sesone has been researched along with 6-amino-5-bromouracil in 10 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (10.00) | 18.2507 |
2000's | 6 (60.00) | 29.6817 |
2010's | 3 (30.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Balzarini, J; Camarasa, MJ; De Clercq, E; Esnouf, R; Esteban-Gamboa, A; Pérez-Pérez, MJ | 1 |
Bryce, RA; Douglas, KT; Freeman, S; Gbaj, A; Jaffar, M; McNally, VA; Stratford, IJ | 1 |
Chinje, E; Douglas, KT; Freeman, S; Gbaj, A; Reigan, P; Stratford, IJ | 1 |
Ashton, SE; Barry, ST; Bryce, RA; Cole, C; Douglas, KT; Edwards, PN; Freeman, S; Gbaj, A; Jaffar, M; Luke, RW; Page, KM; Reigan, P; Stratford, IJ | 1 |
Bryce, RA; Freeman, S; Gbaj, A; Reigan, P; Stratford, IJ | 1 |
Bera, H; Chiu, GN; Chui, WK; Dolzhenko, AV; Li, J; Sun, L | 1 |
Bera, H; Chigurupati, S | 1 |
Basso, LA; Bergo, P; Campos, MM; da Silva Dadda, A; de Moura Sperotto, ND; Deves Roth, C; Duarte de Souza, AP; Ev Neves, C; Freitas de Freitas, T; Machado, P; Moura, S; Reisdorfer Paula, F; Rodrigues-Junior, VS; Santos, DS; Souza Macchi, F; Valim Bizarro, C | 1 |
Balzarini, J; Camarasa, MJ; De Clercq, E; Esnouf, R; Gamboa, AE; Liekens, S; Neyts, J; Pérez-Pérez, MJ | 1 |
Balzarini, J; Camarasa, MJ; De Clercq, E; Degrève, B; Engelborghs, Y; Esnouf, R; Esteban-Gamboa, A; Pérez-Pérez, MJ | 1 |
1 review(s) available for sesone and 6-amino-5-bromouracil
Article | Year |
---|---|
Recent discovery of non-nucleobase thymidine phosphorylase inhibitors targeting cancer.
Topics: Animals; Antineoplastic Agents; Carcinogenesis; Drug Discovery; Enzyme Inhibitors; Humans; Neoplasms; Thymidine Phosphorylase | 2016 |
9 other study(ies) available for sesone and 6-amino-5-bromouracil
Article | Year |
---|---|
Design, synthesis, and enzymatic evaluation of multisubstrate analogue inhibitors of Escherichia coli thymidine phosphorylase.
Topics: Chromatography, High Pressure Liquid; Drug Design; Enzyme Inhibitors; Escherichia coli; Kinetics; Models, Molecular; Organophosphonates; Pyrimidinones; Structure-Activity Relationship; Substrate Specificity; Thymidine; Thymidine Phosphorylase; Uracil | 2000 |
Identification of a novel class of inhibitor of human and Escherichia coli thymidine phosphorylase by in silico screening.
Topics: Binding Sites; Computer Simulation; Crystallography, X-Ray; Databases, Genetic; Drug Design; Drug Evaluation, Preclinical; Enzyme Inhibitors; Escherichia coli; Humans; Hydrazines; Imidazoles; Kinetics; Models, Molecular; Recombinant Proteins; Structure-Activity Relationship; Thymidine; Thymidine Phosphorylase | 2003 |
Synthesis and enzymatic evaluation of xanthine oxidase-activated prodrugs based on inhibitors of thymidine phosphorylase.
Topics: Antineoplastic Agents; Escherichia coli; Humans; Prodrugs; Pyrimidines; Pyrroles; Pyrrolidines; Thymidine Phosphorylase; Xanthine Oxidase | 2004 |
Aminoimidazolylmethyluracil analogues as potent inhibitors of thymidine phosphorylase and their bioreductive nitroimidazolyl prodrugs.
Topics: Animals; Antineoplastic Agents; Binding Sites; Biological Availability; Escherichia coli; Humans; Imidazoles; Mice; Models, Molecular; Nitroimidazoles; Oxidation-Reduction; Prodrugs; Structure-Activity Relationship; Thymidine Phosphorylase; Uracil | 2005 |
Xanthine oxidase-activated prodrugs of thymidine phosphorylase inhibitors.
Topics: Enzyme Activation; Enzyme Inhibitors; Humans; Magnetic Resonance Spectroscopy; Models, Molecular; Prodrugs; Spectrophotometry, Infrared; Thymidine Phosphorylase; Xanthine Oxidase | 2008 |
Fragment-based approach to the design of 5-chlorouracil-linked-pyrazolo[1,5-a][1,3,5]triazines as thymidine phosphorylase inhibitors.
Topics: Dose-Response Relationship, Drug; Drug Design; Enzyme Inhibitors; Humans; Molecular Structure; Pyrazines; Structure-Activity Relationship; Thymidine Phosphorylase; Triazines; Uracil | 2013 |
Design of Novel Inhibitors of Human Thymidine Phosphorylase: Synthesis, Enzyme Inhibition, in Vitro Toxicity, and Impact on Human Glioblastoma Cancer.
Topics: Animals; Area Under Curve; Brain Neoplasms; Cell Line; Cell Line, Tumor; Drug Design; Enzyme Inhibitors; Glioblastoma; Half-Life; Humans; Thymidine Phosphorylase | 2019 |
7-Deazaxanthine, a novel prototype inhibitor of thymidine phosphorylase.
Topics: Allantois; Animals; Antibiotics, Antineoplastic; Binding Sites; Bromouracil; Chick Embryo; Chorion; Cyclohexanes; Dose-Response Relationship, Drug; Drug Design; Enzyme Inhibitors; Escherichia coli; Neovascularization, Physiologic; O-(Chloroacetylcarbamoyl)fumagillol; Sesquiterpenes; Thymidine; Thymidine Phosphorylase; Thymine; Xanthines | 1998 |
Kinetic analysis of novel multisubstrate analogue inhibitors of thymidine phosphorylase.
Topics: Bromouracil; Enzyme Inhibitors; Escherichia coli; Kinetics; Models, Molecular; Structure-Activity Relationship; Substrate Specificity; Thymidine; Thymidine Phosphorylase; Thymine; Xanthines | 2000 |