CHEBI:142801 - 3,6,7,9-tetrahydroxy-3-methyl-2,3-dihydro-1H-naphtho[2,1-b]pyran-1-one

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ChEBI Name 3,6,7,9-tetrahydroxy-3-methyl-2,3-dihydro-1H-naphtho[2,1-b]pyran-1-one
ChEBI ID CHEBI:142801
ChEBI ASCII Name 3,6,7,9-tetrahydroxy-3-methyl-2,3-dihydro-1H-naphtho[2,1-b]pyran-1-one
Definition A naphtho-γ-pyrone that is 3-methyl-2,3-dihydro-1H-naphtho[2,1-b]pyran-1-one substituted by hydroxy groups at positions 3,6,7 and 9.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Anne Morgat
Supplier Information
Download Molfile XML SDF
Formula C14H12O6
Net Charge 0
Average Mass 276.244
Monoisotopic Mass 276.06339
InChI InChI=1S/C14H12O6/c1-14(19)5-10(18)13-7-2-6(15)3-8(16)12(7)9(17)4-11(13)20-14/h2-4,15-17,19H,5H2,1H3
InChIKey XHAKGHGCOBKEEK-UHFFFAOYSA-N
SMILES C1=C(C2=C(C3=C1OC(CC3=O)(O)C)C=C(C=C2O)O)O
ChEBI Ontology
Outgoing 3,6,7,9-tetrahydroxy-3-methyl-2,3-dihydro-1H-naphtho[2,1-b]pyran-1-one (CHEBI:142801) is a cyclic hemiketal (CHEBI:59780)
3,6,7,9-tetrahydroxy-3-methyl-2,3-dihydro-1H-naphtho[2,1-b]pyran-1-one (CHEBI:142801) is a heptaketide (CHEBI:59872)
3,6,7,9-tetrahydroxy-3-methyl-2,3-dihydro-1H-naphtho[2,1-b]pyran-1-one (CHEBI:142801) is a naphtho-γ-pyrone (CHEBI:64542)
3,6,7,9-tetrahydroxy-3-methyl-2,3-dihydro-1H-naphtho[2,1-b]pyran-1-one (CHEBI:142801) is a phenols (CHEBI:33853)
3,6,7,9-tetrahydroxy-3-methyl-2,3-dihydro-1H-naphtho[2,1-b]pyran-1-one (CHEBI:142801) is conjugate acid of 3,6,7,9-tetrahydroxy-3-methyl-2,3-dihydro-1H-naphtho[2,1-b]pyran-1-one(1−) (CHEBI:142802)
Incoming 3,6,7,9-tetrahydroxy-3-methyl-2,3-dihydro-1H-naphtho[2,1-b]pyran-1-one(1−) (CHEBI:142802) is conjugate base of 3,6,7,9-tetrahydroxy-3-methyl-2,3-dihydro-1H-naphtho[2,1-b]pyran-1-one (CHEBI:142801)
IUPAC Names
3,6,7,9-tetrahydroxy-3-methyl-2,3-dihydro-1H-benzo[f]chromen-1-one
3,6,7,9-tetrahydroxy-3-methyl-2,3-dihydro-1H-naphtho[2,1-b]pyran-1-one
Synonym Source
3,6,7,9-tetrahydroxy-3-methyl-1H,2H,3H-naphtho[2,1-b]pyran-1-one ChEBI
Citation Waiting for Citations Type Source
26978228 PubMed citation SUBMITTER
Last Modified
01 July 2019