Axillarin

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Axillarin
Chemical structure of axillarin
Names
IUPAC name
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,6-dimethoxychromen-4-one
Other names
DMQT
3,6-Dimethoxyquercetagetin
Quercetagetin 3,6-dimethyl ether
3',4',5,7-Tetrahydroxy-3,6-dimethoxyflavone
Identifiers
5188-73-8 N=
ChEBI CHEBI:2941 N
ChEMBL ChEMBL487810 YesY
ChemSpider 4444922 YesY
Jmol 3D model Interactive image
PubChem 5281603
  • InChI=1S/C17H14O8/c1-23-16-10(20)6-11-12(13(16)21)14(22)17(24-2)15(25-11)7-3-4-8(18)9(19)5-7/h3-6,18-21H,1-2H3 YesY
    Key: KIGVXRGRNLQNNI-UHFFFAOYSA-N YesY
  • InChI=1/C17H14O8/c1-23-16-10(20)6-11-12(13(16)21)14(22)17(24-2)15(25-11)7-3-4-8(18)9(19)5-7/h3-6,18-21H,1-2H3
    Key: KIGVXRGRNLQNNI-UHFFFAOYAX
  • COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O
Properties
C17H14O8
Molar mass 346.28 g/mol
Density 1.659 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Axillarin is an O-methylated flavonol. It can be found in Pulicaria crispa, Filifolium sibiricum, Inula britannica,[1] Wyethia bolanderi in Balsamorhiza macrophylla[2] and in Tanacetum vulgare.[3] It can also be synthetized.[4]

Glycosides

Axillarin 7-O-β-D-glucoside can be found in Tagetes mendocina, a medicinal plant widely used in the Andean provinces of Argentina.[5]

References

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