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Aviculin

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Aviculin
Names
Other names
Identifiers
3D model (JSmol)
ChemSpider
  • 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/s1
    Key: FPJFPMQEUVMUKU-CDDCGRQRSA-N
  • C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@H]2[C@@H](CC3=CC(=C(C=C3[C@@H]2C4=CC(=C(C=C4)O)OC)O)OC)CO)O)O)O
Properties
C26H34O10
Molar mass 506.54 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Aviculin is a lignan. It is bio-active isolate of Pseudocydonia sinensis[1] or Polygonum aviculare.[2]

References

  1. ^ Gao, H; Wu, L; Kuroyanagi, M; et al. (November 2003). "Antitumor-promoting constituents from Chaenomeles sinensis KOEHNE and their activities in JB6 mouse epidermal cells". Chem. Pharm. Bull. 51: 1318–21. doi:10.1248/cpb.51.1318. PMID 14600382. {{cite journal}}: Explicit use of et al. in: |last4= (help)
  2. ^ Ja Kim, Hyoung (1994). "A Novel Lignan and Flavonoids from Polygonum aviculare". Journal of Natural Products. 57: 581–586. doi:10.1021/np50107a003.



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