Science Quiz / Pharmacology Fun

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Can you name the Pharmacology Fun ?

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Type of receptor for endogenous ligand, neurotransmitter, hormones and MOST DRUGS
Type of receptor for antiinflammatory agents
Type of weak bond for highly lipid soluble drugs
A drug that binds to a different receptor, producing an effect that is OPPOSITE to that produced by the drug that it is antagonizing
Type of antagonist that shifts the agonist dose-response curve to the right
Type of binding site that binds to drugs without producing a direct biologic response
Route of administration of protein base and antibody drugs
What equation is this? Log(Protonated)/(Unprotonated) = pKa-pH
What is responsible for metabolism before the drug reaches the systemic circulation
Type of drug that is lipid soluble at acid pH and excreted faster in alkaline urine
Type of receptor for antibiotics, antineoplastic agents, and ASPIRIN
What equation is this? Flux= (C1-C2) Area*Permeability Coefficient/Thickness
Type of receptor for hormones, antibiotics, and antineoplastic agents
Type of antagonist where the ligand is covalently linked to the receptor
A drug that typifies the most important pharmacodynamic and many pharmacokinetic characteristics of that group
How many half lives are needed to reach steady state?
Initial dose to raise the concentration to steady state without waiting 4 half lives
Measure of the mobility of the drug molecules in the medium of the diffusion path
Produces an intracellular response
Type of receptor for alcohol and anesthetics
Dictates the time to steady state
Type of bond that is usually irreversible
Type of receptor for cardiac, CNS acting, and diuretic medications
Measure of the apparent space (volume) in the body available to contain the drug
Type of drug that is lipid soluble at alkaline pH and excreted faster in acidic urine
Type of kinetics for most drugs where a constant fraction of drug is eliminated per unit time
Type of graph that describes the relationship between drug concentration and response
Measure of the ability of the body to eliminate the drug
Type of kinetics where a constant amount of drug is eliminated per unit time
Type of graph that represents large numbers of individual patients' response to various drug concentrations
Fraction of unchanged drug reaching the SYSTEMIC CIRCULATION following administration by any route
Increases the sensitivity to the drug
More common type of bond that is short acting and has selectivity
Determines how much drug is necessary
Produces a lower response at full receptor occupancy than do full agonists

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Created Oct 2, 2010ReportNominate

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