11 articles for G Reiser
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Identification of Highly Promising Antioxidants/Neuroprotectants Based on Nucleoside 5'-Phosphorothioate Scaffold. Synthesis, Activity, and Mechanisms of Action.

Bar-Ilan University
Highly potent and selective ectonucleotide pyrophosphatase/phosphodiesterase I inhibitors based on an adenosine 5'-(a or¿)-thio-(a,ß- orß,¿)-methylenetriphosphate scaffold.

Bar-Ilan University
Highly efficient biocompatible neuroprotectants with dual activity as antioxidants and P2Y receptor agonists.

Bar-Ilan University
UDP made a highly promising stable, potent, and selective P2Y6-receptor agonist upon introduction of a boranophosphate moiety.

Bar-Ilan University
5-OMe-UDP is a potent and selective P2Y(6)-receptor agonist.

Bar-Ilan University
Diadenosine and diuridine poly(borano)phosphate analogues: synthesis, chemical and enzymatic stability, and activity at P2Y1 and P2Y2 receptors.

Bar-Ilan University
Molecular recognition in purinergic receptors. 2. Diastereoselectivity of the h-P2Y1-receptor.

Bar-Ilan University
Adenosine 5'-O-(1-boranotriphosphate) derivatives as novel P2Y(1) receptor agonists.

Bar-Ilan University
Molecular recognition of modified adenine nucleotides by the P2Y(1)-receptor. 1. A synthetic, biochemical, and NMR approach.

Bar-Ilan University
Diadenosine 5',5''-(boranated)polyphosphonate analogues as selective nucleotide pyrophosphatase/phosphodiesterase inhibitors.

Bar-Ilan University
Enzyme-assisted total synthesis of the optical antipodes D-myo-inositol 3,4,5-trisphosphate and D-myo-inositol 1,5, 6-trisphosphate: aspects of their structure-activity relationship to biologically active inositol phosphates.

Bergische UniversitäT Wuppertal