Universität Wien

320003 VO Biophysical Pharmaceutical Chemistry (2014W)

4.00 ECTS (2.00 SWS), SPL 32 - Pharmazie

ACHTUNG: Vorlesungsbeginn: 13.11.2014, 10.30 Uhr, HS 4

Prüfungstermine:

Stoffsemester WS14
24.03.2015 15.00 Uhr HS 6
22.04.2015 11.30 Uhr HS 6
28.05.2015 09.45 Uhr HS 6
18.06.2015 13.15 Uhr HS 6

Stoffsemester WS 2014:

27.01.2015 13.00 Uhr HS 6
11.02.2015 12.00 Uhr HS 7
25.02.2015 12.00 Uhr HS 7

Moodle

Details

Language: German

Examination dates

Lecturers

Classes (iCal) - next class is marked with N

  • Thursday 06.11. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Thursday 13.11. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Thursday 20.11. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Thursday 27.11. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Tuesday 02.12. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Thursday 04.12. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Tuesday 09.12. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Thursday 11.12. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Tuesday 16.12. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Thursday 18.12. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Thursday 08.01. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Tuesday 13.01. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Thursday 15.01. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Tuesday 20.01. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Thursday 22.01. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG
  • Tuesday 27.01. 10:30 - 12:00 UZA2 Hörsaal 4 (Raum 2Z221) 2.OG

Information

Aims, contents and method of the course

the thermodynamic basis for interaction of drugs with biomolecules; interaction forces involved in drug-biomolecule interaction (ionic-, dipol-dipol-, electronendonor/acceptor-, hydrophobic-, Van der Waals-interactions, hydrogen bonding) and methods to measure these forces (microcalorimetrie, ORCD, binding studies), determination of the structure of ligand-protein complexes (X-ray crystallography, NMR-spectroscopy), strategies for identification of lead-compounds (serendipity, transition state mimicry, high throughput screening, in silico screening), optimisation of lead compounds - rational drug design (statistical background, 2D- and 3D- structure activity relationship analysis, methods used in quantitative structure activity relationship studies), structure based design (docking, SAR by NMR, de novo design)

Assessment and permitted materials

Written exam, 12 questions, 100 points, 90 minutes

Minimum requirements and assessment criteria

The lecture gives an overview on the theoretical background and the experimental biophysical methods for the rational design of new drugs. Main topics are the molecular basis of drug-receptor interaction, methods for measuring the corresponding interaction forces and the use of these data in computational drug design.

Examination topics

Language: German (material partly in English); powerpoint presentation, software demonstrations

Reading list

Association in the course directory

A210

Last modified: Sa 02.04.2022 00:27