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Secosteroid

From Wikipedia, the free encyclopedia
Class of chemicals derived from steroids

[1]

Cholecalciferol, an example of a 9,10-secosteroid.IUPAC-approved carbon numbering and ring labeling is shown in the picture. Since secosteroids are derived from steroids, they retain the same labeling system as steroids.[1]: §3S-8 
The parent steroid skeleton. The B-ring of the parent steroid is broken between C9 and C10 to yield D vitamins.

Asecosteroid (/ˈsɛkˌstɛrɔɪd/) is a type ofsteroid with a "broken" ring. The wordsecosteroidderives from the Latin verbsecare meaning "to cut",[2]: 241  and 'steroid'. Secosteroids are described as a subclass of steroids under theIUPAC nomenclature.[1]: §3S-1 [3] Some sources instead describe them as compounds derived from steroids.[4]

Types or subclasses of secosteroids are defined by the carbon atoms of the parent steroid skeleton where the ring cleavage has taken place. For example, 9,10-secosteroids are derived fromcleavage of the bond between carbon atoms C9 and C10 of the steroid B-ring (similarly 5,6-secosteroids, 13,14-secosteroids, etc.).[1]: §3S-8 

The prototypical secosteroid ischolecalciferol (vitamin D3).[5] Its IUPAC systematic is "(5Z,7E)-(3S)-9,10-secocholestra-5,7,10(19)-trien-3-ol".[1]: §3S-8 

Somenonsteroidal estrogens, likedoisynolic acid (cleaved on the D ring)[6] andallenolic acid,[citation needed] are also secosteroids or secosteroid-like compounds.

See also

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References

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  1. ^abcdeMoss GP and the Working Party of the IUPAC-IUB Joint Commission on Biochemical Nomenclature."The Nomenclature of Steroids". Queen Mary University of London. also available asMoss GP (1989)."Nomenclature of Steroids (Recommendations 1989)".Pure Appl. Chem.61 (10): 1786f.doi:10.1351/pac198961101783.
    1. abc Chapters3S-8 "Ring fission" and 3S-9 "Vitamin D group"
    2. ^ (esp. 3S-1.4, incl. note 4) "Steroids are compounds possessing the skeleton of cyclopenta[a]phenanthrene or a skeleton derived therefrom by one or more bond scissions or ring expansions or contractions."
  2. ^Ayers D (1972).Bioscientific Terminology. Tucson: University of Arizona Press.ISBN 978-0-8165-0305-6.
  3. ^Hill RA; Makin HL; Kirk DN; Murphy GM (1991).Dictionary of Steroids (1st ed.). London: Chapman & Hall.ISBN 978-0-412-27060-4.
  4. ^"Definition of secosteroid".Farlex Partner Medical Dictionary. TheFreeDictionary.com.A compound derived from a steroid in which there has been a ring cleavage.
  5. ^Hanson JR (2010). "Steroids: partial synthesis in medicinal chemistry".Nat Prod Rep.27 (6):887–99.doi:10.1039/c001262a.PMID 20424788.
  6. ^Meyers, CY; Kolb, VM; Gass, GH; Rao, BR; Roos, CF; Dandliker, WB (October 1988). "Doisynolic-type acids--uterotropically potent estrogens which compete poorly with estradiol for cytosolic estradiol receptors".Journal of Steroid Biochemistry.31 (4A):393–404.doi:10.1016/0022-4731(88)90307-x.PMID 3172773.

External links

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Steroid classification
C17
C18
C19
C20
C21
C23
C24
C27
Functional group
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