Universität Wien

323109 VU Drug targets, hit discovery and case studies - MPS5 (2018S)

2.00 ECTS (1.00 SWS), SPL 32 - Pharmazie
Continuous assessment of course work

Details

Language: English

Lecturers

Classes

Currently no class schedule is known.

Information

Aims, contents and method of the course

The course aims to provide students with an understanding of the thermodynamics of protein-ligand interaction and the contribution of the entropic term, the importance of drug like properties in drug discovery and strategies for identifying and validating new targets. These topics will be discussed on specific case studies concerning discovery of new medicines targeting nuclear receptors, kinases and proteases.
 Protein structure, Protein-ligand interactions (thermodynamics of the interaction, free energy, enthalpy, entropy).
 structure and function, physicochemical properties, lead-like properties, QSAR
 Target identification and validation: biochemical, pharmacological and genomic methodologies, (genetic engineering, transgenic animals, silencing genes, recombinant proteins, transcriptomics proteomics)
 Case studies in drug discovery. (nuclear receptors, kinases, proteases)

Assessment and permitted materials

One term paper on a drug target
A written examination on approaches to analog design (on June 26th)

Minimum requirements and assessment criteria

Examination topics

Reading list

• Basic Principles of Drug Discovery and Development by Benjamin Blass, Academic Press
• Drug Discovery and Development by Raymond Hill, Churchill Livingstone Elsevier
• Drug Design by Gerhardt Klebe, Springer
• Drug like properties: Concepts, Structure design and Methods by Edward H. Kerns and Li Di, Academic Press Elsevier

Association in the course directory

Last modified: Fr 31.08.2018 08:43