PMID

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Article Title

Organization

Tight binding enantiomers of pre-clinical drug candidates.

Victoria University of Wellington

Transition state analogue inhibitors of human methylthioadenosine phosphorylase and bacterial methylthioadenosine/S-adenosylhomocysteine nucleosidase incorporating acyclic ribooxacarbenium ion mimics.

Industrial Research

Second generation transition state analogue inhibitors of human 5'-methylthioadenosine phosphorylase.

Industrial Research

Targeting the polyamine pathway with transition-state analogue inhibitors of 5'-methylthioadenosine phosphorylase.

Industrial Research

Synthesis of a potent transition-state inhibitor of 5'-deoxy-5'-methylthioadenosine phosphorylase.

Biocryst Pharmaceuticals

Design and synthesis of potent"sulfur-free" transition state analogue inhibitors of 5'-methylthioadenosine nucleosidase and 5'-methylthioadenosine phosphorylase.

Industrial Research

Selective Inhibitors of Helicobacter pylori Methylthioadenosine Nucleosidase and Human Methylthioadenosine Phosphorylase.

Albert Einstein College of Medicine

Heat Capacity Changes for Transition-State Analogue Binding and Catalysis with Human 5'-Methylthioadenosine Phosphorylase.

Albert Einstein College of Medicine

Picomolar inhibitors as transition-state probes of 5'-methylthioadenosine nucleosidases.

Albert Einstein College of Medicine

Azetidine based transition state analogue inhibitors of N-ribosyl hydrolases and phosphorylases.

Industrial Research