Code No. 13325/PCI
FACULTY OF PHARMACY
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M. Pharmacy (Pharmaceutical Chemistry) II-Semester (PCI) (Main) Examination, August 2019
Subject: Computer Aided Drug Design
Time: 3 Hrs Max. Marks: 75
Note: Answer any five questions. All questions carry equal marks.
- (a) Discuss in detail about various parameters used in QSAR.
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(b) How is substituent hydrophobicity constant used in QSAR? Discuss with an example equation. (10+5) - (a) What is Hansch analysis and discuss how it is used in predicting the biological activity?
(b) Give the advantages and disadvantages of Hansch analysis. (9+6) - (a) What is quantum mechanics? Describe the use of quantum mechanics in drug design.
(b) What is molecular docking? Discuss the steps involved in molecular docking? (8+7) - (a) What is Homology modeling? Discuss its importance in drug design. (8+7)
(b) Write a note on fragment based drug design. - (a) What is known as pharmacophore? Discuss the concept of Pharmacophore based virtual screening.
(b) Write a note on pharmacophore modeling. (8+7) - (a) Write a note on Scoring techniques in Molecular docking.
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(b) Discuss various models for predicting ADMET properties. (7+8) - (a) What is virtual screening? Discuss about druglikeness screening.
(b) Write a note on Privileged structures. (8+7) - (a) What is bioactive conformation? Discuss various energy minimization techniques. (8+7)
(b) Write a note on application of Free Wilson analysis in drug design.
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