CHEBI:16893 - sphinganine 1-phosphate

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
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 XML SDF
more structures >>
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
(2S,3R)-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 Waiting for 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