PS(18:0/18:0) (BioCAD00000025298)

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Metabolite Card

Formula: C42H82NO10P (791.5676)
SMILES: [H][C@](N)(COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC)C(O)=O

Synonyms [en]

PS(18:0/18:0); Distearoyl phosphatidylserine; 1,2-dioctadecanoyl-sn-glycero-3-phosphoserine; PS(36:0); Phosphatidylserine(36:0); PSer(36:0)

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

PS(18:0/18:0). 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China. https://biocad_registry.innovation.ac.cn/s/(-)-arctiin (retrieved 2026-01-03) (CAD Registry RN: BioCAD00000025298). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

PS(18:0/18:0) is a phosphatidylserine (PS or GPSer). It is a glycerophospholipid in which a phosphorylserine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, glycerophosphoserines can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PS(18:0/18:0), in particular, consists of one chain of stearic acid at the C-1 position and one chain of stearic acid at the C-2 position. The stearic acid moiety is derived from animal fats, coco butter and sesame oil, while the stearic acid moiety is derived from animal fats, coco butter and sesame oil. Phosphatidylserine or 1,2-diacyl-sn-glycero-3-phospho-L-serine is distributed widely among animals, plants and microorganisms. It is usually less than 10% of the total phospholipids, the greatest concentration being in myelin from brain tissue. However, it may comprise 10 to 20 mol% of the total phospholipid in the plasma membrane and endoplasmic reticulum of the cell. Phosphatidylserine is an acidic (anionic) phospholipid with three ionizable groups, i.e. the phosphate moiety, the amino group and the carboxyl function. As with other acidic lipids, it exists in nature in salt form, but it has a high propensity to chelate to calcium via the charged oxygen atoms of both the carboxyl and phosphate moieties, modifying the conformation of the polar head group. This interaction may be of considerable relevance to the biological function of phosphatidylserine, especially during bone formation for example. As phosphatidylserine is located entirely on the inner monolayer surface of the plasma membrane (and of other cellular membranes) and it is the most abundant anionic phospholipids. Therefore phosphatidylseriine may make the largest contribution to interfacial effects in membranes involving non-specific electrostatic interactions. This normal distribution is disturbed during platelet activation and cellular apoptosis. In human plasma, 1-stearoyl-2-oleoyl and 1-stearoyl-2-arachidonoyl species predominate, but in brain (especially grey matter), retina and many other tissues 1-stearoyl-2-docosahexaenoyl species are very abundant. Indeed, the ratio of n-3 to n-6 fatty acids in brain phosphatidylserine is very much higher than in most other lipids. While most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. Phosphatidylserines typically carry a net charge of -1 at physiological pH. They mostly have palmitic or stearic acid on carbon 1 and a long chain unsaturated fatty acid (e.g. 18:2, 20:4 and 22:6) on carbon 2. PS biosynthesis involves an exchange reaction of serine for ethanolamine in PE.

Entity Information

DBLinks

Other DBLinks
  • CAS Registry Number: 1446756-47-3
  • CAS Registry Number: 321595-13-5
  • CAS Registry Number: 51446-62-9
  • PubChem: 9547096
  • ChEBI: ChEBI:84519
  • HMDB: HMDB0012378
  • HMDB: HMDB12378
  • LipidMaps: LMGP03010036
  • NCBI MeSH: Phosphatidylserines
  • RefMet: RM0135091
  • Metlin: METLIN_40796
  • Coconut NaturalProduct: CNP0234076.1

Class / Ontology

Metabolic Network
ID EC Number Name
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Organism Source

Taxonomy Source

  1. Homo sapiens [ncbi taxid: 9606]
  2. Mus musculus [ncbi taxid: 10090]
  3. Vitis vinifera [ncbi taxid: 29760]

Pathway Synthetic

pathway id name
PathBank:SMP0001293 phospholipid biosynthesis CL(16:0/16:0/17:0cycw7c/18:1(9Z))
PathBank:SMP0001298 phospholipid biosynthesis CL(16:0/16:0/18:1(9Z)/17:0cycw7c)
PathBank:SMP0001375 phospholipid biosynthesis CL(16:0/18:1(9Z)/16:0/17:0cycw7c)
PathBank:SMP0001380 phospholipid biosynthesis CL(16:0/18:1(9Z)/17:0cycw7c/16:0)
PathBank:SMP0001787 phospholipid biosynthesis (PE(18:0/18:0))
PathBank:SMP0082368 Phosphatidylethanolamine Biosynthesis PE(18:0/18:0)
PathBank:SMP0100320 PathBank:SMP0100320
PathBank:SMP0071420 Phosphatidylethanolamine Biosynthesis PE(18:0/18:0)
PathBank:SMP0071732 Phosphatidylethanolamine Biosynthesis PE(18:0/18:0)
PathBank:SMP0080565 Phosphatidylcholine Biosynthesis PC(18:0/18:0)
PathBank:SMP0086868 Phosphatidylcholine Biosynthesis PC(18:0/18:0)
PathBank:SMP0100197 PathBank:SMP0100197
PathBank:SMP0122069 Phospholipid Biosynthesis CL(18:0/18:0/18:0/18:0)
PathBank:SMP0015205 Phosphatidylethanolamine Biosynthesis PE(18:0/18:0)
PathBank:SMP0070117 Phosphatidylcholine Biosynthesis PC(18:0/18:0)
PathBank:SMP0002517 Lysolipid Incorporation into ER PC(18:0/18:0)
PathBank:SMP0002525 Lysolipid incorporation into Mitochondria PC(18:0/18:0)
PathBank:SMP0087615 Phosphatidylethanolamine Biosynthesis PE(18:0/18:0)
PathBank:SMP0014366 Phosphatidylcholine Biosynthesis PC(18:0/18:0)
PathBank:SMP0063830 Phosphatidylcholine Biosynthesis PC(18:0/18:0)
View All Pathways