CHEBI:17436 - (R)-5-phosphomevalonic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (R)-5-phosphomevalonic acid
ChEBI ID CHEBI:17436
ChEBI ASCII Name (R)-5-phosphomevalonic acid
Definition A carboxyalkyl phosphate that is mevalonic acid phosphorylated at position 5.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:10991, CHEBI:10990, CHEBI:18675, CHEBI:333
Supplier Information
Download Molfile XML SDF
Formula C6H13O7P
Net Charge 0
Average Mass 228.13698
Monoisotopic Mass 228.03989
InChI InChI=1S/C6H13O7P/c1-6(9,4-5(7)8)2-3-13-14(10,11)12/h9H,2-4H2,1H3,(H,7,8)(H2,10,11,12)/t6-/m1/s1
InChIKey OKZYCXHTTZZYSK-ZCFIWIBFSA-N
SMILES C[C@@](O)(CCOP(O)(O)=O)CC(O)=O
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Roles Classification
Chemical Role(s): 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).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (R)-5-phosphomevalonic acid (CHEBI:17436) has functional parent (R)-mevalonic acid (CHEBI:17710)
(R)-5-phosphomevalonic acid (CHEBI:17436) has role mouse metabolite (CHEBI:75771)
(R)-5-phosphomevalonic acid (CHEBI:17436) is a carboxyalkyl phosphate (CHEBI:36952)
(R)-5-phosphomevalonic acid (CHEBI:17436) is a primary alcohol (CHEBI:15734)
(R)-5-phosphomevalonic acid (CHEBI:17436) is conjugate acid of (R)-5-phosphonatomevalonate(3−) (CHEBI:58146)
Incoming (R)-5-phosphonatomevalonate(3−) (CHEBI:58146) is conjugate base of (R)-5-phosphomevalonic acid (CHEBI:17436)
IUPAC Name
(3R)-3-hydroxy-3-methyl-5-(phosphonooxy)pentanoic acid
Synonyms Sources
(R)-5-Phosphomevalonate KEGG COMPOUND
(R)-5-phosphomevalonate ChEBI
(R)-5-Phosphomevaloonic acid KEGG COMPOUND
(R)-Mevalonic acid 5-phosphate KEGG COMPOUND
Manual Xrefs Databases
C00007304 KNApSAcK
C01107 KEGG COMPOUND
PMV PDBeChem
View more database links
Last Modified
23 March 2023