ChEBI

CHEBI:68701 - (E)-5-hydroxy-6-(3-methylbut-2-enyl)-2-(pent-1-enyl)benzofuran-4-carbaldehyde

ChEBI Name (E)-5-hydroxy-6-(3-methylbut-2-enyl)-2-(pent-1-enyl)benzofuran-4-carbaldehyde ChEBI ID CHEBI:68701 ChEBI ASCII Name (E)-5-hydroxy-6-(3-methylbut-2-enyl)-2-(pent-1-enyl)benzofuran-4-carbaldehyde Definition A member of the class of 1-benzofurans that is 1-benzofuran substituted by a hydroxy group at position 5, a prenyl group at position 6 and a pent-1-en-1-yl group at position 2. Isolated from Chaetomium globosum, it exhibits radical scavenging activity. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:68192 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 C19H22O3 Net Charge 0 Average Mass 298.37620 Monoisotopic Mass 298.15689 InChI InChI=1S/C19H22O3/c1-4-5-6-7-15-11-16-17(12-20)19(21)14(9-8-13(2)3)10-18(16)22-15/h6-8,10-12,21H,4-5,9H2,1-3H3/b7-6+ InChIKey SBYYFNVKZGJIPR-VOTSOKGWSA-N SMILES CCC\C=C\c1cc2c(C=O)c(O)c(CC=C(C)C)cc2o1 Metabolite of Species Details Chaetomium globosum (NCBI:txid38033) See: PubMed Aspergillus cristatus (NCBI:txid573508) of strain CB10006 See: DOI Eurotium repens (NCBI:txid41409) EtOAc extract of Lyophilized fungus which was homogenized with acetone See: PubMed Roles Classification Chemical Role(s): radical scavenger A role played by a substance that can react readily with, and thereby eliminate, radicals. Biological Role(s): Chaetomium metabolite Any fungal metabolite produced during a metabolic reaction in the mould, Chaetomium. Aspergillus metabolite Any fungal metabolite produced during a metabolic reaction in the mould, Aspergillus . View more via ChEBI Ontology ChEBI Ontology Outgoing (E)-5-hydroxy-6-(3-methylbut-2-enyl)-2-(pent-1-enyl)benzofuran-4-carbaldehyde (CHEBI:68701) has role Aspergillus metabolite (CHEBI:76956) (E)-5-hydroxy-6-(3-methylbut-2-enyl)-2-(pent-1-enyl)benzofuran-4-carbaldehyde (CHEBI:68701) has role Chaetomium metabolite (CHEBI:76960) (E)-5-hydroxy-6-(3-methylbut-2-enyl)-2-(pent-1-enyl)benzofuran-4-carbaldehyde (CHEBI:68701) has role radical scavenger (CHEBI:48578) (E)-5-hydroxy-6-(3-methylbut-2-enyl)-2-(pent-1-enyl)benzofuran-4-carbaldehyde (CHEBI:68701) is a 1-benzofurans (CHEBI:38830) (E)-5-hydroxy-6-(3-methylbut-2-enyl)-2-(pent-1-enyl)benzofuran-4-carbaldehyde (CHEBI:68701) is a aldehyde (CHEBI:17478) (E)-5-hydroxy-6-(3-methylbut-2-enyl)-2-(pent-1-enyl)benzofuran-4-carbaldehyde (CHEBI:68701) is a phenols (CHEBI:33853) IUPAC Name 5-hydroxy-6-(3-methylbut-2-en-1-yl)-2-[(1E)-pent-1-en-1-yl]-1-benzofuran-4-carbaldehyde Synonyms Sources 2-(2',3-epoxy-1',3'-heptadienyl)-6-hydroxy-5-(3-methyl-2-butenyl)benzaldehyde Note: (2021-04-12) synonym obtained from PMID:17125234 but is incorrect. ChEBI 5-hydroxy-6-(3-methylbut-2-enyl)-2-[(E)-pent-1-enyl]-1-benzofuran-4-carbaldehyde ChEBI Manual Xrefs Databases 23326592 ChemSpider C00029427 KNApSAcK View more database links Registry Numbers Types Sources 15811804 Reaxys Registry Number Reaxys 916602-30-7 CAS Registry Number PubChem Citations Types Sources 17125234 PubMed citation Europe PMC 21667972 PubMed citation Europe PMC 23024574 PubMed citation Europe PMC Last Modified 12 April 2021