SFAK20010U Medicinal and Biostructural Chemistry
MSc Programme in Pharmacy and Pharmaceutical Sciences (danish programmes cand.pharm and cand.scient.pharm) - compulsory
MSc Programme in Medicinal Chemistry - compulsory
MSc Programme in Pharmaceutical Sciences (english programme) - compulsory
The course deals with the most important principles of drug design and discovery of small molecules and biopharmaceuticals, including fundamental aspects of bioinformatics and structural biology. Genome structure will be introduced focusing primarily on the importance of systematic variations of the human genome in relation to diseases. Sequence alignment will be discussed and students will get to use internet based tools for sequence analyses. The course will cover examples of application of data science methods relevant in drug design. The course will give basic knowledge about the structure of proteins, including 3-D structural information and experimental methods for structure determination. Methods for design and development of substances - small molecules and biopharmaceuticals, in particular - with specific or selective effect on biochemical or physiological processes will be introduced. Emphasis will be on the significance of steric, stereo chemical, conformational and electrostatic factors for decision making in drug design. The importance of changes of structural and physico-chemical parameters in order to obtain drugs with appropriate pharmacokinetic properties will be discussed. The importance of the prodrug principle for improving the pharmacokinetic properties of drugs will also be addressed. Students will be introduced to systems biology and the importance of protein-protein interactions, and particular emphasis is on peptides and proteins as drugs, including peptidomimetics and peptide and protein design. Examples of structure-based design towards the main drug targets classes, e.g. receptors, transporters and enzymes, will be presented and covered in classes and practicals.
The course objective is to give students insight into the molecular mechanisms of action of selected drugs and to acquaint them with the fundamental principles of drug design and discovery. The course aims to expand students knowledge of the chemical and structural factors relating to the main drug groups and to give examples of the use of chemical principles to clarify the interaction of small molecule or biopharmaceutical drugs with macromolecules in the organism. This includes a basic understanding of the 3-D structure of drugs and target macromolecules. Students shall be able to use the vast amount of sequence and biostructural information on relevant target macromolecules available on internet databases, and to use such information about proteins primary sequences and 3-D structures of macromolecules in the context of drug design.
At the end of the course, students are expected to be able to:
Knowledge
- Define the concepts used to describe molecular interactions in the context of drug design and discovery
- Explain the principles of small molecules and biopharmaceutical drug actions on a number of biological targets
- Define the basic concepts from bioinformatics used in drug design and discovery
- Understand, reflect, explain and critically evaluate molecular interactions in the context of drug design and discovery
- Understand, reflect, explain and critically evaluate the principles of drug actions on a number of biological targets
- Understand, reflect and critically evaluate results from bioinformatics in drug design and discovery
Skills
- Master, discuss and evaluate the use of 3D-structures in ligand design
- Master, discuss and evaluate the use of the information available from sequenced genomes to solve problems related to drug design and discovery
- Master, discuss and evaluate the use of pharmacophores in drug design
- Master, discuss and evaluate the use of basic methodologies of receptor pharmacology in drug design
- Discuss and evaluate fundamental principles of peptide and protein design
- Assess, evaluate, independently discuss and present published research related to drug design and discovery.
Competences
- Independently plan and prepare presentations of published research
- Implement the use of the relationship between chemical structure and biological activity of important drug classes
- Take responsibility for and coordinate presentations of published research related to drug design and discovery
- Implement and develop further the use of 3D structures in ligand design
- Implement and develop further the use of the relationship between chemical structure and biological activity of important drug classes
- Textbook of Drug Design and Discovery, Povl Krogsgaard-Larsen, Kristian Strømgaard, Ulf Madsen (Eds.), 5th Edition, 2016, CRC Press
- Biochemistry. Jeremy M. Berg, John L. Tymoczo and Lubert Stryer, 7th edition, 2011
- Four scientific papers available at the course website
•10 class lessons as journal clubs (45-minutes)
•4 Four hour computer exercises
- Category
- Hours
- Lectures
- 31
- Class Instruction
- 9
- Preparation
- 102
- Theory exercises
- 16
- Guidance
- 48
- Total
- 206
Feedback is given to student presentations in class hours, which are in a 'journal club' format.
Open for credit transfer students and other external students. Apply here:
Credit transfer students:
Credit transfer student at SUND – University of Copenhagen
(ku.dk)
Other external students:
https://healthsciences.ku.dk/education/student-mobility/guest-students/
Credit transfer and other external students are welcomed on the course if there are seats available and they have the academic qualifications.
