Lipids: structure and classification: Difference between revisions

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== References ==
== References ==
*Molecular models in this page were created  or modificated from ''pdb'' files by [[User:Alejandro Porto|Alejandro Porto]] using the tool JSME Molecular Editor [http://biomodel.uah.es/en/DIY/JSME/draw.es.htm]
*Molecular models in this page were created  or modified from ''pdb'' files by [[User:Alejandro Porto|Alejandro Porto]] using the tool JSME Molecular Editor [http://biomodel.uah.es/en/DIY/JSME/draw.es.htm]
<references/>
<references/>

Revision as of 22:45, 5 February 2016

Lipids.
  • Fatty acids.-
    • , a saturated 16 carbon fatty acid. Look its , an its .
    • , a monounsaturated 18 carbon fatty acid. Most monounsaturated natural fatty acids are .
    • , a polyunsaturated 18 carbon fatty acid. con with cis configuration.
    • , another polyunsaturated 18 carbon fatty acid with
  • Saponifiables lipids.-
    • .- Zoom on .
    • Waxes.- for instance .
    • .- lipids composed of , , and a polar compound like .
    • Sphingolipids.- all o them include in their structure the amino alcohol . Sphingosine bind to a fatty acid to yield , the common structural feature of all sphingolipids.
  • Unsaponifiable lipids.-
    • Terpenes.- they are polymers of the 5 carbon unsaturated hydrocarbon named (2-methyl-1,3 butadiene). Some terpenes are , , , , and .
    • Steroids.- Some steroids are , and . is also a steroid.
    • Eicosanoids.- They are derived from unsaturated 20 carbon fatty acid named . are a class of eicosanoids.


Drag the structure with the mouse to rotate

ReferencesReferences

  • Molecular models in this page were created or modified from pdb files by Alejandro Porto using the tool JSME Molecular Editor [1]

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

Alejandro Porto, Eric Martz, Joel L. Sussman, Karsten Theis