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Orthogonal activation of the reengineered A(3) adenosine receptor (neoceptor) using tailored nucleoside agonists
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- Journal Article
- A1
- open access
Exploring human adenosine A₃ receptor complementarity and activity for adenosine analogues modified in the ribose and purine moiety
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Neoceptor concept applied to human A2A and A3 adenosine receptors.
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- PhD Thesis
- open access
Synthesis and Biological Evaluation of Modified Adenosine and Thymidine Nucleoside Analogues
(2004) -
Modulation of adenosine receptor affinity and intrinsic efficacy in adenine nucleosides substituted at the 2-position
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Design of a neoceptor and complementary neoligand derived from the A2A adenosine receptor.
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Presence of N,N-Dimethyl-3,4-Methylenedioxyamphetamine(MDDM) in a fatal MDMA-overdose
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- Journal Article
- A1
- open access
Mycobacterium tuberculosis thymidine monophosphate kinase inhibitors: Biological evaluation and conformational analysis of 2 '- and 3 '-modified thymidine analogues
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Thymidine and thymidine-5 '-O-monophosphate analogues as inhibitors of Mycobacterium tuberculosis thymidylate kinase
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Modeling the adenosine receptors: Comparison of the binding domains of A(2A) agonists and antagonists
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Amine-modified nucleosides as adenosine A(3) neoceptor ligands
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Thymidine (monophosphate) analogues as Mycobacterium tuberculosis thymidylate kinase inhibitors
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Chemotaxonomic features associated with flavonoids of cannabinoid-free cannabis (Cannabis sativa subsp sativa L.) in relation to hops (Humulus lupulus L.).
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Neoceptor concept based on molecular complementarity in GPCRs: A mutant adenosine A(3) receptor with selectively enhanced affinity for amine-modified nucleosides.