9.1 Flashcards

(10 cards)

1
Q
  1. What is a drug?
A

A drug is a substance with a known chemical structure that produces a specific biological effect.

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2
Q
  1. How can a drug bind to its target?
A

A drug binds via complementary interactions—ionic, hydrogen, Van der Waals, and sometimes covalent bonds—based on matching charge, shape, and size.

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3
Q
  1. What does drug affinity mean?
A

Affinity is the strength with which a drug binds to its target; higher affinity means effective binding at lower concentrations.

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4
Q
  1. What is drug selectivity?
A

Selectivity is a drug’s ability to preferentially bind its intended target versus other similar molecules.

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5
Q
  1. Give examples of common drug targets.
A

Common targets include receptors (e.g., GPCRs, nuclear receptors), ion channels, enzymes, transporters, and nucleic acids.

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6
Q
  1. How can drugs modify target function?
A

Drugs may activate (agonist), inhibit (antagonist), enhance, attenuate, or interfere with a target’s function—such as by enzyme inhibition or acting as a prodrug.

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7
Q
  1. Why is complementarity important in drug binding?
A

Complementarity ensures that a drug’s charge, size, and shape match the binding site for specific and effective interactions.

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8
Q
  1. How do intermolecular forces contribute to drug-target interactions?
A

They provide the bonding forces (like ionic and hydrogen bonds) that secure the drug in its target’s binding site.

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9
Q
  1. Why is a high drug affinity desirable in therapy?
A

High affinity means the drug effectively binds at low doses, potentially reducing side effects and improving efficacy.

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10
Q
  1. How is drug selectivity achieved?
A

Selectivity is achieved when a drug has a significantly higher affinity for its intended target than for other molecules, minimizing off-target effects.

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