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Peter M Fischer
Peter M Fischer
Professor of Medicinal Chemistry, University of Nottingham
Verified email at nottingham.ac.uk - Homepage
Title
Cited by
Cited by
Year
Untangling tau hyperphosphorylation in drug design for neurodegenerative diseases
MP Mazanetz, PM Fischer
Nature reviews Drug discovery 6 (6), 464-479, 2007
6302007
Oral treatment targeting the unfolded protein response prevents neurodegeneration and clinical disease in prion-infected mice
JA Moreno, M Halliday, C Molloy, H Radford, N Verity, JM Axten, CA Ortori, ...
Science translational medicine 5 (206), 206ra138-206ra138, 2013
6272013
In vitro and in vivo antitumor properties of the cyclin dependent kinase inhibitor CYC202 (R‐roscovitine)
SJ McClue, D Blake, R Clarke, A Cowan, L Cummings, PM Fischer, ...
International journal of cancer 102 (5), 463-468, 2002
4772002
Partial restoration of protein synthesis rates by the small molecule ISRIB prevents neurodegeneration without pancreatic toxicity
M Halliday, H Radford, Y Sekine, J Moreno, N Verity, J Le Quesne, ...
Cell death & disease 6 (3), e1672-e1672, 2015
3342015
Cyclin-dependent kinase 9: a key transcriptional regulator and potential drug target in oncology, virology and cardiology
S Wang, PM Fischer
Trends in pharmacological sciences 29 (6), 302-313, 2008
2932008
Inhibitors of cyclin-dependent kinases as anti-cancer therapeutics
PM Fischer, DP Lane
Current medicinal chemistry 7 (12), 1213-1245, 2000
2672000
Diketopiperazines in peptide and combinatorial chemistry
PM Fischer
Journal of peptide science: an official publication of the European Peptide …, 2003
2522003
Mutations in a translation initiation factor identify the target of a memory-enhancing compound
Y Sekine, A Zyryanova, A Crespillo-Casado, PM Fischer, HP Harding, ...
Science 348 (6238), 1027-1030, 2015
2292015
Structure–activity relationship of truncated and substituted analogues of the intracellular delivery vector Penetratin
PM Fischer, NZ Zhelev, S Wang, JE Melville, R Fåhraeus, DP Lane
The Journal of peptide research 55 (2), 163-172, 2000
2212000
4-Arylazo-3,5-diamino-1H-pyrazole CDK Inhibitors:  SAR Study, Crystal Structure in Complex with CDK2, Selectivity, and Cellular Effects
V Kryštof, P Cankař, I Fryšová, J Slouka, G Kontopidis, P Džubák, ...
Journal of medicinal chemistry 49 (22), 6500-6509, 2006
2202006
Cellular delivery of impermeable effector molecules in the form of conjugates with peptides capable of mediating membrane translocation
PM Fischer, E Krausz, DP Lane
Bioconjugate chemistry 12 (6), 825-841, 2001
2012001
2-Anilino-4-(thiazol-5-yl) pyrimidine CDK inhibitors: synthesis, SAR analysis, X-ray crystallography, and biological activity
S Wang, C Meades, G Wood, A Osnowski, S Anderson, R Yuill, M Thomas, ...
Journal of medicinal chemistry 47 (7), 1662-1675, 2004
1972004
CDK inhibitors in clinical development for the treatment of cancer
PM Fischer, A Gianella-Borradori
Expert opinion on investigational drugs 12 (6), 955-970, 2003
1872003
The design, synthesis and application of stereochemical and directional peptide isomers: a critical review
PM Fischer
Current Protein and Peptide Science 4 (5), 339-356, 2003
1862003
Binding of ISRIB reveals a regulatory site in the nucleotide exchange factor eIF2B
AF Zyryanova, F Weis, A Faille, AA Alard, A Crespillo-Casado, Y Sekine, ...
Science 359 (6383), 1533-1536, 2018
1852018
Structure of free MDM2 N-terminal domain reveals conformational adjustments that accompany p53-binding
S Uhrinova, D Uhrin, H Powers, K Watt, D Zheleva, P Fischer, C McInnes, ...
Journal of molecular biology 350 (3), 587-598, 2005
1842005
Recent progress in the discovery and development of cyclin-dependent kinase inhibitors
PM Fischer, A Gianella-Borradori
Expert opinion on investigational drugs 14 (4), 457-477, 2005
1812005
Dietary fats and pharmaceutical lipid excipients increase systemic exposure to orally administered cannabis and cannabis-based medicines
A Zgair, JCM Wong, JB Lee, J Mistry, O Sivak, KM Wasan, IM Hennig, ...
American journal of translational research 8 (8), 3448, 2016
1632016
The design of drug candidate molecules as selective inhibitors of therapeutically relevant protein kinases
PM Fischer
Current medicinal chemistry 11 (12), 1563-1583, 2004
1602004
Discovery of a novel family of CDK inhibitors with the program LIDAEUS: structural basis for ligand-induced disordering of the activation loop
SY Wu, I McNae, G Kontopidis, SJ McClue, C McInnes, KJ Stewart, ...
Structure 11 (4), 399-410, 2003
1602003
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