CHEBI:28508 - 2,5-dihydroxybenzaldehyde

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name 2,5-dihydroxybenzaldehyde ChEBI ID CHEBI:28508 Definition A dihydroxybenzaldehyde carrying hydroxy groups at positions 2 and 5. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:5322, CHEBI:50203, CHEBI:24217 Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C7H6O3 Net Charge 0 Average Mass 138.12074 Monoisotopic Mass 138.03169 InChI InChI=1S/C7H6O3/c8-4-5-3-6(9)1-2-7(5)10/h1-4,9-10H InChIKey CLFRCXCBWIQVRN-UHFFFAOYSA-N SMILES [H]C(=O)c1cc(O)ccc1O Metabolite of Species Details Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed Penicillium urticae (NCBI:txid29844) See: PubMed Penicillium griseofulvum (NCBI:txid5078) See: PubMed Homo sapiens (NCBI:txid9606) See: DOI Roles Classification Biological Role(s): mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). Penicillium metabolite Any fungal metabolite produced during a metabolic reaction in Penicillium. human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). View more via ChEBI Ontology ChEBI Ontology Outgoing 2,5-dihydroxybenzaldehyde (CHEBI:28508) has role Penicillium metabolite (CHEBI:76964) 2,5-dihydroxybenzaldehyde (CHEBI:28508) has role human metabolite (CHEBI:77746) 2,5-dihydroxybenzaldehyde (CHEBI:28508) has role mouse metabolite (CHEBI:75771) 2,5-dihydroxybenzaldehyde (CHEBI:28508) is a dihydroxybenzaldehyde (CHEBI:50196) IUPAC Name 2,5-dihydroxybenzaldehyde Synonyms Sources 2,5-dihydroxybenzaldehyde UniProt 2,5-Dihydroxybenzaldehyde KEGG COMPOUND gentisaldehyde ChemIDplus Gentisate aldehyde KEGG COMPOUND Manual Xrefs Databases C05585 KEGG COMPOUND CPD-16722 MetaCyc HMDB0004062 HMDB View more database links Registry Numbers Types Sources 1194-98-5 CAS Registry Number ChemIDplus 1194-98-5 CAS Registry Number NIST Chemistry WebBook 1363961 Reaxys Registry Number Reaxys 1363961 Beilstein Registry Number Beilstein 218296 Gmelin Registry Number Gmelin Citations Types Sources 19120654 PubMed citation Europe PMC 241643 PubMed citation Europe PMC 418806 PubMed citation Europe PMC 836020 PubMed citation Europe PMC Last Modified 15 October 2019