03427 - Medicinal Chemistry II

Academic Year 2026/2027

  • Teaching Mode: In-person learning (entirely or partially)
  • Campus: Bologna
  • Corso: Single cycle degree programme (LMCU) in Pharmaceutical Chemistry and Technology (cod. 5986)

Learning outcomes

The course deals with the fundamental strategies of design and synthesis of drugs and with the molecular mechanism of drug action. the chemical structuresof drugs interacting with enzymes and receptorsand their structure-activity relationship.Particularly the student will be learn the principal classes of agents acting on central and peripheral nervous systems.

Course contents

Neurotransmitter receptors

The bonding of ligands to receptors. Structure and classification of receptors. General mode of operation. Ligand-response relationships: agonist and antagonist concentration-response relationships, partial agonism, inverse agonism. Ligand-receptor theories: Clark's occupancy theory, the rate theory, two-state model, perturbation theory. Classification, localization, function, structure, active site of adrenergic receptors, cholinergic receptors, dopaminergic receptors, GABAergic receptors, and opioid receptors.

Neurotransmitters

Acetylcholine, catecholamines, serotonin, histamine, 4-aminobutyric acid, enkephalins: biosynthesis, release, uptake, metabolism, molecular properties, active conformation, stereochemical properties.

Drugs acting at neurotransmitter receptors and enzymes

Structure-activity relationships, mechanism and site of action, therapeutic use, side effects, stereochemistry, and synthetic aspects of drugs acting at adrenergic, dopaminergic, cholinergic, serotoninergic, histaminergic, GABAergic, and opioid systems. Acetylcholine esterase inhibitors. Angiotensin–Converting Enzyme Inhibitors. Stereochemistry and synthesis of selected drugs:succinylcholine, atracurium, pancuronium, atropine, trihexyphenidyl, tropicamide, dicycloverine, donepezil, physostigmine, adrenaline, ethylephrine, ephedrine, clonidine, prazosin, salbutamol, reproterol, general synthesis of aryloxypropanolamines, practolol, diphenhydramine, promethazine, ranitidine, disodium cromoglycate, omeprazole, chlorpromazine, fluphenazine, clozapine, chlordiazepoxide, triazolam, oxazepam, diazepam, fentanyl, etorfine and fluoxetine.

Drug design

Basic principles of rational drug design. Drug design strategies. Modification of a lead compound.

Readings/Bibliography

For further readings, please refer to:

A. GASCO, F. GUALTIERI, C. MELCHIORRE, Chimica Farmaceutica, CEA, Milano, 2019

G. COSTANTINO, G: SBARDELLA, Chimica Farmaceutica, EdiSES, Napoli, 2024, I edizione.

D.A. WILLIAMS, T.L. LEMKE, Foye's Principi di Chimica Farmaceutica, VI Edizione italiana, Piccin, Padova, 2014.

Teaching methods

The course includes theoretical lessons and attendance is mandatory. The theoretical lessons are designed to convey to the student the knowledge of the main synthetic strategies for drug preparation, the mechanisms of action of agonists and antagonists that act on the different receptor systems and the structure-activity relationships of drugs.

Assessment methods

The assessment consists of both a written and an oral examination.

As a preliminary test, the student should describe the synthesis of two drugs among those in the program. If this test is passed, the examination continues with a discussion on two topics of the course . The student can also choose to take the oral interview in the immediately following session, as long as it is within the same exam session. Two appeals will be guaranteed in February, one appeal in June, one in July and two appeals in September. In the event that, after having passed the test relating to the synthesis, the oral test is not passed in the following session or the student does not appear for the session, the exam must be re-sit entirely. The registration on AlmaEsami is required.

The use of AI is forbidden. Any use of it is a violation of academic integrity.

Students with Specific Learning Disorders (SLD) or temporary or permanent disabilities: Students are encouraged to contact the University's dedicated support office well in advance (https://site.unibo.it/studenti-con-disabilita-e-dsa/it ). The office will propose any appropriate accommodations for eligible students. Any such accommodations must be submitted to the course instructor for approval at least 15 days in advance. The instructor will assess their suitability, taking into account the intended learning outcomes of the course.

Teaching tools

The teaching material (slides) presented during classes is available on the Virtuale platform.

Links to further information

https://www.unibo.it/sitoweb/michela.rosini/

Office hours

See the website of Michela Rosini

SDGs

Good health and well-being Industry, innovation and infrastructure Responsible consumption and production

This teaching activity contributes to the achievement of the Sustainable Development Goals of the UN 2030 Agenda.