RefMet Compound Details

RefMet IDRM0034048
MW structure87964 (View MW Metabolite Database details)
RefMet nameCer 22:0;O3/19:0
Alternative nameCer(t22:0/19:0)
Systematic nameN-(nonadecanoyl)-4R-hydroxydocosasphinganine
SMILESCCCCCCCCCCCCCCCCCC[C@H]([C@H]([C@H](CO)NC(=O)CCCCCCCCCCCCCCCCCC)O)O   Run Tanimoto similarity search (with similarity coefficient >=0.6)
Sum CompositionCer 41:0;O3 View other entries in RefMet with this sum composition
Exact mass653.632209 (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
FormulaC41H83NO4View other entries in RefMet with this formula
InChIInChI=1S/C41H83NO4/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-39(44)41(46)38(37-43)42-40(45)36-34-32-30-28-26-24-22-20-18-1
6-14-12-10-8-6-4-2/h38-39,41,43-44,46H,3-37H2,1-2H3,(H,42,45)/t38-,39+,41-/m0/s1
InChIKeyCZEBHFWKUTWYNM-CUVPNIRJSA-NView other enantiomers/diastereomers of this metabolite in RefMet
Super ClassSphingolipids
Main ClassCeramides
Sub ClassPhytoCer (Phytoceramides)
Pubchem CID145715119
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;O3/19:0

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;O3/19:0

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