CHEBI:155863 - 2,4-dihydroxy-6-methylbenzaldehyde

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 2,4-dihydroxy-6-methylbenzaldehyde
ChEBI ID CHEBI:155863
Definition A dihydroxybenzaldehyde that is 2,4-dihydroxybenzaldehyde in which the hydrogen at position 6 has been replaced by a methyl group. It is a fungal metabolite isolated from Grifola frondosa and Phlebiopsis gigantea.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Kristian Axelsen
Supplier Information
Download Molfile XML SDF
Formula C8H8O3
Net Charge 0
Average Mass 152.149
Monoisotopic Mass 152.04734
InChI InChI=1S/C8H8O3/c1-5-2-6(10)3-8(11)7(5)4-9/h2-4,10-11H,1H3
InChIKey LJFQTUKKYWDRAT-UHFFFAOYSA-N
SMILES C=1(C=C(C(=C(C1)O)C(=O)[H])C)O
Metabolite of Species Details
Grifola frondosa (NCBI:txid5627) Found in cell suspension culture (BTO:0000221). See: PubMed
Phlebiopsis gigantea (NCBI:txid82310) Found in cell suspension culture (BTO:0000221). See: PubMed
Roles Classification
Biological Role(s): apoptosis inducer
Any substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms.
fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
Application(s): anti-inflammatory agent
Any compound that has anti-inflammatory effects.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2,4-dihydroxy-6-methylbenzaldehyde (CHEBI:155863) has role anti-inflammatory agent (CHEBI:67079)
2,4-dihydroxy-6-methylbenzaldehyde (CHEBI:155863) has role apoptosis inducer (CHEBI:68495)
2,4-dihydroxy-6-methylbenzaldehyde (CHEBI:155863) has role fungal metabolite (CHEBI:76946)
2,4-dihydroxy-6-methylbenzaldehyde (CHEBI:155863) is a dihydroxybenzaldehyde (CHEBI:50196)
IUPAC Name
2,4-dihydroxy-6-methylbenzaldehyde
Synonyms Sources
2-formyl-5-hydroxy-3-methylphenol ChemIDplus
2-methyl-4,6-dihydroxybenzaldehyde ChEBI
4-formyl-5-methylbenzene-1,3-diol ChemIDplus
4-formyl-5-methylresorcinol ChemIDplus
6-methyl-β-resorcyladehyde ChemIDplus
o-orsellinaldehyde ChemIDplus
orcinaldehyde ChemIDplus
orcylaldehyde ChemIDplus
orsellinaldehyde UniProt
Registry Number Type Source
487-69-4 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
17002422 PubMed citation Europe PMC
22510154 PubMed citation SUBMITTER
29867500 PubMed citation Europe PMC
29895730 PubMed citation Europe PMC
30269491 PubMed citation Europe PMC
883459 PubMed citation Europe PMC
Last Modified
16 June 2020