| Identification | Back Directory | [Name]
PHYTOSPHINGOSINE | [CAS]
13552-11-9 | [Synonyms]
3,4-Octadecanetriol, 2-amino-1
1,3,4-Octadecanetriol,2-amino-
(2S,3S,4S)-2-aminooctadecane-1,3,4-triol
Water-Soluble PHYTOSPHINGOSINE, Nano-Liposomal PHYTOSPHINGOSINE | [EINECS(EC#)]
202-538-3 | [Molecular Formula]
C18H39NO3 | [MOL File]
13552-11-9.mol | [Molecular Weight]
317.51 |
| Chemical Properties | Back Directory | [Melting point ]
136-138 °C(Solv: acetonitrile (75-05-8)) | [Boiling point ]
483.7±40.0 °C(Predicted) | [density ]
0.983±0.06 g/cm3(Predicted) | [pka]
11.91±0.45(Predicted) | [InChI]
InChI=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 | [InChIKey]
AERBNCYCJBRYDG-UHFFFAOYSA-N | [SMILES]
C(O)C(N)C(O)C(O)CCCCCCCCCCCCCC |
| Hazard Information | Back Directory | [Uses]
4-Hydroxysphiganine can be used as an oat lipid extraction for applying on skin care. It can also be used in pesticide formulation for delivery of active agent to the target, and can also be applied to assess neuronal toxicity. | [Definition]
ChEBI: 2-Amino-1,3,4-octadecanetriol is an amino alcohol. | [Biological Functions]
phytosphingosine (PHS) is a major LCB in some plants and is involved in cell signaling. Sphingolipidomic profiling revealed that PHS accumulates as early as 1 h after pathogen inoculation with virulent and avirulent strains of Pseudomonas syringae pv. tomato in Arabidopsis leaves.
| [References]
[1] So Yeon Seo. “Phytosphingosine induces systemic acquired resistance through activation of sphingosine kinase.” Plant Direct 5 10 (2021): e351. |
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