About the content
This medicinal chemistry course explores how chemists modify a molecule’s structure to design a safe and effective drug.
This course opens with a brief history of drug discovery and introduces the modern drug approval process.Then, we will transition to learning about receptors and enzymes, the body’s molecules most often targeted by drugs.We will also discuss the topics of pharmacokinetics (drug adsorption, elimination, and half-life) and metabolism. The course closes with units on how potential drug molecules are identified and subsequently optimized into safe and effective drugs.
- How to measure the activity of enzymes and receptors
- Methods for modeling a drug’s half-life
- How to predict and alter the metabolism of a molecule
- Techniques for discovering molecules with desired biological activity
- Approaches for optimizing a molecule into a safe and effective drug
This course is offered through a collaboration between DavidsonX and the Novartis Institutes of BioMedical Research.
Courses offered via edX.org are not eligible for academic credit from Davidson College. A passing score in a DavidsonX course(s) will only be eligible for a verified certificate generated by edX.org.
High school level chemistry and biology and some experience with organic chemistry.
Basic math skills (logarithms and exponential functions) are also recommended.
Week 2: Drug Targets Structure of proteins Enzymes, enzymatic activity, and inhibition Receptors and molecules that modulate their activity Examination 1
Week 3: Pharmacokinetics Drug transport in the blood Clearance Volume of distribution Compartment modeling
Week 4: Metabolism Types of metabolic reactions Genetic and population effects Prodrugs Examination 2
Week 5: Binding, Structure, and Diversity Intermolecular forces Drug-target complementarity Molecular diversity and chemical libraries Combinatorial chemistry
Week 6: Lead Discovery Drug screening Filtering hits to find leads Existing drugs and natural products as leads
Week 7: Lead Optimization Functional group replacements Alkyl group replacements Isosteres and bioisosteres Peptidomimetics Examination 3
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