SAR of Local anaesthesia

SAR of Local Anaesthesia shows how lipophilic group, intermediate chain, and amine group influence potency, duration, and activity.

  1. Aromatic Group (Lipophilic End):

    • Typically, a benzene ring, responsible for lipophilicity, enabling penetration of nerve cell membranes.
    • Potency is proportional to lipid solubility, influencing membrane penetration.
  2. Intermediate Chain (Linker):

    • Connects the aromatic group to the ionizable group and determines metabolism and duration of action.
    • Ester-linked Anesthetics:
      • Metabolized by plasma cholinesterases.
      • Higher risk of allergic reactions.
    • Amide-linked Anesthetics:
      • Metabolized in the liver.
      • Lower allergy risk and longer duration of action.
  3. Ionizable Group (Hydrophilic End):

    • Usually a tertiary amine, contributing to hydrophilicity.
    • Degree of ionization affects onset of action:
      • Non-ionized form penetrates membranes.
      • Ionized form blocks sodium channels inside nerves, causing anesthesia.

Additional SAR Factors:

  • Stereochemistry: Enantiomers may differ in activity and toxicity (e.g., bupivacaine).
  • Intermediate Chain Length: Longer chains generally increase duration of action.
  • Aromatic Ring Substituents: Lipophilic groups enhance potency, while hydrophilic groups may reduce it.

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