Code: | MI072216 | Acronym: | FTFGN1 |
Keywords | |
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Classification | Keyword |
OFICIAL | Physical Sciences |
Active? | Yes |
Web Page: | https://moodle.up.pt/course/view.php?id=78 |
Responsible unit: | Pharmacognosy Laboratory |
Course/CS Responsible: | MSc in Pharmaceutical Sciences |
Acronym | No. of Students | Study Plan | Curricular Years | Credits UCN | Credits ECTS | Contact hours | Total Time |
---|---|---|---|---|---|---|---|
MICF | 341 | Official Curriculum | 2 | - | 6 | 52 | 162 |
Knowledge of basic metabolic pathways of plant biosynthesis (particularly acetate and shikimate pathway,);
Knowledge of chemical groups and biosynthetic pathways of origin of secondary metabolites;
Knowledge of drugs of natural origin, either included or not in pharmacopoeias:
-with pharmacological actions and used in therapeutics
-containing starting materials for the semisynthesis of pharmacologically active molecules by the pharmaceutical industry
- containing auxiliary substances for pharmaceutical and food industries.
In a broad sense, the student will acquire knowledge on plant products with therapeutic activity and on active principles with pharmaceutical, cosmetic and food interest, or their toxicity, derived from plant species. The student will have an overview of the various uses of plant species and acquire knowledge on techniques applicable to their quality control.
1. Concepts of phytochemistry and pharmacognosy
2. Therapeutic use of drugs of plant origin
3. Microscopic analysis of plant drugs
4. Primary metabolites
4.1. Carbohydrates
4.1.1. Monosaccharides
4.1.2. Oligosaccharides
4.1.3. Polysaccharides
4.1.3.1. Bacteria and fungi polysaccharides
4.1.3.2. Algae polysaccharides
4.1.3.3. Vascular plants polysaccharides
4.1.3.3.1. Homogeneous polysaccharides
4.1.3.3.1.1. Starch
4.1.3.3.1.2. Cellulose
4.1.3.3.1.3. Frutans
4.1.3.3.2. Heterogeneous polysaccharides
4.1.3.3.2.1. Gums
4.1.3.3.2.2. Mucilages
4.1.3.3.2.3. Pectic substances
4.2. Lipids
5. Secondary metabolites
5.1. Acetyl-coenzyme A and acetate pathway metabolites
5.1.1. Quinones
5.1.1.1. Biosynthesis and classification
5.1.1.2. Physicochemical properties and analysis
5.1.1.3. Pharmacological activity and therapeutic use
5.1.1.4. Naphthoquinone-containing plant drugs
5.1.1.5. Anthraquinone-containing plant drugs
5.1.1.6. Naphthodiantrone-containing plant drugs
5.1.2. Orcinols and phloroglucinols
5.1.2.1. Biosynthesis
5.1.2.2. Pharmacological activity
5.1.2.3. Plant drugs with these compounds
5.2. Shikimic acid and shikimic acid pathway metabolites
5.2.1. Simple phenols and phenolic acids
5.2.1.1. Biosynthesis
5.2.1.2. Physicochemical properties and analysis
5.2.1.3. Simple phenol-containing plant drugs
5.2.1.4. Phenolic acid-containing plant drugs
5.2.2. Coumarins
5.2.2.1. Biosynthesis
5.2.2.2. Physicochemical properties and analysis
5.2.2.3. Pharmacological activity and therapeutic use
5.2.2.4. Plant drugs with these compounds
5.2.3. Lignans, neolignans and related compounds
5.2.3.1. Biosynthesis
5.2.3.2. Pharmacological activity and therapeutic use
5.2.3.3. Plant drugs with these compounds
5.2.4. Diarylheptanoids, arylalkanones and stilbenoids
5.2.4.1. Biosynthesis
5.2.4.2. Physicochemical properties and analysis
5.2.4.3. Pharmacological activity and therapeutic use
5.2.4.4. Plant drugs containing these compounds
5.2.5. Xanthones
5.2.5.1. Biosynthesis
5.2.5.2. Physicochemical properties and analysis
5.2.5.3. Pharmacological activity and therapeutic use
5.2.5.4. Xanthone-containing plant drugs
5.2.6. Flavonoids
5.2.6.1. Biosynthesis, chemical structure and classification
5.2.6.2. Physicochemical properties and analysis
5.2.6.3. Biological properties and therapeutic use
5.2.6.4. Flavonoid-containing drugs
5.2.7. Tannins
5.2.7.1. Biosynthesis, chemical structure and classification
5.2.7.2. Physicochemical properties and analysis
5.2.7.3. Biological properties and therapeutic use
5.2.7.4. Tannin-containing drugs
The course unit of Phytochemistry and Pharmacognosy I is included in the Moodle e-learning platform provided by the Office of Support for New Technologies in Education, UP. Thus, the presentations given in the lessons will be available in the platform. The platform also includes a forum to address the subjects from a different perspective of the lessons.
Theoretical lessons: 2 h/week. Presentations in "data show" (powerpoint software).
Laboratorial lessons: 2 h/week. In the beginning of the semester a laboratory handbook is supplied to the students, where they will find the protocols of the works to be performed and the respective theoretical explanation. Each laboratorial work will be carried out by groups of two students. Whenever possible, the laboratorial work will correspond to the content of the theoretical lectures, in order to facilitate their interconnection.
designation | Weight (%) |
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Exame | 100,00 |
Total: | 100,00 |
designation | Time (hours) |
---|---|
Frequência das aulas | 48,00 |
Total: | 48,00 |
The assistance of students to theoretical lectures is not mandatory.
The assistance of students to laboratory lectures is mandatory. Students with less than 75% attendance of effectively given lectures are considered not eligible for the exam.
In the final classification, the laboratory component corresponds to 25%, with the remaining 75% allocated to the written test.
Students with a grade of less than 50% (2.5 points) of the value of the laboratory component in the evaluation of the course unit are considered failed and must perform a practical final exam.
Students who obtain a score on the written test less than 46.67% (7.0 points) of the value of the written component in the evaluation of the course unit are considered failed.
There is neither specific evaluation nor special assignments, except for those cases prescribed by law for students included in special regimens.
According to the general law and the rules adopted by the Educational Council.
The improvement of classification consists of a practical test (optional) and a written test, covering all subjects taught in the lessons.
Prerequisites: knowledge of chemistry, including the distribution of chemical compounds by families and solubility characteristics of the compounds (acquired in the courses of General and Inorganic Chemistry, and Organic Chemistry I and II).
On March 7, 2020, the Faculty of Pharmacy of the University of Porto was closed, as a positive case of SARS-CoV-2 infection was identified. Additionally, the pandemic caused by this virus led to the establishment of a State of Emergency in Portugal, which was associated with a Contingency Plan.
Despite the changes imposed to the "Teaching Methods and Learning Activities", resulting from the application of the Covid-19 Contingency Plan, the UC program was taught in its entirety with the adjustments shown below:
The measurement of knowledge of the practical component took place at a distance (and not in person), through the Moodle test, in the last week of May, within the schedule that was assigned to each class. The evaluation was carried out using mechanisms to guarantee academic integrity. Students who did not achieve a classification corresponding to 50% (2.5 points) of the value of the laboratory component in the UC evaluation were considered to have failed, as provided for in the UC form, and will have to take a new test, which will also take place at a distance (and not in person), using the Moodle test, on the date specified in the exam schedule. The evaluation takes place using academic integrity guarantee mechanisms.
The evaluation of the theoretical component will take place at a distance (and not in person), using the Moodle test, on the date specified in the exam calendar. The evaluation takes place using academic integrity guarantee mechanisms.