Alkaloids

Definition of Alkaloids

  • Alkaloids are nitrogen-containing natural compounds, primarily derived from amino acids, known for diverse pharmacological activities and often bitter taste.

Structural Features

  • Contain basic nitrogen atoms with complex ring and heterocyclic structures.
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Classification of Alkaloids

  • Based on biosynthetic origin or structure:
  • Pyridine/Piperidine: e.g., Nicotine
  • Indole: e.g., Vincristine
  • Quinoline/Quinolizidine: e.g., Quinine
  • Tropane: e.g., Cocaine, Atropine
  • Isoquinoline: e.g., Morphine, Reserpine
  • Purine: e.g., Caffeine

Biosynthesis

  • Derived from amino acids like ornithine, lysine, tyrosine, and tryptophan through complex enzymatic pathways.
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Occurrence in Nature

  • Primarily in plants (e.g., Solanaceae, Papaveraceae, Rubiaceae), also in some fungi and animals.

Biological Activities and Uses

  • Pharmaceuticals: Medications such as analgesics (morphine), stimulants (caffeine), and anti-malarials (quinine).
  • Toxicity: Serve as defense compounds.
  • Psychoactive Effects: Affect the central nervous system (e.g., cocaine, LSD).
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Examples of Alkaloids

  • Caffeine: Stimulant in coffee, tea, cacao.
  • Atropine: Tropane alkaloid for nerve agent/pesticide poisoning.
  • Quinine: Anti-malarial from cinchona bark.
  • Reserpine: Isoquinoline alkaloid used to treat high blood pressure and psychotic disorders.

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