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Myricanone

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Find sources: "Myricanone" – news ·newspapers ·books ·scholar ·JSTOR(August 2024)
Myricanone
Chemical structure of myricanone.
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
  • InChI=1S/C21H24O5/c1-25-20-17-12-14(19(24)21(20)26-2)5-3-4-6-15(22)9-7-13-8-10-18(23)16(17)11-13/h8,10-12,23-24H,3-7,9H2,1-2H3
    Key: ZTSNTUQTNQSIDC-UHFFFAOYSA-N
  • InChI=1/C21H24O5/c1-25-20-17-12-14(19(24)21(20)26-2)5-3-4-6-15(22)9-7-13-8-10-18(23)16(17)11-13/h8,10-12,23-24H,3-7,9H2,1-2H3
    Key: ZTSNTUQTNQSIDC-UHFFFAOYAU
  • COC1=C(C(=C2CCCCC(=O)CCC3=CC(=C(C=C3)O)C1=C2)O)OC
Properties
C21H24O5
Molar mass356.41 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Myricanone is a cyclicdiarylheptanoid isolated from the bark ofMyrica rubra (Myricaceae).[1]

References

[edit]
  1. ^Akazawa, H; Fujita, Y; Banno, N; Watanabe, K; Kimura, Y; Manosroi, A; Manosroi, J; Akihisa, T (2010)."Three new cyclic diarylheptanoids and other phenolic compounds from the bark of Myrica rubra and their melanogenesis inhibitory and radical scavenging activities".Journal of Oleo Science.59 (4):213–221.doi:10.5650/jos.59.213.PMID 20299768.
Types of naturaldiarylheptanoids
Linear
Cyclic
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