Zymosterol: Difference between revisions

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fix double param in Chembox, per CAT:DUPARG. (Use temp convert; m: check symbol formatting; simple ws usage; rm setting dflt imagesize; rm dbl InChI) using AWB
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| ImageFile = zymosterol.png
| ImageSize =
| ImageFile1 = Zymosterol molecule ball.png
| IUPACName = (3''S'',5''S'',10''S'',13''R'',14''R'',17''R'')-10,13-dimethyl-17-[(2''R'')-6-methylhept-5-en-2-yl]-2,3,4,5,6,7,11,12,14,15,16,17-dodecahydro-1''H''-cyclopenta[''a'']phenanthren-3-ol
| ImageSize1 = 250
| OtherNames = 5α-Cholesta-8,24-dien-3β-ol
| ImageAlt1 = Ball-and-stick model of zymosterol
| OtherNamesIUPACName = 5α-Cholesta-8,24-dien-3β-ol
| IUPACNameSystematicName = (31''SR'',53a''SR'',105a''S'',137''RS'',149a''RS'',1711a''R'')-109a,1311a-dimethylDimethyl-171-[(2''R'')-6-methylhept-5-en-2-yl]-2,3,3a,4,5,5a,6,7,118,129,149a,1510,1611,1711a-dodecahydrotetradecahydro-1''H''-cyclopenta[''a'']phenanthren-37-ol
| OtherNames =
|Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 128-33-6
| CASNo_RefUNII_Ref = {{cascitefdacite|correct|??FDA}}
| UNII = PU2755PT4O
| PubChem = 92746
| CASNo_Ref = {{cascite|correct|??}}
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 83724
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| StdInChIKey = CGSJXLIKVBJVRY-XTGBIJOFSA-N }}
|Section2={{Chembox Properties
| C = 27 | H = 4 | O = 1
| Formula = C<sub>27</sub>H<sub>44</sub>O
| MolarMass = 384.64 g/mol
| Appearance =
| Density =
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}}
 
'''Zymosterol''' is aan intermediate in [[cholesterol]] intermediatebiosynthesis.<ref>{{Cite injournal | doi = 10.1021/ja00183a042 | title = Synthesis of zymosterol, fecosterol, and related biosynthetic sterol intermediates | date = 1989 | last1 = Dolle | first1 = Roland E. | last2 = Schmidt | first2 = Stanley J. | last3 = Erhard | first3 = Karl F. | last4 = Kruse | first4 = Lawrence I. | journal = Journal of the cholesterolAmerican biosynthesisChemical Society | volume = 111 | issue = 1 | pages = 278–284 | bibcode = 1989JAChS.111..278D }}</ref> Disregarding some intermediate compounds (e.g. 4-4-dimethylzymosterol), [[lanosterol]] can be considered a precursor of zymosterol in the cholesterol synthesis pathway. The conversion of zymosterol into cholesterol happens in the [[endoplasmic reticulum]]. Zymosterol accumulates quickly in the plasma membrane coming from the [[cytosol]]. The movement of zymosterol across the cytosol is more than twice as fast as the movement of cholesterol itself.
 
==References==
 
{{steroid-stubreflist}}
 
{{Cholesterol and steroid intermediates}}
 
{{steroid-stub}}
 
[[Category:Cholestanes]]
[[Category:Sterols]]