When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Sterol - Wikipedia

    en.wikipedia.org/wiki/Sterol

    Sterols are a subgroup of steroids with a hydroxyl group at the 3-position of the A-ring. [10] They are amphipathic lipids synthesized from acetyl-coenzyme A via the HMG-CoA reductase pathway. The overall molecule is quite flat. The hydroxyl group on the A ring is polar. The rest of the aliphatic chain is non-polar.

  3. Steroid - Wikipedia

    en.wikipedia.org/wiki/Steroid

    Major secosteroid subclasses are defined by the steroid carbon atoms where this scission has taken place. For instance, the prototypical secosteroid cholecalciferol, vitamin D 3 (shown), is in the 9,10-secosteroid subclass and derives from the cleavage of carbon atoms C-9 and C-10 of the steroid B-ring; 5,6-secosteroids and 13,14-steroids are ...

  4. Polycyclic compound - Wikipedia

    en.wikipedia.org/wiki/Polycyclic_compound

    These ring substructures include cycloalkanes, aromatics, and other ring types. They come in sizes of three atoms and upward, and in combinations of linkages that include tethering (such as in biaryls), fusing (edge-to-edge, such as in anthracene and steroids), links via a single atom (such as in spiro compounds), bridged compounds, and ...

  5. Secosteroid - Wikipedia

    en.wikipedia.org/wiki/Secosteroid

    A secosteroid (/ ˈ s ɛ k oʊ ˌ s t ɛ r ɔɪ d /) is a type of steroid with a "broken" ring. The word secosteroid derives from the Latin verb secare meaning "to cut", [2]: 241 and 'steroid'. Secosteroids are described as a subclass of steroids under the IUPAC nomenclature. [1]: §3S-1 [3] Some sources instead describe them as compounds ...

  6. Gonane - Wikipedia

    en.wikipedia.org/wiki/Gonane

    Gonane is a tetracyclic hydrocarbon with no double bonds. It is formally the parent compound of the steroids, hence it is called the "steroid nucleus". [1] [4] [5] Some important gonane derivatives are the steroid hormones, characterized by methyl groups at the C10 and C13 positions and a side chain at the C17 position.

  7. Triterpene - Wikipedia

    en.wikipedia.org/wiki/Triterpene

    Steroids feature a cucurbitane core, although in practice they are biosynthesised from either lanosterol (animals and fungi) or cycloartenol (plants) via the cyclization of squalene. Steroids have two principal biological functions, being either key components of cell membranes or signaling molecules that activate steroid hormone receptors.

  8. List of androgens/anabolic steroids (alternate) - Wikipedia

    en.wikipedia.org/.../anabolic_steroids_(alternate)

    Steroid ring system. This is a list of androgens/anabolic steroids (AAS) or testosterone derivatives. Esters are mostly not included in this list; for esters, see here instead. The major classes of testosterone derivatives include the following (as well as combinations thereof):

  9. Spirolactone - Wikipedia

    en.wikipedia.org/wiki/Spirolactone

    Spirolactones are a class of functional group in organic chemistry featuring a cyclic ester attached spiro to another ring system. The name is also used to refer to a class of synthetic steroids, called steroid-17α-spirolactones, 17α-spirolactosteroids, or simply 17α-spirolactones, which feature their spirolactone group at the C17α position.