- Credit
- 2,5 ECTS
- Type of assessment
- Continuous assessment
- Type of assessment details
- In order to obtain the course certificate the student should participate actively during class lessons and computer practical exercises. Additionally, upload of completed quizzes are required.
- Marking scale
- passed/not passed
- Censorship form
- No external censorship
Criteria for exam assesment
To achieve a course certificate the student must be able to:
Knowledge
- Define the concepts used to describe molecular interactions in the context of drug design and discovery
- Explain the principles of drug actions on a number of biological targets
- Define the basic concepts from bioinformatics used in drug design and discovery
- Understand, reflect, explain and critically evaluate molecular interactions in the context of drug design and discovery
- Understand, reflect, explain and critically evaluate the principles of drug actions on a number of biological targets
- Understand, reflect and critically evaluate results from bioinformatics in drug design and discovery
Skills
- Master, discuss and evaluate the use of 3D-structures in ligand design
- Master, discuss and evaluate the use of the information available from sequenced genomes to solve problems related to drug design and discovery
- Master, discuss and evaluate the use of pharmacophores in drug design
- Master, discuss and evaluate the use of basic methodologies of receptor pharmacology in drug design
- Discuss and evaluate fundamental principles of peptide and protein design
- Assess, evaluate, independently discuss and present published research related to drug design and discovery.
Competences
- Independently plan and prepare presentations of published research
- Implement the use of the relationship between chemical structure and biological activity of important drug classes
- Take responsibility for and coordinate presentations of published research related to drug design and discovery
- Implement and develop further the use of 3D structures in ligand design
- Implement and develop further the use of the relationship between chemical structure and biological activity of important drug classes
- Credit
- 5 ECTS
- Type of assessment
- Written examination, 3 hours under invigilation
- Type of assessment details
- Individual 3-hour written examination.
Examination design:
The examination assignment typically consist of 3 assignments each with 5 sub-assignments. For each sub-assignment at least 3 possible answers are provided in a multiple choice format. Typically one of the 3 assignments deal with biostructural aspects, whereas the remaining two assignments are more medicinal chemistry focused. - Aid
- Written aids allowed
Find more information about written on-site exams in the exam rooms, incl. information about standard programs on the exam PCs at KUnet
In addition to the standard programs digital notes are permitted for this exam. It is allowed to upload notes for the ITX exam via digital exam. You will find a link to this feature from your exam in Digital Exam.
Students are also allowed to bring a molecular model building set.
- Marking scale
- 7-point grading scale
- Censorship form
- No external censorship
Criteria for exam assesment
To achieve the grade 12 the student must have:
Knowledge
- Define the concepts used to describe molecular interactions in the context of drug design and discovery
- Explain the principles of drug actions on a number of biological targets
- Define the basic concepts from bioinformatics used in drug design and discovery
- Understand, reflect, explain and critically evaluate molecular interactions in the context of drug design and discovery
- Understand, reflect, explain and critically evaluate the principles of drug actions on a number of biological targets
- Understand, reflect and critically evaluate results from bioinformatics in drug design and discovery
Skills
- Master, discuss and evaluate the use of 3D-structures in ligand design
- Master, discuss and evaluate the use of the information available from sequenced genomes to solve problems related to drug design and discovery
- Master, discuss and evaluate the use of pharmacophores in drug design
- Master, discuss and evaluate the use of basic methodologies of receptor pharmacology in drug design
- Discuss and evaluate fundamental principles of peptide and protein design
- Assess, evaluate, independently discuss and present published research related to drug design and discovery.
Competences
- Independently plan and prepare presentations of published research
- Implement the use of the relationship between chemical structure and biological activity of important drug classes
- Take responsibility for and coordinate presentations of published research related to drug design and discovery
- Implement and develop further the use of 3D structures in ligand design
- Implement and develop further the use of the relationship between chemical structure and biological activity of important drug classes
Course information
- Language
- English
- Course code
- SFAK20010U
- Credit
- See exam description
- Level
- Full Degree Master
- Duration
- 1 block
- Placement
- Block 2
- Schedule
- B
- Course capacity
- 265 students (reserved students at MSc Programme in Pharmacy or Pharmaceutical Sciences (danish programmes), students at MSc Programme in Pharmaceutical Sciences and students at MSc Programme in Medicinal Chemistry (english programmes).
Study board
- Study Board of Pharmaceutical Sciences
Contracting department
- Department of Drug Design and Pharmacology
Contracting faculty
- Faculty of Health and Medical Sciences
Course Coordinators
- Michael Gajhede (3-7d79775083857e743e7b853e747b)
Main responsible