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	<title>鞘氨醇 - 版本历史</title>
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		<title>123.130.221.191：建立内容为“{{Chembox | ImageFile = Sphingosine-2D-skeletal.png | ImageSize =  | ImageName = Sphingosine | IUPACName = (2''S'',3''R'')-2-aminooctadec-4-ene-1,3-diol | OtherNa…”的新页面</title>
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		<summary type="html">&lt;p&gt;建立内容为“{{Chembox | ImageFile = Sphingosine-2D-skeletal.png | ImageSize =  | ImageName = Sphingosine | IUPACName = (2&amp;#039;&amp;#039;S&amp;#039;&amp;#039;,3&amp;#039;&amp;#039;R&amp;#039;&amp;#039;)-2-aminooctadec-4-ene-1,3-diol | OtherNa…”的新页面&lt;/p&gt;
&lt;p&gt;&lt;b&gt;新页面&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{Chembox&lt;br /&gt;
| ImageFile = Sphingosine-2D-skeletal.png&lt;br /&gt;
| ImageSize = &lt;br /&gt;
| ImageName = Sphingosine&lt;br /&gt;
| IUPACName = (2''S'',3''R'')-2-aminooctadec-4-ene-1,3-diol&lt;br /&gt;
| OtherNames = &lt;br /&gt;
| Section1 = {{Chembox Identifiers&lt;br /&gt;
| CASNo = 123-78-4&lt;br /&gt;
| PubChem = 1104&lt;br /&gt;
| SMILES = N[C@@H](CO)[C@H](O)\C=C\CCCCCCCCCCCCC&lt;br /&gt;
}}&lt;br /&gt;
| Section2 = {{Chembox Properties&lt;br /&gt;
| C = 18 | H = 37 | N = 1 | O = 2&lt;br /&gt;
| Formula = &lt;br /&gt;
| MolarMass = &lt;br /&gt;
| Appearance = &lt;br /&gt;
| Density = &lt;br /&gt;
| MeltingPt = &lt;br /&gt;
| BoilingPt = &lt;br /&gt;
| Solubility = &lt;br /&gt;
}}&lt;br /&gt;
| Section3 = {{Chembox Hazards&lt;br /&gt;
| MainHazards = &lt;br /&gt;
| FlashPt = &lt;br /&gt;
| Autoignition = &lt;br /&gt;
}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
'''鞘氨醇'''（Sphingosine）又称'''[[神经]]鞘氨醇'''，[[学名]]2-氨基-4-十八烯-1,3-[[二醇]]，是一种含有不饱和烃基链的[[十八碳]]氨基醇。鞘氨醇属于[[鞘脂类]]，为[[细胞膜]]组成成分之一。&lt;br /&gt;
&lt;br /&gt;
==功能==&lt;br /&gt;
&lt;br /&gt;
鞘氨醇在体内可在两种[[激酶]]——[[鞘氨醇激酶]]1和鞘氨醇激酶2的[[催化]]下被[[磷酸化]]产生[[鞘氨醇-1-磷酸]]，后者是一种有力的信号脂[[类分子]]。&lt;br /&gt;
&lt;br /&gt;
[[鞘脂]]的[[代谢物]]如[[神经酰胺]]、鞘氨醇与鞘氨醇-1-磷酸，均为信号脂类分子，参与多种[[细胞]]过程。&lt;br /&gt;
&lt;br /&gt;
== [[生物合成]] ==&lt;br /&gt;
&lt;br /&gt;
[[棕榈酰]][[CoA]]与[[丝氨酸]]缩合，得到脱氢鞘氨醇。&lt;br /&gt;
&lt;br /&gt;
&amp;lt;br /&amp;gt; [[Image:Sphingosine synthesis corrected.png||800px|鞘氨醇合成]] &amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
然后脱氢鞘氨醇被NADPH还原为[[二氢鞘氨醇]]，后者再被FAD氧化为鞘氨醇。&lt;br /&gt;
&lt;br /&gt;
==参考资料==&lt;br /&gt;
* {{cite journal en|author=Radin N |title=Killing tumours by ceramide-induced apoptosis: a critique of available drugs |journal=Biochem J |volume=371 |issue=Pt 2 |pages=243–56 |year=2003 |pmid=12558497 |doi=10.1042/BJ20021878}} [http://www.biochemj.org/bj/371/0243/bj3710243.htm article]&lt;br /&gt;
* Carter, H. E., F. J. Glick, W. P. Norris, and G. E. Phillips. 1947. [http://www.jbc.org/cgi/reprint/170/1/285?ijkey=7fd093d3a30af91f599ef98c8f464caa5e41f203&amp;amp;amp;keytype2=tf_ipsecsha Biochemistry of the sphingolipides. III. Structure of sphingosine]. J. Biol. Chem. 170: 285–295&lt;br /&gt;
&lt;br /&gt;
==图片==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;gallery&amp;gt;&lt;br /&gt;
&lt;br /&gt;
 Image:Sphingolipidoses.svg|鞘[[脂贮积病]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/gallery&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==外部链接==&lt;br /&gt;
* {{MeshName|Sphingosine}}&lt;br /&gt;
&lt;br /&gt;
{{氨基醇}}&lt;br /&gt;
{{鞘脂}}&lt;br /&gt;
[[Category:生物分子]]&lt;br /&gt;
==参考来源==&lt;br /&gt;
*[http://zh.wikipedia.org/wiki/%E9%9E%98%E6%B0%A8%E9%86%87 维基百科-鞘氨醇]&lt;/div&gt;</summary>
		<author><name>123.130.221.191</name></author>
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