Cannabis Ruderalis

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6-Methylapigenin
Names
IUPAC name
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methylchromen-4-one
Identifiers
3D model (JSmol)
  • InChI=1S/C16H12O5/c1-8-11(18)6-14-15(16(8)20)12(19)7-13(21-14)9-2-4-10(17)5-3-9/h2-7,17-18,20H,1H3
  • CC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O
Properties
C16H12O5
Molar mass 284.267 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

6-Methylapigenin is a naturally occurring flavonoid and a derivative of Apigenin. It has activity at GABAA receptors as a positive modulator.

Natural occurrence[edit]

6-Methylapigenin can be found in multiple plants, such as Valeriana officinalis, Valeriana jatamansi, and Picea neoveitchii.[1]

Biological activity[edit]

6-Methylapigenin binds to the GABAA receptor on the benzodiazepine binding site. This compound possesses anxiolytic effects, it is also able to potentiate sleep induced by hesperidin, another flavonoid.[2][3] However, it does not have the chemical structure of benzodiazepines, it can therefore be classed as a nonbenzodiazepine.

References[edit]

  1. ^ PubChem. "6-Methylapigenin". pubchem.ncbi.nlm.nih.gov. Retrieved 2024-02-04.
  2. ^ Fernández, Sebastián P.; Wasowski, Cristina; Paladini, Alejandro C.; Marder, Mariel (2005-04-11). "Synergistic interaction between hesperidin, a natural flavonoid, and diazepam". European Journal of Pharmacology. 512 (2–3): 189–198. doi:10.1016/j.ejphar.2005.02.039. ISSN 0014-2999. PMID 15840404.
  3. ^ Marder, Mariel; Viola, Haydeé; Wasowski, Cristina; Fernández, Sebastián; Medina, Jorge H.; Paladini, Alejandro C. (2003). "6-methylapigenin and hesperidin: new valeriana flavonoids with activity on the CNS". Pharmacology, Biochemistry, and Behavior. 75 (3): 537–545. doi:10.1016/s0091-3057(03)00121-7. ISSN 0091-3057. PMID 12895671. S2CID 37559366.
source: https://en.wikipedia.org/w/index.php?title=6-Methylapigenin&action=edit&redlink=1

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