CHEBI:15811 - O-phospho-L-serine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name O-phospho-L-serine
ChEBI ID CHEBI:15811
ChEBI ASCII Name O-phospho-L-serine
Definition The L-enantiomer of O-phosphoserine.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:21966, CHEBI:12718, CHEBI:7692
Supplier Information ChemicalBook:CB0456205, eMolecules:29542138, ZINC000003869280
Download Molfile XML SDF
Wikipedia License
Waiting for wikipedia content
Read full article at Wikipedia
Formula C3H8NO6P
Net Charge 0
Average Mass 185.07252
Monoisotopic Mass 185.00892
InChI InChI=1S/C3H8NO6P/c4-2(3(5)6)1-10-11(7,8)9/h2H,1,4H2,(H,5,6)(H2,7,8,9)/t2-/m0/s1
InChIKey BZQFBWGGLXLEPQ-REOHCLBHSA-N
SMILES N[C@@H](COP(O)(O)=O)C(O)=O
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Saccharomyces cerevisiae (NCBI:txid4932) See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Homo sapiens (NCBI:txid9606) See: DOI
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
EC 1.4.7.1 [glutamate synthase (ferredoxin)] inhibitor
An EC 1.4.* (oxidoreductase acting on donor CH-NH2 group) inhibitor that interferes with the action of any glutamate synthase.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via O-phosphoserine )
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
EC 2.5.1.49 (O-acetylhomoserine aminocarboxypropyltransferase) inhibitor
An EC 2.5.1.* (non-methyl-alkyl or aryl transferase) inhibitor that interferes with the action of O-acetylhomoserine aminocarboxypropyltransferase (EC 2.5.1.49).
EC 4.3.1.10 (serine-sulfate ammonia-lyase) inhibitor
An EC 4.3.1.* (ammonia-lyase) inhibitor that interferes with the action of serine-sulfate ammonia-lyase (EC 4.3.1.10).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing O-phospho-L-serine (CHEBI:15811) has role Escherichia coli metabolite (CHEBI:76971)
O-phospho-L-serine (CHEBI:15811) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
O-phospho-L-serine (CHEBI:15811) has role EC 1.4.7.1 [glutamate synthase (ferredoxin)] inhibitor (CHEBI:62089)
O-phospho-L-serine (CHEBI:15811) has role EC 2.5.1.49 (O-acetylhomoserine aminocarboxypropyltransferase) inhibitor (CHEBI:77089)
O-phospho-L-serine (CHEBI:15811) has role EC 4.3.1.10 (serine-sulfate ammonia-lyase) inhibitor (CHEBI:77090)
O-phospho-L-serine (CHEBI:15811) has role human metabolite (CHEBI:77746)
O-phospho-L-serine (CHEBI:15811) has role mouse metabolite (CHEBI:75771)
O-phospho-L-serine (CHEBI:15811) is a O-phosphoserine (CHEBI:37712)
O-phospho-L-serine (CHEBI:15811) is conjugate acid of O-phosphonato-L-serine(2−) (CHEBI:57524)
O-phospho-L-serine (CHEBI:15811) is enantiomer of O-phospho-D-serine (CHEBI:37713)
Incoming O-phosphonato-L-serine(2−) (CHEBI:57524) is conjugate base of O-phospho-L-serine (CHEBI:15811)
O-phospho-D-serine (CHEBI:37713) is enantiomer of O-phospho-L-serine (CHEBI:15811)
O-phospho-L-serine residue (CHEBI:45522) is substituent group from O-phospho-L-serine (CHEBI:15811)
IUPAC Name
O-phosphono-L-serine
INN Source
dexfosfoserine ChemIDplus
Synonyms Sources
(+)-L-serine dihydrogen phosphate (ester) ChemIDplus
(2S)-2-amino-3-(phosphonooxy)propanoic acid IUPAC
(S)-2-amino-3-hydroxypropanoic acid 3-phosphate ChEBI
3-Phosphoserine KEGG COMPOUND
Dexfosfoserine KEGG COMPOUND
L-O-Phosphoserine KEGG COMPOUND
O-Phospho-L-serine KEGG COMPOUND
O-phosphoserine ChemIDplus
phosphoserine ChEBI
Manual Xrefs Databases
3-P-SERINE MetaCyc
3-phosphoserine Wikipedia
4120 DrugCentral
C00007287 KNApSAcK
C01005 KEGG COMPOUND
EP2444481 Patent
HMDB0000272 HMDB
SEP PDBeChem
View more database links
Registry Numbers Types Sources
1726826 Reaxys Registry Number Reaxys
407-41-0 CAS Registry Number KEGG COMPOUND
407-41-0 CAS Registry Number ChemIDplus
675662 Gmelin Registry Number Gmelin
Citations Waiting for Citations
Last Modified
22 February 2017