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Download RGUHS M.Pharmacy First Year May 2016 9347 Medicinal Chemistry ? I Drug Design Revised Scheme 4 Question Paper

Download RGUHS (Rajiv Gandhi University of Health Sciences) M Pharma (Master of Pharmacy) First Year (1st Year) May 2016 9347 Medicinal Chemistry ? I Drug Design Revised Scheme 4 Question Paper.

This post was last modified on 20 December 2019

RGUHS M.Pharm Last 10 Years 2011-2021 Previous Question Papers || Rajiv Gandhi University of Health Sciences


Rajahdaandhi University of Health Sciences

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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

  1. Explain various steps involved in developing a QSAR model and discuss the steric parameters used in a QSAR.
  2. 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.
  3. Write notes on:
    a) Conformational analysis
    b) Virtual screening
    c) Aromatase inhibitors

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    d) HIV-Protease inhibitor

SHORT ESSAY (Answer any FIVE) 5 X 10 = 50 Marks

  1. Discuss the design and development of prodrugs with two specific examples.
  2. Give an account of various protein-ligand docking techniques and their importance in drug discovery.
  3. Explain the different non-covalent forces involved in drug receptor interaction.
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  5. Define the terms receptor, agonist, partial agonist and antagonist. Discuss drug-receptor interaction theories.
  6. With suitable examples, explain the applications of recombinant DNA technology in pharmacy.
  7. What is a lead molecule? Discuss the various stages involved in identification of a lead molecule.

SHORT NOTES 2 X 5 = 10 Marks

  1. Write a note on development of t-PA as a therapeutic agents.
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  3. What is epitope mapping? Give the importance of epitope mapping in drug design.

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