CHEBI:17270 - glycerol 2-phosphate

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ChEBI Name glycerol 2-phosphate
ChEBI ID CHEBI:17270
Definition A glycerol monophosphate having the phosphate group at the 2-position.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:14337, CHEBI:42620, CHEBI:5451, CHEBI:26704
Supplier Information
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Formula C3H9O6P
Net Charge 0
Average Mass 172.07372
Monoisotopic Mass 172.01368
InChI InChI=1S/C3H9O6P/c4-1-3(2-5)9-10(6,7)8/h3-5H,1-2H2,(H2,6,7,8)
InChIKey DHCLVCXQIBBOPH-UHFFFAOYSA-N
SMILES OCC(CO)OP(O)(O)=O
Metabolite of Species Details
Chlamydomonas reinhardtii (NCBI:txid3055) See: PubMed
Arabidopsis thaliana (NCBI:txid3702) See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Roles Classification
Biological Role(s): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing glycerol 2-phosphate (CHEBI:17270) has role Escherichia coli metabolite (CHEBI:76971)
glycerol 2-phosphate (CHEBI:17270) has role plant metabolite (CHEBI:76924)
glycerol 2-phosphate (CHEBI:17270) is a glycerol monophosphate (CHEBI:16890)
glycerol 2-phosphate (CHEBI:17270) is conjugate acid of glycerol 2-phosphate(2−) (CHEBI:58083)
Incoming glycerol 2-phosphate(2−) (CHEBI:58083) is conjugate base of glycerol 2-phosphate (CHEBI:17270)
IUPAC Name
glycerol 2-(dihydrogen phosphate)
Synonyms Sources
1,2,3-propanetriol, 2-(dihydrogen phosphate) ChemIDplus
1,3-hydroxy-2-propyl dihydrogen phosphate ChemIDplus
2-glycerophosphate ChEBI
2-HYDROXY-1-(HYDROXYMETHYL)ETHYL DIHYDROGEN PHOSPHATE PDBeChem
β-glycerophosphate ChEBI
β-glycerophosphoric acid ChemIDplus
Glycerol 2-phosphate KEGG COMPOUND
Manual Xrefs Databases
C00007407 KNApSAcK
C02979 KEGG COMPOUND
CPD-536 MetaCyc
DB01779 DrugBank
G2H PDBeChem
View more database links
Registry Numbers Types Sources
1706815 Reaxys Registry Number Reaxys
17181-54-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10952545 PubMed citation Europe PMC
19429609 PubMed citation Europe PMC
22770225 PubMed citation Europe PMC
6083437 PubMed citation Europe PMC
Last Modified
14 December 2016