Search Results - "Shanks, Emma J."
-
1
One Scaffold, Three Binding Modes: Novel and Selective Pteridine Reductase 1 Inhibitors Derived from Fragment Hits Discovered by Virtual Screening
Published in Journal of medicinal chemistry (23-07-2009)“…The enzyme pteridine reductase 1 (PTR1) is a potential target for new compounds to treat human African trypanosomiasis. A virtual screening campaign for…”
Get full text
Journal Article -
2
Strategic siRNA screening approaches to target cancer at the Cancer Research UK Beatson Institute
Published in Combinatorial chemistry & high throughput screening (01-05-2014)“…The RNAi Screening Facility at the Cancer Research UK Beatson Institute combines siRNA genome-wide screening with drug screening coupled with High Content…”
Get more information
Journal Article -
3
Investigation of Trypanothione Reductase as a Drug Target in Trypanosoma brucei
Published in ChemMedChem (07-12-2009)“…There is an urgent need for new drugs for the treatment of tropical parasitic diseases such as human African trypanosomiasis, which is caused by Trypanosoma…”
Get full text
Journal Article -
4
Synthesis and Evaluation of 1-(1-(Benzo[b]thiophen-2-yl)cyclohexyl)piperidine (BTCP) Analogues as Inhibitors of Trypanothione Reductase
Published in ChemMedChem (03-08-2009)“…Thirty two analogues of phencyclidine were synthesised and tested as inhibitors of trypanothione reductase (TryR), a potential drug target in trypanosome and…”
Get full text
Journal Article -
5
3q26‐29 Amplification in head and neck squamous cell carcinoma: a review of established and prospective oncogenes
Published in The FEBS journal (01-09-2017)“…Head and neck squamous cell carcinoma (HNSCC) is significantly underrepresented in worldwide cancer research, yet survival rates for the disease have remained…”
Get full text
Journal Article -
6
Dihydroquinazolines as a Novel Class of Trypanosoma brucei Trypanothione Reductase Inhibitors: Discovery, Synthesis, and Characterization of their Binding Mode by Protein Crystallography
Published in Journal of medicinal chemistry (13-10-2011)“…Trypanothione reductase (TryR) is a genetically validated drug target in the parasite Trypanosoma brucei, the causative agent of human African trypanosomiasis…”
Get full text
Journal Article -
7
The High-Affinity Interaction between ORC and DNA that Is Required for Replication Licensing Is Inhibited by 2-Arylquinolin-4-Amines
Published in Cell chemical biology (17-08-2017)“…In late mitosis and G , origins of DNA replication must be "licensed" for use in the upcoming S phase by being encircled by double hexamers of the…”
Get more information
Journal Article -
8
Development and validation of a cytochrome c-coupled assay for pteridine reductase 1 and dihydrofolate reductase
Published in Analytical biochemistry (15-01-2010)“…Activity of the pterin- and folate-salvaging enzymes pteridine reductase 1 (PTR1) and dihydrofolate reductase–thymidylate synthetase (DHFR-TS) is commonly…”
Get full text
Journal Article -
9
Design, Synthesis and Biological Evaluation of Novel Inhibitors of Trypanosoma brucei Pteridine Reductase 1
Published in ChemMedChem (07-02-2011)“…Genetic studies indicate that the enzyme pteridine reductase 1 (PTR1) is essential for the survival of the protozoan parasite Trypanosoma brucei. Herein, we…”
Get full text
Journal Article -
10
Cover Picture: Improved Tricyclic Inhibitors of Trypanothione Reductase by Screening and Chemical Synthesis / Synthesis and Evaluation of 1-(1-(Benzo[b]thiophen-2-yl)cyclohexyl)piperidine (BTCP) Analogues as Inhibitors of Trypanothione Reductase (ChemMedChem 8/2009)
Published in ChemMedChem (03-08-2009)Get full text
Journal Article -
11
Cover Picture: Synthesis and Evaluation of Indatraline-Based Inhibitors for Trypanothione Reductase / Design, Synthesis and Biological Evaluation of Novel Inhibitors of Trypanosoma brucei Pteridine Reductase 1 / Modified 5′-Trityl Nucleosides as Inhibitors of Plasmodium falciparum dUTPase (ChemMedChem 2/2011)
Published in ChemMedChem (07-02-2011)Get full text
Journal Article