CHEBI:17597 - 4-hydroxybenzaldehyde

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ChEBI Name 4-hydroxybenzaldehyde
ChEBI ID CHEBI:17597
Definition A hydroxybenzaldehyde that is benzaldehyde substituted with a hydroxy group at position C-4.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:43009, CHEBI:1857, CHEBI:12002, CHEBI:20396
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Formula C7H6O2
Net Charge 0
Average Mass 122.12134
Monoisotopic Mass 122.03678
InChI InChI=1S/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H
InChIKey RGHHSNMVTDWUBI-UHFFFAOYSA-N
SMILES [H]C(=O)c1ccc(O)cc1
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Pisonia aculeata (NCBI:txid363212) Found in stem (BTO:0001300). Cold methanolic extract of dried stems and roots See: PubMed
Pisonia aculeata (NCBI:txid363212) Found in root (BTO:0001188). Cold methanolic extract of dried stems and roots See: PubMed
Roles Classification
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
EC 1.14.17.1 (dopamine beta-monooxygenase) inhibitor
An EC 1.14.17.* (oxidoreductase acting on paired donors, with incorporation or reduction of molecular oxygen and with reduced ascorbate as one donor, and incorporation of one atom of oxygen) inhibitor that interferes with the action of dopamine monooxygenase (EC 1.14.17.1).
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 4-hydroxybenzaldehyde (CHEBI:17597) has role EC 1.14.17.1 (dopamine β-monooxygenase) inhibitor (CHEBI:139339)
4-hydroxybenzaldehyde (CHEBI:17597) has role mouse metabolite (CHEBI:75771)
4-hydroxybenzaldehyde (CHEBI:17597) has role plant metabolite (CHEBI:76924)
4-hydroxybenzaldehyde (CHEBI:17597) is a hydroxybenzaldehyde (CHEBI:24673)
IUPAC Name
4-hydroxybenzaldehyde
Synonyms Sources
4-formylphenol ChemIDplus
4-Hydroxybenzaldehyde KEGG COMPOUND
4-hydroxybenzaldehyde UniProt
p-formylphenol NIST Chemistry WebBook
p-Hydroxybenzaldehyde KEGG COMPOUND
P-HYDROXYBENZALDEHYDE PDBeChem
Manual Xrefs Databases
4-Hydroxybenzaldehyde Wikipedia
4-HYDROXYBENZALDEHYDE MetaCyc
C00002657 KNApSAcK
C00633 KEGG COMPOUND
c0285 UM-BBD
DB03560 DrugBank
HBA PDBeChem
HMDB0011718 HMDB
View more database links
Registry Numbers Types Sources
123-08-0 CAS Registry Number NIST Chemistry WebBook
123-08-0 CAS Registry Number ChemIDplus
471352 Reaxys Registry Number Reaxys
471352 Beilstein Registry Number Beilstein
82654 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
21542597 PubMed citation Europe PMC
22770225 PubMed citation Europe PMC
3593236 PubMed citation Europe PMC
Last Modified
20 December 2017