CHEBI:17025 - (S)-dihydroorotic acid

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name (S)-dihydroorotic acid ChEBI ID CHEBI:17025 ChEBI ASCII Name (S)-dihydroorotic acid Definition The (S)-enantiomer of dihydroorotic acid that is an intermediate in the metabolism of pyridine. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:42132, CHEBI:417, CHEBI:18778 Supplier Information ChemicalBook:CB7383339, eMolecules:482145, eMolecules:29536225, eMolecules:29535203, Selleckchem:cholesterol, ZINC000003875383 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C5H6N2O4 Net Charge 0 Average Mass 158.11222 Monoisotopic Mass 158.03276 InChI InChI=1S/C5H6N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h2H,1H2,(H,9,10)(H2,6,7,8,11)/t2-/m0/s1 InChIKey UFIVEPVSAGBUSI-REOHCLBHSA-N SMILES OC(=O)[C@@H]1CC(=O)NC(=O)N1 Metabolite of Species Details Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed Escherichia coli (NCBI:txid562) 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): Escherichia coli metabolite Any bacterial metabolite produced during a metabolic reaction in Escherichia coli. mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). Saccharomyces cerevisiae metabolite Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ). human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). View more via ChEBI Ontology ChEBI Ontology Outgoing (S)-dihydroorotic acid (CHEBI:17025) has role Escherichia coli metabolite (CHEBI:76971) (S)-dihydroorotic acid (CHEBI:17025) has role Saccharomyces cerevisiae metabolite (CHEBI:75772) (S)-dihydroorotic acid (CHEBI:17025) has role human metabolite (CHEBI:77746) (S)-dihydroorotic acid (CHEBI:17025) has role mouse metabolite (CHEBI:75771) (S)-dihydroorotic acid (CHEBI:17025) is a dihydroorotic acid (CHEBI:30865) (S)-dihydroorotic acid (CHEBI:17025) is conjugate acid of (S)-dihydroorotate (CHEBI:30864) (S)-dihydroorotic acid (CHEBI:17025) is enantiomer of (R)-dihydroorotic acid (CHEBI:30866) Incoming (S)-dihydroorotate (CHEBI:30864) is conjugate base of (S)-dihydroorotic acid (CHEBI:17025) (R)-dihydroorotic acid (CHEBI:30866) is enantiomer of (S)-dihydroorotic acid (CHEBI:17025) IUPAC Name (4S)-2,6-dioxohexahydropyrimidine-4-carboxylic acid Synonyms Sources (S)-4,5-dihydroorotic acid ChEBI Dihydro-L-orotic acid KEGG COMPOUND L-Dihydroorotic acid KEGG COMPOUND Manual Xrefs Databases C00007302 KNApSAcK C00337 KEGG COMPOUND DI-H-OROTATE MetaCyc DOR PDBeChem EP0933633 Patent EP1036319 Patent HK1033171 Patent HMDB0003349 HMDB RU2228932 Patent WO9930146 Patent View more database links Registry Numbers Types Sources 1473795 Gmelin Registry Number Gmelin 5988-19-2 CAS Registry Number KEGG COMPOUND 83957 Reaxys Registry Number Reaxys Citation Type Source 3089167 PubMed citation Europe PMC Last Modified 27 January 2016