoxyribonucleic acid--DNA
Journal Article
International Journal of Biological Macromolecules, ISSN 0141-8130, 02/2018, Volume 107, Issue Pt B, pp. 2566 - 2573
Journal Article
Chemistry Letters, ISSN 0366-7022, 8/2015, Volume 44, Issue 8, pp. 1137 - 1139
Herein, we describe how a peptide amphiphile, consisting of a pro-apoptotic peptide and a hydrophobic tail connected by a reduction-responsive cleavable... 
SMAC/DIABLO | CELLS | DESIGN | ACID | REDUCTION | STRUCTURAL BASIS | IN-VIVO | XIAP | HYPOXIA | BINDING | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Journal Article
Cancer Science, ISSN 1347-9032, 05/2018, Volume 109, Issue 5, pp. 1455 - 1467
Journal Article
ChemBioChem, ISSN 1439-4227, 07/2016, Volume 17, Issue 14, pp. 1304 - 1307
Journal Article
Chemistry Letters, ISSN 0366-7022, 01/2015, Volume 44, Issue 8, pp. 1137 - 1137
Herein, we describe how a peptide amphiphile, consisting of a pro-apoptotic peptide and a hydrophobic tail connected by a reduction-responsive cleavable... 
Peptides | Morphology | Nanostructure | Spacers
Journal Article
Tetrahedron, ISSN 0040-4020, 07/2016, Volume 72, Issue 27-28, pp. 4016 - 4021
A convenient method for the post-modification of any peptide bearing a disulfide bond via rapid ligand-free copper-catalyzed azide–alkyne cycloaddition (CuAAC)... 
Click chemistry | Peptides | Orthogonal techniques | Post-modification | CuAAC | HUISGEN CYCLOADDITION | LIGATION | CHEMISTRY, ORGANIC | PROTEINS | Esters | Drug discovery | Copper | Acetylene | Disulfides | Terminals | Bonding | Glutathione | Alkynes | Bearing
Journal Article
Biological & Pharmaceutical Bulletin, ISSN 0918-6158, 2011, Volume 34, Issue 1, pp. 173 - 176
Plasmodium falciparum thymidylate kinase (PfTMK) is a potential chemotherapeutic target as it can tolerate a range of substrates, which distinguishes it from... 
Journal Article
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 10/2018, Volume 28, Issue 19, pp. 3174 - 3176
Journal Article