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ChEBI
> Main
CHEBI:52374 -
N
-(2-hydroxyhexacosanyl)-(4
R
)-phytosphingosine
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ChEBI Name
N
-(2-hydroxyhexacosanyl)-(4
R
)-phytosphingosine
ChEBI ID
CHEBI:52374
ChEBI ASCII Name
N-(2-hydroxyhexacosanyl)-(4R)-phytosphingosine
Definition
An
N
-(2-hydroxyhexacosanoyl)phytosphingosine in which the 4-hydroxy group on the phytosphingosine portion has
R
-configuration.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
kieran
Supplier Information
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Formula
C44H89NO5
Net Charge
0
Average Mass
712.18120
Monoisotopic Mass
711.67407
InChI
InChI=1S/C44H89NO5/c1-
3-
5-
7-
9-
11-
13-
15-
17-
18-
19-
20-
21-
22-
23-
24-
25-
26-
28-
30-
32-
34-
36-
38-
42(48)
44(50)
45-
40(39-
46)
43(49)
41(47)
37-
35-
33-
31-
29-
27-
16-
14-
12-
10-
8-
6-
4-
2/h40-
43,46-
49H,3-
39H2,1-
2H3,(H,45,50)
/t40-
,41+,42?,43-
/m0/s1
InChIKey
XNLFLZXNXQVPII-YIWOKQJZSA-N
SMILES
CCCCCCCCCCCCCCCCCCCCCCCCC(O)C(=O)N[C@@H](CO)[C@H](O)[C@H](O)CCCCCCCCCCCCCC
Metabolite of Species
Details
Saccharomyces cerevisiae
(NCBI:txid4932)
Source: yeast.sf.net See:
PubMed
Roles Classification
Biological Role
(s):
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (
Saccharomyces cerevisiae
).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
(via
N-acylphytosphingosine
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
N
-(2-hydroxyhexacosanyl)-(4
R
)-phytosphingosine (
CHEBI:52374
)
has role
Saccharomyces cerevisiae
metabolite (
CHEBI:75772
)
N
-(2-hydroxyhexacosanyl)-(4
R
)-phytosphingosine (
CHEBI:52374
)
is a
N
-(2-hydroxyhexacosanoyl)phytosphingosine (
CHEBI:64958
)
IUPAC Name
2-hydroxy-
N
-[(2
S
,3
S
,4
R
)-1,3,4-trihydroxyoctadecan-2-yl]hexacosanamide
Synonyms
Sources
Cer(t18:0/26:0(2-OH))
LIPID MAPS
cer3_26
ChEBI
ceramide-3 (phytosphingosine:
N
-
C
26:
2
OH)
ChEBI
N
-(2-hydroxyhexacosanoyl)-4
R
-hydroxysphinganine
LIPID MAPS
N
-(2-hydroxyhexacosanoyl)-phytoceramide
LIPID MAPS
N
-(2-hydroxyhexacosanyl)-(4
R
)-hydroxysphinganine
UniProt
Manual Xref
Database
LMSP02030003
LIPID MAPS
View more database links
Registry Number
Type
Source
8821426
Reaxys Registry Number
Reaxys
Last Modified
06 December 2017