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Aviculin

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Aviculin
Names
IUPAC name methyl α-L-rhamnopyranoside
Systematic IUPAC name (2R,3R,4R,5R,6S)-2-{methoxy}-6-methyloxane-3,4,5-triol
Other names isolariciresinol-9'-rhamnopyranoside
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C26H34O10/c1-12-23(30)24(31)25(32)26(36-12)35-11-17-15(10-27)6-14-8-21(34-3)19(29)9-16(14)22(17)13-4-5-18(28)20(7-13)33-2/h4-5,7-9,12,15,17,22-32H,6,10-11H2,1-3H3/t12-,15-,17-,22-,23-,24+,25+,26+/m0/s1Key: FPJFPMQEUVMUKU-CDDCGRQRSA-N
SMILES
  • C1((((O1)OC2(CC3=CC(=C(C=C32C4=CC(=C(C=C4)O)OC)O)OC)CO)O)O)O
Properties
Chemical formula C26H34O10
Molar mass 506.54 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Aviculin is a lignan. It is bio-active isolate of Pseudocydonia sinensis or Polygonum aviculare.

References

  1. "KNApSAcK Metabolite Information - C00031615". www.knapsackfamily.com.
  2. Gao H, Wu L, Kuroyanagi M, Harada K, Kawahara N, Nakane T, Umehara K, Hirasawa A, Nakamura Y (November 2003). "Antitumor-promoting constituents from Chaenomeles sinensis KOEHNE and their activities in JB6 mouse epidermal cells". Chem. Pharm. Bull. 51 (11): 1318–21. doi:10.1248/cpb.51.1318. PMID 14600382.
  3. Ja Kim, Hyoung (1994). "A Novel Lignan and Flavonoids from Polygonum aviculare". Journal of Natural Products. 57 (5): 581–586. doi:10.1021/np50107a003.


Types of lignans
Lignans
Lignan glycosides
Mammalian lignans (enterolignans)
Neolignans
Flavonolignans


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