CHEBI:25351 - mevalonic acid

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ChEBI Name mevalonic acid ChEBI ID CHEBI:25351 Definition A racemate composed of equimolar amounts of (R)- and (S)-mevalonic acid. Stars This entity has been manually annotated by the ChEBI Team. Wikipedia License Read full article at Wikipedia Formula C6H12O4 Net Charge 0 Average Mass 148.158 Monoisotopic Mass 148.07356 Metabolite of Species Details Mus musculus (NCBI:txid10090) From MetaboLights See: MetaboLights Study Homo sapiens (NCBI:txid9606) Found in urine (BTO:0001419). See: PubMed Homo sapiens (NCBI:txid9606) Found in blood (UBERON:0000178). See: PubMed C57bl/6 mouse From MetaboLights See: MetaboLights Study Roles Classification Biological Role(s): human urinary metabolite Any metabolite (endogenous or exogenous) found in human urine samples. mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). View more via ChEBI Ontology ChEBI Ontology Outgoing mevalonic acid (CHEBI:25351) has part (R)-mevalonic acid (CHEBI:17710) mevalonic acid (CHEBI:25351) has part (S)-mevalonic acid (CHEBI:28880) mevalonic acid (CHEBI:25351) has role human urinary metabolite (CHEBI:84087) mevalonic acid (CHEBI:25351) has role mouse metabolite (CHEBI:75771) mevalonic acid (CHEBI:25351) is a racemate (CHEBI:60911) mevalonic acid (CHEBI:25351) is conjugate acid of mevalonate (CHEBI:25350) Incoming mevalonolactone (CHEBI:194429) has functional parent mevalonic acid (CHEBI:25351) mevalonyl-CoA (CHEBI:133868) has functional parent mevalonic acid (CHEBI:25351) mevalonate (CHEBI:25350) is conjugate base of mevalonic acid (CHEBI:25351) IUPAC Name rac-3,5-dihydroxy-3-methylpentanoic acid Synonyms Sources (±)-2,4-dideoxy-3-C-methylpentonic acid ChEBI (±)-3,5-dihydroxy-3-methylvaleric acid ChEBI (±)-mevalonic acid ChEBI (±)-MVA ChEBI (3RS)-mevalonic acid ChEBI (RS)-mevalonic acid ChEBI DL-mevalonic acid HMDB rac-mevalonic acid ChEBI rac-MVA ChEBI racemic mevalonic acid ChEBI RS-mevalonic acid HMDB Manual Xrefs Databases HMDB0000227 HMDB Mevalonic_acid Wikipedia View more database links Registry Numbers Types Sources 150-97-0 CAS Registry Number ChemIDplus 1722595 Beilstein Registry Number Beilstein 1722595 Reaxys Registry Number Reaxys Citations Types Sources 10369261 PubMed citation Europe PMC 10647065 PubMed citation Europe PMC 10947201 PubMed citation Europe PMC 11521206 PubMed citation Europe PMC 12031835 PubMed citation Europe PMC 12872277 PubMed citation Europe PMC 1653652 PubMed citation Europe PMC 22770225 PubMed citation Europe PMC 2702744 PubMed citation Europe PMC 3012338 PubMed citation Europe PMC 32004772 PubMed citation Europe PMC 35840187 PubMed citation Europe PMC 36247639 PubMed citation Europe PMC 5683362 PubMed citation Europe PMC 6236250 PubMed citation Europe PMC 6263908 PubMed citation Europe PMC 6565710 PubMed citation Europe PMC 6610447 PubMed citation Europe PMC 6953445 PubMed citation Europe PMC 8747489 PubMed citation Europe PMC Last Modified 23 March 2023