Exam Details

Subject advanced medicinal chemistry
Paper
Exam / Course m.pharm
Department
Organization Gujarat Technological University
Position
Exam Date January, 2019
City, State gujarat, ahmedabad


Question Paper

Seat No.: Enrolment
GUJARAT TECHNOLOGICAL UNIVERSITY
M.PHARM SEMESTER EXAMINATION -WINTER 2018
Subject Code: MPC103T Date: 05/01/2019
Subject Name: Advanced Medicinal Chemistry
Time :10:30 AM TO 01:30 PM Total Marks: 80
Instructions:
1. Attempt any five questions.
2. Make Suitable assumptions wherever necessary.
3. Figures to the right indicate full marks.
Q.1

Enumerate stages of drug discovery and explain methods of lead discovery.
06

Explain the theories involved in drug receptor interaction.
05

Why we required lead optimization? Explain methods involved in lead optimization.
05
Q.2

Add a note on rational behind prodrug design.
06

Explain strategies to combat drug resistance in antibiotics therapy.
05

Why is cancer so difficult to cure? Explain with drug resistance.
05
Q.3

Why analog design important in drug design? Explain any one strategy involved in analog design.
06

Write recent advancement in anticancer agents.
05

Why stereochemistry is important in drug action?
05
Q.4

Explain the strategies involved in development antiviral agents.
06

Explain enzyme kinetics principles of enzyme inhibitors.
05

Add a note on enzyme inhibitors in basic research.
05
Q.5

Explain design of peptidomimetics.
06

Explain chemistry of prostaglandins, leukotrienes and thromboxanes.
05

Add a note on identification, validation and diversity of drug targets.
05
Q. 6

Explain latest development of antihypertensive medication.
06

Add a note on carrier linked prodrugs.
05

Explain simplification approach in lead optimization
05
Q.7

Explain non-covalently and covalently binding enzyme inhibitors.
06

Add a note on COX-1 COX-2 inhibitors.
05

Explain H1 H2 receptor antagonists.
05



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Subjects

  • advanced medicinal chemistry
  • advanced organic chemistry-i
  • advanced organic chemistry-ii
  • advanced pharmacology ii
  • advanced pharmacology-i
  • advances in drug delivery system
  • advances in pharmacology
  • applied pharmacotherapeutics - ii
  • applied pharmacotherapeutics-i
  • audits and regulatory compliance
  • biological evaluations & clinical research
  • cellular and molecular pharmacology
  • clinical and hospital pharmacy
  • clinical pharmacy practice
  • clinical research and pharmacy practice
  • clinical research and regulatory affairs
  • clinical research regulations
  • cosmetic and cosmeceuticals
  • documentation and regulatory writing
  • drug design and discovery
  • drug regulation and regulatory authority
  • experimental design and patents
  • global regulatory requirements
  • gmp, glp and validation
  • good manufacturing and good laboratory practice
  • good manufacturing practice and process validation
  • good regulatory practices
  • hazards and safety management
  • industrial pharmacy practice
  • modern analytical techniques
  • modern pharmaceutical analysis
  • novel drug delivery system part-i
  • novel drug delivery system-ii
  • pharm. management -ii
  • pharmaceutical analysis ii
  • pharmaceutical and cosmetic analysis
  • pharmaceutical formulation and development
  • pharmaceutical formulation development and biopharmceutics
  • pharmaceutical manufacturing technology
  • pharmaceutical production management & technology
  • pharmaceutical regulatory affairs
  • pharmacological and toxicological screening methods-i
  • pharmacological and toxicological screening methods-ii
  • pharmacometrics and methods of biological evaluation of drugs
  • pharmacotherapeutics
  • principles of biopharmaceutics& pharmacokinetics
  • product development and technology transfer
  • quality control & quality assurance
  • quality control and quality assurance
  • quality management system
  • regulatory affairs - i
  • regulatory affairs and new drug applications
  • regulatory aspects of hebbal and biologicals
  • research methodology
  • validation and product development