Computer Aided Drug Design (BP807ET) - AKTU Question Paper 2024-25
B.Pharm · Semester 8 · Free PDF Download
This is the official AKTU Computer Aided Drug Design Previous Year Question Paper for B.Pharm Semester 8, academic session 2024-25. Published by Dr. A.P.J. Abdul Kalam Technical University (AKTU/UPTU), Lucknow. Free PDF download — no login required.
Course:B.Pharm
Semester:Semester 8
Session:2024-25
University:AKTU / UPTU
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Questions Asked in 2024-25
Computer Aided Drug Design (BP807ET) — complete question paper · 75 marks · 3 Hours
Section BAttempt any two parts of the following: 2 x 10 = 20
- aElaborate analogue based drug design giving emphasis on obje ctives and categories of analogue designing
- bDiscuss Hammet’s substituent c onstant, Taft’s steric constant and Hansch analysis and its role in predicting biological activity
- cDefine pharmacophore. Discuss concept of pharmacophore mappi ng and pharmacophore-based screen
Section CAttempt any five parts of the following: 7 x 5 = 35
- aWhat is molecular docking? How does flexible docking differ from rigid docking in molecular docking studies?
- bHow does chemoinformatics contribute to drug discovery? Expl ain steps involved in chemical data curation
- cDiscuss various energy minimization techniques used in molec ular modelling study
- dHow do similarity-based methods in virtual screening help id entify potential drug candidates? Discuss key techniques used to measure molecular similarity
- eDefine and classify bio-isosters. Explain bio-isosterism app roach with examples
- fDiscuss the role of molecul ar mechanics in drug design
- gWrite an elaborative note on De novo drug design with exampl e
- aDefine log P and explain how it relates to the partition coefficient
- bHow does QSAR differ from SAR, and what advantages does it o ffer?
- cWhat is a biochemical database?
- dCompare random screening and non-random screening approaches
- eWhat is conformatio nal analysis, and why is it important in SAR of a drug molecule?
- fWhat is bioinformatics, and h ow is it used in modern biological research?
- gEnlist two ADM E databases
- hName any two physicochemical properties commonly used to ass ess drug-likeness i. Explain COMFA and COMSIA. j. What is lead optimiza tion in drug discovery?
Question text is extracted from the official AKTU question paper PDF above. Hindi translations are omitted — every question is printed in English in the original paper. Last verified: 2026-08-23.
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