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KIVO Med

Simple lipids: structure and properties

Glycerides, cerides and sterides: structures, nomenclature, storage, reactions and biological roles.

  • 25 explained questions
  • 21 flashcards
  • 136 estimated course minutes

Updated

What you will learn

  • Distinguish mono-, di- and triacylglycerols and apply sn nomenclature.
  • Relate glyceride properties and reactions to their storage role.
  • Describe ceride structure and protective roles.
  • Relate cholesterol and sterides to membranes, hormones, vitamin D, bile acids and pathological deposits.

Course outline

  1. Esters built around three alcohols

    Simple lipids share an ester bond, but the nature of their alcohol directs them towards storage, protection or cholesterol transport.

    10 min

  2. Glycerides: building and naming the molecule

    The number, identity and position of fatty acids attached to glycerol define each glyceride.

    22 min

  3. Triglycerides: diet and storage

    Highly hydrophobic and energy-rich, triglycerides concentrate fatty acids in droplets containing almost no water.

    18 min

  4. Glycerides: properties, hydrolysis and saponification

    The ester structure explains glyceride hydrophobicity, digestion by lipases and conversion into soaps.

    30 min

  5. Cerides: waxes with two long chains

    Joining a fatty acid to a long aliphatic alcohol produces a solid, hydrophobic and protective lipid.

    18 min

  6. Sterides: esterifying and transporting cholesterol

    Cholesterol’s –OH group enables either membrane insertion or esterification into an entirely non-polar form.

    24 min

  7. Connecting alcohol, property and function

    The nature of the alcohol directs a simple lipid towards storage, protection or cholesterol management.

    14 min

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