| 词条 | Phytosphingosine |
| 释义 |
| ImageFile = Phytosphingosine.svg | ImageSize = 200px | ImageAlt = Chemical structure of phytosphingosine | IUPACName = (2S,3S,4R)-2-Aminooctadecane-1,3,4-triol | OtherNames = {{bulletedlist|Hydroxysphinganine | D-ribo-Phytosphingosine | (4R)-Hydroxysphinganine}} | Section1 = {{Chembox Identifiers | CASNo = 554-62-1 | UNII=GIN46U9Q2Q | PubChem = 122121 | EC_number = 439-210-6 | ChEBI = 46961 | ChEMBL = 236036 | KEGG = C12144 | Beilstein = 1725301 | ChemSpiderID = 108921 | StdInChI=1S/C18H39NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17(21)18(22)16(19)15-20/h16-18,20-22H,2-15,19H2,1H3/t16-,17+,18-/m0/s1 | StdInChIKey = AERBNCYCJBRYDG-KSZLIROESA-N | SMILES = CCCCCCCCCCCCCC[C@H]([C@H]([C@H](CO)N)O)O | Section2 = {{Chembox Properties | C=18|H=39|N=1|O=3 | Appearance = | Density = | MeltingPtC = 102-103 | BoilingPt = | Solubility = | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = | GHSPictograms = {{GHS05}}{{GHS09}} | GHSSignalWord = Danger | HPhrases = {{H-phrases|318|400|410}} | PPhrases = {{P-phrases|273|280|305+351+338|310|391|501}} }}Phytosphingosine is a sphingoid base, a fundamental building block of more complex sphingolipids. It is abundant in plants and fungi and present in animals.[1] References1. ^{{Cite journal|last=Park|first=Moon-Taek|last2=Kang|first2=Jung A.|last3=Choi|first3=Jung-A.|last4=Kang|first4=Chang-Mo|last5=Kim|first5=Tae-Hwan|last6=Bae|first6=Sangwoo|last7=Kang|first7=Seongman|last8=Kim|first8=Sujong|last9=Choi|first9=Weon-Ik|date=February 2003|title=Phytosphingosine induces apoptotic cell death via caspase 8 activation and Bax translocation in human cancer cells|journal=Clinical Cancer Research|volume=9|issue=2|pages=878–885|issn=1078-0432|pmid=12576463}} {{organic-compound-stub}} 3 : Lipids|Amines|Triols |
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