Show
Sort by
-
- Journal Article
- A1
- open access
Synthesis and biological evaluation of cyclopropyl analogues of fosmidomycin as potent Plasmodium falciparum growth inhibitors
-
- Journal Article
- A1
- open access
2-Triazole-substituted adenosines: a new class of selective A₃ adenosine receptor agonists, partial agonists, and antagonists
-
Orthogonal activation of the reengineered A(3) adenosine receptor (neoceptor) using tailored nucleoside agonists
-
In vitro and in vivo anti-leishmanial activity of triterpenoid saponins isolated from Maesa balansae and some chemical derivatives
-
- Journal Article
- A1
- open access
Discovery of bicyclic thymidine analogues as selective and high-affinity inhibitors of Mycobacterium tuberculosis thymidine monophosphate kinase
-
- Journal Article
- A1
- open access
3'-C-branched-chain-substituted nucleosides and nucleotides as potent inhibitors of Mycobacterium tuberculosis thymidine monophosphate kinase
-
Modeling the adenosine receptors: Comparison of the binding domains of A(2A) agonists and antagonists
-
5 '-Deoxy congeners of 9-(3-amido-3-deoxy-beta-D-xylofuranosyl)-N-6-cyclopentyladenine: New adenosine A(1) receptor antagonists and inverse agonists.
-
Neoceptor concept based on molecular complementarity in GPCRs: A mutant adenosine A(3) receptor with selectively enhanced affinity for amine-modified nucleosides.
-
Experimental precedent for the need to involve the primary hydration layer of DNA in lead drug design.