M PHARM /CHEMISTRY OF NATURAL PRODUCTS – THEORY
After a successful completion of the course the students will be able to
| Course outcome number |
Course Outcomes |
Cognitive level |
| CO1 | Recall the fundamental structures and classifications of alkaloids. | C1 |
| CO2 | Explain the diverse roles of alkaloids in pharmaceutical applications. Interpret the pharmacological relevance of flavonoid structures. Explain the biological actions of steroids based on their structures. Comprehend the biosynthesis pathways of terpenoids. Explain the molecular mechanisms underlying vitamin functions. Comprehend the role of recombinant DNA technology in identifying potential drug targets. | C2 |
| CO3 | Apply knowledge of alkaloid structures to predict their pharmacological properties. Apply understanding to correlate flavonoid structures with their medicinal properties. Apply knowledge to predict the potential activities of modified steroid structures. Apply knowledge to assess the therapeutic potential of specific terpenoid classes. Apply knowledge to elucidate the consequences of vitamin deficiencies. Apply knowledge to design strategies using recombinant DNA for drug discovery. | C3 |
| CO4 | Analyze the impact of different structural modifications on flavonoid activity. Analyze the impact of structural diversity on terpenoid bioactivity. | C4 |
| CO5 | Evaluate the relationship between steroid structures and their diverse biological effects. Evaluate the significance of vitamins in maintaining physiological balance. | C5 |
| CO6 | Develop novel approaches integrating recombinant DNA techniques for pharmaceutical innovation. | C6 |
Remembering (C1), Understanding (C2), Applying (C3), Analyzing (C4), Evaluating (C5) and Creating (C6)
