RefMet Compound Details

RefMet IDRM0124699
MW structure87965 (View MW Metabolite Database details)
RefMet nameCer 22:0;O3/20:0
Alternative nameCer(t22:0/20:0)
Systematic nameN-(eicosanoyl)-4R-hydroxydocosasphinganine
SMILESCCCCCCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@@H]([C@@H](CCCCCCCCCCCCCCCCCC)O)O   Run Tanimoto similarity search (with similarity coefficient >=0.6)
Sum CompositionCer 42:0;O3 View other entries in RefMet with this sum composition
Exact mass667.647859 (neutral)
Calculate m/z:   
View other RefMet entries with this exact (neutral) mass:   +/- 0.05 amu   +/- 0.1 amu   +/- 0.2 amu   +/- 0.5 amu
FormulaC42H85NO4View other entries in RefMet with this formula
InChIInChI=1S/C42H85NO4/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-41(46)43-39(38-44)42(47)40(45)36-34-32-30-28-26-24-22-20-1
8-16-14-12-10-8-6-4-2/h39-40,42,44-45,47H,3-38H2,1-2H3,(H,43,46)/t39-,40+,42-/m0/s1
InChIKeyVRFLRJYZTOVFSY-LFVSMIGWSA-NView other enantiomers/diastereomers of this metabolite in RefMet
Super ClassSphingolipids
Main ClassCeramides
Sub ClassPhytoCer (Phytoceramides)
Pubchem CID145715120
Annotation level1   (1:Known structure; 2:Known regiochemistry; 3:Partial structure; 4:Sum-composition)

Table of KEGG reactions in human pathways involving Cer 22:0;O3/20:0

Rxn IDKEGG ReactionEnzyme
R06526 Dihydroceramide + 2 Ferrocytochrome b5 + Oxygen + 2 H+ <=> Phytoceramide + 2 Ferricytochrome b5 + H2Odihydroceramide,ferrocytochrome b5:oxygen oxidoreductase (C4-hydroxylating)
R06527 C26-CoA + Phytosphingosine <=> CoA + Phytoceramideacyl-CoA: phytosphingosine N-acyltransferase
R06528 Phytoceramide + H2O <=> Fatty acid + PhytosphingosinePhytoceramide amidohydrolase

Table of KEGG human pathways containing Cer 22:0;O3/20:0

Pathway IDHuman Pathway# of reactions
hsa00600 Sphingolipid metabolism 2
hsa01100 Metabolic pathways 1
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