Akademik Dersler - İçerik

Will be able to list the properties of structure-activity relationships in pharmaceutical chemistry.
Will be able to define physicochemical properties in structure-activity relationships.
Describes structural features in structure-activity relationships.
Will be able to interpret the structure-activity relationships in drug molecules in terms of physicochemical properties.
Compares the structure-activity relationship in drugs in terms of solubility, partition coefficient and surface activity.
Distinguish the structure-activity relationship in drugs in terms of acid-base properties, ionization, stereochemistry, electronic properties.
Will be able to interpret the structure-activity relationships in drug molecules in terms of their structural properties.
Compares drug molecule and biological activity relationship in terms of steric properties, molecular connectivity index, isosterism, bioisosterism.
Distinguish between drug molecule and biological activity in terms of pharmacophore groups, metabolic stability and drug-receptor relationships.
Will be able to define quantitative structure-activity relationships (QSAR) in drug molecules.
Defines Hansch analysis, Free-Wilson analysis and Fujita-Ban analysis.
Reports computer-based methods.
Will be able to design new drug molecules according to structure-activity relationships.
Will be able to compare the functional groups on the drug molecule qualitatively and quantitatively.
Biologically interprets the structure-activity relationships of the functional groups on the drug molecule.