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> Main
CHEBI:16893 - sphinganine 1-phosphate
Main
ChEBI Ontology
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ChEBI Name
sphinganine 1-phosphate
ChEBI ID
CHEBI:16893
Definition
A sphingoid 1-phosphate that is the monophosphorylated derivative of sphinganine.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:9222, CHEBI:15100, CHEBI:23767
Supplier Information
Download
Molfile
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Molfile
Formula
C18H40NO5P
Net Charge
0
Average Mass
381.48770
Monoisotopic Mass
381.26441
InChI
InChI=1S/C18H40NO5P/c1-
2-
3-
4-
5-
6-
7-
8-
9-
10-
11-
12-
13-
14-
15-
18(20)
17(19)
16-
24-
25(21,22)
23/h17-
18,20H,2-
16,19H2,1H3,(H2,21,22,23)
/t17-
,18+/m0/s1
InChIKey
YHEDRJPUIRMZMP-ZWKOTPCHSA-N
SMILES
CCCCCCCCCCCCCCC[C@@H](O)[C@@H](N)COP(O)(O)=O
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
See:
MetaboLights Study
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Homo sapiens
(NCBI:txid9606)
Found in blood
(UBERON:0000178)
. See:
PubMed
Homo sapiens
(NCBI:txid9606)
From MetaboLights See:
MetaboLights Study
Roles Classification
Biological Role
(s):
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
sphinganine 1-phosphate (
CHEBI:16893
)
has functional parent
sphinganine (
CHEBI:16566
)
sphinganine 1-phosphate (
CHEBI:16893
)
has role
mouse metabolite (
CHEBI:75771
)
sphinganine 1-phosphate (
CHEBI:16893
)
is a
sphingoid 1-phosphate (
CHEBI:77068
)
sphinganine 1-phosphate (
CHEBI:16893
)
is conjugate acid of
sphinganine 1-phosphate(1−) (
CHEBI:57939
)
Incoming
sphinganine 1-phosphate(1−) (
CHEBI:57939
)
is conjugate base of
sphinganine 1-phosphate (
CHEBI:16893
)
IUPAC Name
sphinganine 1-(dihydrogen phosphate)
Synonyms
Sources
(2
S
,3
R
)-2-amino-3-hydroxyoctadecyl dihydrogen phosphate
IUPAC
DHS-1P
ChEBI
DHS1P
ChEBI
Dihydrosphingosine 1-phosphate
KEGG COMPOUND
dihydrosphingosine-1-phosphate
ChemIDplus
Sphinganine 1-phosphate
KEGG COMPOUND
Manual Xrefs
Databases
C00007541
KNApSAcK
C01120
KEGG COMPOUND
FDB022594
FooDB
HMDB0001383
HMDB
LMSP01050002
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
19794-97-9
CAS Registry Number
ChemIDplus
6780476
Reaxys Registry Number
Reaxys
Citations
Types
Sources
16278291
PubMed citation
Europe PMC
16529909
PubMed citation
Europe PMC
17060094
PubMed citation
Europe PMC
18482992
PubMed citation
Europe PMC
19119142
PubMed citation
Europe PMC
20309867
PubMed citation
Europe PMC
22016110
PubMed citation
Europe PMC
23373542
PubMed citation
Europe PMC
2754341
PubMed citation
Europe PMC
27585475
PubMed citation
Europe PMC
30557628
PubMed citation
Europe PMC
32278008
PubMed citation
Europe PMC
33535437
PubMed citation
Europe PMC
7897327
PubMed citation
Europe PMC
8192648
PubMed citation
Europe PMC
9353337
PubMed citation
Europe PMC
Last Modified
19 January 2022