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Peter C. Tyler

Researcher Next ID · RN-042906

Researcher · Biochemistry, Genetics and Molecular Biology

Victoria University of Wellington

Wellington, New Zealand

Accepting doctoral researchersFunding unknown
Works count
313
Citation count
6,644
H-index
49
i10-index
128

Research interests

Biochemistry, Genetics and Molecular Biology
Chemistry
Medicine
Biochemical and Molecular Research
Carbohydrate Chemistry and Synthesis
HIV/AIDS drug development and treatment
Adenosine and Purinergic Signaling
Glycosylation and Glycoproteins Research

Publications

  • Synthesis of a Targeted Library of Heparan Sulfate Hexa‐ to Dodecasaccharides as Inhibitors of β‐Secretase: Potential Therapeutics for Alzheimer’s Disease

    Chemistry - A European Journal · 2013 · 10.1002/chem.201204519

  • Four generations of transition-state analogues for human purine nucleoside phosphorylase

    Proceedings of the National Academy of Sciences · 2010 · 10.1073/pnas.0913439107

  • Azetidine Based Transition State Analogue Inhibitors of N-Ribosyl Hydrolases and Phosphorylases

    Journal of Medicinal Chemistry · 2008 · https://doi.org/10.1021/jm701265n

  • Mannosylated liposomes as antigen delivery vehicles for targeting to dendritic cells

    Journal of Pharmacy and Pharmacology · 2006 · 10.1211/jpp.58.6.0003

  • Femtomolar Transition State Analogue Inhibitors of 5′-Methylthioadenosine/S-Adenosylhomocysteine Nucleosidase from Escherichia coli

    Journal of Biological Chemistry · 2005 · https://doi.org/10.1074/jbc.m414472200

  • Targeting a Novel Plasmodium falciparum Purine Recycling Pathway with Specific Immucillins

    Journal of Biological Chemistry · 2004 · https://doi.org/10.1074/jbc.m412693200

  • Plasmodium falciparum Purine Nucleoside Phosphorylase

    Journal of Biological Chemistry · 2004 · https://doi.org/10.1074/jbc.c400068200

  • Achieving the Ultimate Physiological Goal in Transition State Analogue Inhibitors for Purine Nucleoside Phosphorylase

    Journal of Biological Chemistry · 2003 · https://doi.org/10.1074/jbc.c300259200

  • Liposomal delivery of antigen to human dendritic cells

    Vaccine · 2003 · https://doi.org/10.1016/s0264-410x(02)00536-4

  • Exploring Structure−Activity Relationships of Transition State Analogues of Human Purine Nucleoside Phosphorylase

    Journal of Medicinal Chemistry · 2003 · 10.1021/jm030145r

  • Synthesis of Second-Generation Transition State Analogues of Human Purine Nucleoside Phosphorylase

    Journal of Medicinal Chemistry · 2003 · https://doi.org/10.1021/jm030305z

  • Transition State Analogue Inhibitors of Purine Nucleoside Phosphorylase from Plasmodium falciparum

    Journal of Biological Chemistry · 2002 · https://doi.org/10.1074/jbc.m105905200

  • Purine-less Death in Plasmodium falciparumInduced by Immucillin-H, a Transition State Analogue of Purine Nucleoside Phosphorylase

    Journal of Biological Chemistry · 2002 · https://doi.org/10.1074/jbc.m105906200

  • Addition of Lithiated 9-Deazapurine Derivatives to a Carbohydrate Cyclic Imine: Convergent Synthesis of the Aza-C-nucleoside Immucillins

    The Journal of Organic Chemistry · 2001 · https://doi.org/10.1021/jo0155613

  • Immucillin H, a powerful transition-state analog inhibitor of purine nucleoside phosphorylase, selectively inhibits human T lymphocytes

    Proceedings of the National Academy of Sciences · 2001 · https://doi.org/10.1073/pnas.071050798

  • Synthesis of Transition State Analogue Inhibitors for Purine Nucleoside Phosphorylase and N-Riboside Hydrolases

    Tetrahedron · 2000 · 10.1016/s0040-4020(00)00194-0

  • Transition State Structure of Purine Nucleoside Phosphorylase and Principles of Atomic Motion in Enzymatic Catalysis,

    Biochemistry · 2000 · https://doi.org/10.1021/bi002499f

  • Transition-state analogs as inhibitors of human and malarial hypoxanthine-guanine phosphoribosyltransferases.

    Nature Structural Biology · 1999 · https://doi.org/10.1038/9367

  • The 2.0 A structure of human hypoxanthine-guanine phosphoribosyltransferase in complex with a transition-state analog inhibitor.

    Nature Structural Biology · 1999 · https://doi.org/10.1038/9376

  • The 2.0 Å Structure of Malarial Purine Phosphoribosyltransferase in Complex with a Transition-State Analogue Inhibitor ,

    Biochemistry · 1999 · https://doi.org/10.1021/bi990664p

  • Prostaglandin E2-bisphosphonate conjugates: potential agents for treatment of osteoporosis

    Bioorganic & Medicinal Chemistry · 1999 · https://doi.org/10.1016/s0968-0896(99)00045-0

  • One-Third-the-Sites Transition-State Inhibitors for Purine Nucleoside Phosphorylase

    Biochemistry · 1998 · https://doi.org/10.1021/bi980658d

Current projects

    No projects listed.