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Pharmaceutical Chemistry Flashcards

7 cards from real FPGEE practice questions. Tap to flip, then mark Knew It or Still Learning โ€” missed cards come back until you master them.

Read the first 7 Pharmaceutical Chemistry flashcards as text
  1. Which functional group is responsible for the acidic properties of aspirin?

    Answer: Carboxylic acid group

    The carboxylic acid (-COOH) group in aspirin (acetylsalicylic acid) donates a proton, conferring its acidic properties.

  2. The term 'prodrug' refers to a compound that:

    Answer: Requires metabolic conversion to exert its effect

    A prodrug is pharmacologically inactive until metabolized in the body to its active form.

  3. Which bond type is hydrolyzed during the metabolism of ester prodrugs?

    Answer: Ester bond

    Esterases in plasma and tissues cleave the ester bond, releasing the active drug from an ester prodrug.

  4. The Henderson-Hasselbalch equation is used primarily to predict:

    Answer: The degree of ionization of a drug at a given pH

    The Henderson-Hasselbalch equation relates pH, pKa, and the ratio of ionized to unionized drug forms.

  5. Which class of reaction is CYP3A4-mediated hydroxylation classified as?

    Answer: Phase I oxidation

    CYP3A4 is a cytochrome P450 enzyme that catalyzes Phase I oxidation reactions, including aromatic and aliphatic hydroxylation.

  6. Isomerism involving non-superimposable mirror images of a molecule is called:

    Answer: Enantiomerism

    Enantiomers are non-superimposable mirror images of each other, differing in the spatial arrangement around a chiral center.

  7. Which property of a drug is most directly improved by salt formation?

    Answer: Aqueous solubility

    Salt formation converts a poorly water-soluble drug into an ionized form that typically has significantly greater aqueous solubility.