Code No: 13169/PCI
FACULTY OF PHARMACY
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M. Pharmacy (Pharmaceutical Chemistry) II-Semester (PCI) (Suppl.) Examination, February 2019
Subject: Computer Aided Drug Design
Time : 3 Hrs Max. Marks: 75
Note: Answer any Five questions. All questions carry equal marks
- a) What is QSAR? Describe the physicochemical parameters used in QSAR.
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b) Explain how hydrophobicity constant and Hammet constants of a substituent are measured experimentally? (10+5) - a) Discuss in detail about Hansch analysis and its applications.
b) Write a note on 3D QSAR studies. (9+6) - a) What is quantum mechanics? Describe the use of quantum mechanics in drug design.
b) What is molecular docking? Discuss the general method of molecular docking. (8+7) - a) Describe the steps involved in Homology modeling of a protein. (8+7)
b) Discuss the concept of predicting ADMET properties and its importance in drug design. - a) What is known as pharmacophore? Discuss the concept of Pharmacophore based virtual screening.
b) Write a note on Similarity based Virtual screening (8+7) - a) Write a note on Scoring techniques in Molecular docking.
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b) Write a note on Fragment based drug design. (7+8) - a) What is virtual screening? Enumerate various virtual screening techniques
b) Write a note on Privileged structures. (8+7) - a) Discuss the importance of molecular Mechanics in drug design.
b) What is Free Wilson analysis? What are the advantages and disadvantages over hansch analysis?
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