35182 : Medicinal Chemistry - IV : T-8.2
Pages : 1
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Time : Three Hours Max. Marks : 60
- All questions carry equal marks.
- Answer five questions.
- Discuss the reaction, mechanism wherever necessary.
- Use of pen Blue/Black ink/refill only for writing the answer book.
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- Explain in detail rational drug design. Give its advantages over conventional drug design. 12
- Lipophilicity, Shape and electron distribution have a major influence on drug activity. 12 Explain the parameters that are commonly used as measure of these properties in QSAR approach to drug design.
- What is QSAR? Explain Hansch analysis and Topliss decision tree methods in QSAR approach to drug design. 12
- Write a detail account on structure based drug design with examples. 12
- Explain in detail concept of genetic engineering. Give its merits and demerits. 12
- What do you understand by Design of ligand? Explain ligand design based on 3D structure of receptor. 12
- Write a note on any two. 12
- Gene therapy.
- Molecular mechanics.
- Lead identification.
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This download link is referred from the post: SGBAU B.Pharm Last 10 Years 2010-2020 Question Papers || Sant Gadge Baba Amravati university
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