| Term 
 
        | Define structurally non-specific drugs |  | Definition 
 
        | Drugs which do not require specific sites of action 
 Biologic effect is related to physical properties (instead of chemical structure)
 |  | 
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        | Term 
 
        | Give an example of a structurally non-specific drug |  | Definition 
 
        | Osmotic diuretics, gastric antacids, general anesthetics, antiseptics (iodine, peroxide, alcohols, etc) |  | 
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        | Term 
 
        | Define structurally specific drugs |  | Definition 
 
        | Agents that usually interact with a specific protein to initiate a specific biological response or transduction of a signal |  | 
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        | Term 
 
        | List the four levels of protein structure |  | Definition 
 
        | 1': AA sequence 2': α-helix or β-sheet
 3': 3D shape, with binding pocket
 4": polypeptide assembly
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        | Term 
 
        | List four protein targets of drugs |  | Definition 
 
        | 1. Receptors 2. ion channels
 3. Enzymes
 4. transporters
 |  | 
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        | Term 
 
        | What two interactions allow a complementary fit between a ligand and active site? |  | Definition 
 
        | 1. Steric (shape) 2. Physiochemical (attractions by functional groups)
 |  | 
        |  | 
        
        | Term 
 
        | List the three Van der Waals interactions |  | Definition 
 
        | 1. Dipole-dipole (including H bonds) 2. Dipole-induced dipole
 3. Induced-dipole-induced dipole (LDF)
 |  | 
        |  | 
        
        | Term 
 
        | Define cation-pi interaction |  | Definition 
 
        | A non-covalent molecular interaction between the face of an electron rich π system (ex. benzene) and an adjacent cation |  | 
        |  | 
        
        | Term 
 
        | Define hydrophobic effect |  | Definition 
 
        | When two aklyl chains approach one another, water is extruded from the space between them, resulting in decreased energy and increased entropy |  | 
        |  | 
        
        | Term 
 
        | What are the two types of steric complementarity? |  | Definition 
 
        | 1. Entiomerism 2. Geometric isomerism
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | An active or desired entiomer |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | An entiomer without activity or with undesired activity |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | The portion of a drug that is responsible for its biological action |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | A biologically active compound as a starting point for chemical modification in order to improve potency, selectivity, or pharmacokinetic parameters |  | 
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        | Term 
 
        | List some ways scientists discover a lead compound |  | Definition 
 
        | -Random screening -Nonrandom screening
 -Drug metabolism studies
 -Clinical observation
 -Rational approaches
 |  | 
        |  | 
        
        | Term 
 
        | List some ways scientists modify a lead compound |  | Definition 
 
        | -Identify the pharmacophore -Modify functional groups
 -Structure-activity relationship (SAR) study
 -Structure modification
 -Quantitative SAR
 -Molecular graphics-based design
 |  | 
        |  | 
        
        | Term 
 
        | Define chemical isoterism |  | Definition 
 
        | The similarity in physiochemical properties of ions, compounds, or elements due to the similar electronic structure (on periodic table) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Compounds with functional groups of similar spatial and electronic character, resulting in similar physiochemical properties or biological actions 
 A common way to generate marketable analogues of a known drug
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Structure-Activity Relationship 
 The relationship of the molecular structure of a compound with a biological property
 
 QSAR=quantitative SAR
 |  | 
        |  | 
        
        | Term 
 
        | What can functional group pKa on a drug influence? |  | Definition 
 
        | Ionization 
 Rates of dissolution/absorption
 |  | 
        |  | 
        
        | Term 
 
        | What can functional group logP on a drug influence? |  | Definition 
 
        | Solubility/permeability Rate of dissolution/absorption |  | 
        |  | 
        
        | Term 
 
        | What is Lipinski's Rule of 5? |  | Definition 
 
        | An active drug has no more than one violation of the following: 
 -No more than 5 H-bond donors
 -No more than 10 H-bond acceptors
 -A molecular mass not greater than 500 daltons
 -An octanol-water partition coefficient log P not greater than 5
 |  | 
        |  | 
        
        | Term 
 
        | How are structural types classified into groups? |  | Definition 
 
        | 1. Aromatic vs Non-aromatic 2. Mono-cyclic vs Multi-cyclic
 3. Homo-cyclic vs Hetero-cyclic
 |  | 
        |  | 
        
        | Term 
 
        | Define privileged scaffolds |  | Definition 
 
        | Molecular frameworks that are seemingly capable of serving as ligands for a diverse array of receptors |  | 
        |  | 
        
        | Term 
 
        | Describe the first phase of drug metabolism |  | Definition 
 
        | Oxidation, reduction, and hydrolysis |  | 
        |  | 
        
        | Term 
 
        | Describe the second phase of drug metabolism |  | Definition 
 
        | Conjugation reactions: acetylation, sulfation, glucuronidation |  | 
        |  | 
        
        | Term 
 
        | List some oxgenase enzymes involved in phase 1 of metabolism |  | Definition 
 
        | Cytochrome P450, flavin monooxygenase, alcohol DH, aldehyde DH |  | 
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