Hispidulin

Hispidulin
Names
IUPAC name
4′,5,7-Trihydroxy-6-methoxyflavone
Systematic IUPAC name
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one
Identifiers
CAS Number
  • 1447-88-7 ☒N
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:75902
ChemSpider
  • 4444947
ECHA InfoCard 100.229.713 Edit this at Wikidata
EC Number
  • 802-856-8
KEGG
  • C10058
PubChem CID
  • 5281628
UNII
  • N7F61604C2
CompTox Dashboard (EPA)
  • DTXSID30162786 Edit this at Wikidata
InChI
  • InChI=1S/C16H12O6/c1-21-16-11(19)7-13-14(15(16)20)10(18)6-12(22-13)8-2-4-9(17)5-3-8/h2-7,17,19-20H,1H3
    Key: IHFBPDAQLQOCBX-UHFFFAOYSA-N
  • InChI=1/C16H12O6/c1-21-16-11(19)7-13-14(15(16)20)10(18)6-12(22-13)8-2-4-9(17)5-3-8/h2-7,17,19-20H,1H3
    Key: IHFBPDAQLQOCBX-UHFFFAOYAV
  • COc1c(O)cc2oc(cc(=O)c2c1O)-c1ccc(O)cc1
Properties
Chemical formula
C16H12O6
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Hispidulin is a naturally occurring flavone with potential antiepileptic activity in rats and gerbils.[1][2] It is found in plants including Grindelia argentina, Arrabidaea chica, Saussurea involucrate, Crossostephium chinense, Artemisia, and Salvia.[3]

Complementary medicine

In traditional and complementary medicine it is claimed to have "antioxidant, antifungal, anti-inflammatory, antimutagenic, and antineoplastic properties".[3]

Notes

  1. ^ Hispidulin inhibits the release of glutamate in rat cerebrocortical nerve terminals. Lin TY1, Lu CW, Wang CC, Lu JF, Wang SJ. Toxicol Appl Pharmacol. 2012 Sep 1;263(2):233-43. doi: 10.1016/j.taap.2012.06.015. Epub 2012 Jul 1.
  2. ^ The flavone hispidulin, a benzodiazepine receptor ligand with positive allosteric properties, traverses the blood–brain barrier and exhibits anticonvulsive effects, Dominique Kavvadias et al, British Journal of Pharmacology (2004) 142, 811–820
  3. ^ a b Kanika Patel, Dinesh Kumar Patel, Medicinal importance, pharmacological activities, and analytical aspects of hispidulin: A concise report, Journal of Traditional and Complementary Medicine, 2016, ISSN 2225-4110, https://dx.doi.org/10.1016/j.jtcme.2016.11.003.


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Flavones and their conjugates
Aglycones
Monohydroxyflavone
Dihydroxyflavones
Trihydroxyflavones
Tetrahydroxyflavones
Pentahydroxyflavones
O-methylated flavones
Glycosides
of apigenin
of baicalein
of hypolaetin
  • Hypolaetin 8-glucoside
  • Hypolaetin 8-glucuronide
of luteolin
Acetylated
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    • MRK-409 (MK-0343)
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    See also: Receptor/signaling modulators • GABA receptor modulators • GABA metabolism/transport modulators


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