Steroid

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Steroid skeleton of lanosterol. The total number of carbons (30) reflects its triterpenoid origin. In some steroids some carbons may be removed (such as carbon 18) or added (such as carbons 241 and 242) in downstream biosynthetic reactions.
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Steroid skeleton of lanosterol. The total number of carbons (30) reflects its triterpenoid origin. In some steroids some carbons may be removed (such as carbon 18) or added (such as carbons 241 and 242) in downstream biosynthetic reactions.

A steroid is a terpenoid lipid characterized by a carbon skeleton with four fused rings. Different steroids vary in the functional groups attached to these rings. Hundreds of distinct steroids have been identified in plants, animals, and fungi. All steroids are derived either from the sterol lanosterol (animals and fungi) or the sterol cycloartenol (plants). Both sterols are derived from the cyclization of the triterpene squalene[1].

Contents

[edit] Classification

[edit] Taxonomical/Functional

Some of the common categories of steroids include:

[edit] Structural

It is also possible to classify steroids based upon their chemical composition. One example of how MeSH performs this classification is available at Wikipedia:MeSH_D04#MeSH_D04.808_---_steroids.

some classifications are michaels nelson and his huge pecs and how he can bench the world he basically has no genitles

[edit] Origin

Sex steroids include estrogen (U.S spelling) or oestrogen (UK spelling), progesterone and androgen. Oestrogen and progesterone are made primarily in the ovary and in the placenta during pregnancy and testosterone in the testis.

[edit] External links

[edit] References

  1. ^ http://www.chem.qmul.ac.uk/iubmb/enzyme/reaction/terp/lanost.html