Charles University Faculty of Pharmacy in Hradec Králové Department of Pharmacology and Toxicology Student: Anna Odvárková Supervisor: RNDr. Jakub Hofman, Ph.D. Consultants: Carina Lemke Prof. Dr. Michael Gütschow Title of diploma thesis: Kinetic Evaluation of Potential Inhibitors for Selected Cysteine Proteases Cysteine cathepsins are proteases which are naturally present in the human body, taking part in various physiological processes such as cell signaling, proliferation or bone remodeling. However, their dysregulation leads to serious disorders. An aberrant activity of cysteine cathepsins is present in diseases like cancer, osteoporosis, neurodegenerative disorders or autoimmune diseases. Therefore, these enzymes can serve as valuable ...
This dissertation thesis focuses on creating tools for the analysis and potential therapeutic interv...
Cysteine proteases are important drug targets due to their involvement in many biological processes ...
Gold compounds form a new class of promising metal-based drugs with a number of potential therapeuti...
IN ENGLISH Charles University Faculty of Pharmacy in Hradec Králové Department of Biological and Med...
IN ENGLISH Charles University Faculty of Pharmacy in Hradec Králové Department of Biological and Med...
Proteases are enzymes that catalyze the hydrolysis of amide bonds in peptides and proteins. Due to ...
Rhodesain (RD) is a parasitic, human cathepsin L (hCatL) like cysteine protease produced by Trypanos...
Human African Trypanosomiasis (HAT) is an endemic parasitic disease of sub-Saharan Africa, caused by...
The targeting of parasite cysteine proteases with small molecules is emerging as a possible approach...
Human cathepsins L and K are cysteine proteases that play important roles in physiological and patho...
The targeting of parasite cysteine proteases with small molecules is emerging as a possible approach...
Ziel der Dissertation „Entwicklung von Cysteinproteaseinhibitoren – ein klassischer und ein kombinat...
This dissertation thesis focuses on creating tools for the analysis and potential therapeutic interv...
Rhodesain (RD) is a parasitic, human cathepsin L (hCatL) like cysteine protease produced by Trypanos...
This dissertation thesis focuses on creating tools for the analysis and potential therapeutic interv...
This dissertation thesis focuses on creating tools for the analysis and potential therapeutic interv...
Cysteine proteases are important drug targets due to their involvement in many biological processes ...
Gold compounds form a new class of promising metal-based drugs with a number of potential therapeuti...
IN ENGLISH Charles University Faculty of Pharmacy in Hradec Králové Department of Biological and Med...
IN ENGLISH Charles University Faculty of Pharmacy in Hradec Králové Department of Biological and Med...
Proteases are enzymes that catalyze the hydrolysis of amide bonds in peptides and proteins. Due to ...
Rhodesain (RD) is a parasitic, human cathepsin L (hCatL) like cysteine protease produced by Trypanos...
Human African Trypanosomiasis (HAT) is an endemic parasitic disease of sub-Saharan Africa, caused by...
The targeting of parasite cysteine proteases with small molecules is emerging as a possible approach...
Human cathepsins L and K are cysteine proteases that play important roles in physiological and patho...
The targeting of parasite cysteine proteases with small molecules is emerging as a possible approach...
Ziel der Dissertation „Entwicklung von Cysteinproteaseinhibitoren – ein klassischer und ein kombinat...
This dissertation thesis focuses on creating tools for the analysis and potential therapeutic interv...
Rhodesain (RD) is a parasitic, human cathepsin L (hCatL) like cysteine protease produced by Trypanos...
This dissertation thesis focuses on creating tools for the analysis and potential therapeutic interv...
This dissertation thesis focuses on creating tools for the analysis and potential therapeutic interv...
Cysteine proteases are important drug targets due to their involvement in many biological processes ...
Gold compounds form a new class of promising metal-based drugs with a number of potential therapeuti...