Rajahdaandhi University of Health Sciences
First Year M. Pharm Degree Examination - May 2016
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[Time: 3 Hours]
Medicinal Chemistry – I (Drug Design)
(Revised Scheme 4)
Q.P. CODE: 9347
Your answers should be specific to the questions asked.
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Draw neat, labeled diagrams wherever necessary.
[Max. Marks: 100]
LONG ESSAY (Answer any TWO) 2 X 20 = 40 Marks
- Explain various steps involved in developing a QSAR model and discuss the steric parameters used in a QSAR.
- a) Explain the rational design of non-covalent and covalent binding enzyme inhibitors. (12+8)
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b) Describe enzymes inhibitors as transition state analogs. - Write notes on:
a) Conformational analysis
b) Virtual screening
c) Aromatase inhibitors--- Content provided by FirstRanker.com ---
d) HIV-Protease inhibitor
SHORT ESSAY (Answer any FIVE) 5 X 10 = 50 Marks
- Discuss the design and development of prodrugs with two specific examples.
- Give an account of various protein-ligand docking techniques and their importance in drug discovery.
- Explain the different non-covalent forces involved in drug receptor interaction.
- Define the terms receptor, agonist, partial agonist and antagonist. Discuss drug-receptor interaction theories.
- With suitable examples, explain the applications of recombinant DNA technology in pharmacy.
- What is a lead molecule? Discuss the various stages involved in identification of a lead molecule.
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SHORT NOTES 2 X 5 = 10 Marks
- Write a note on development of t-PA as a therapeutic agents.
- What is epitope mapping? Give the importance of epitope mapping in drug design.
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