Castalin

Last updated • a couple of secsFrom Wikipedia, The Free Encyclopedia
Castalin
Chemical structure of castalin Castalin.svg
Chemical structure of castalin
Identifiers
3D model (JSmol)
ChemSpider
PubChem CID
UNII
  • InChI=1S/C27H20O18/c28-2-5-14(31)23-24-20(37)12-11(27(42)45-24)9(18(35)22(39)19(12)36)8-10(26(41)44-23)7(16(33)21(38)17(8)34)6-3(25(40)43-5)1-4(29)13(30)15(6)32/h1,5,14,20,23-24,28-39H,2H2
    Key: PPUHUWSVCUJGTD-UHFFFAOYSA-N
  • C1=C2C(=C(C(=C1O)O)O)C3=C4C(=C(C(=C3O)O)O)C5=C6C(=C(C(=C5O)O)O)C(C(C(C(C(OC2=O)CO)O)OC4=O)OC6=O)O
Properties
C27H20O18
Molar mass 632.439 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Yes check.svgY  verify  (what is  Yes check.svgYX mark.svgN ?)

Castalin is an ellagitannin. It can be found in oak wood [1] and in Melaleuca quinquenervia leaves. [2]

References

  1. ↑ Prida, Andrei; Boulet, Jean-Claude; Ducousso, Alexis; Nepveu, Gérard; Puech, Jean-Louis (2006). "Effect of species and ecological conditions on ellagitannin content in oak wood from an even-aged and mixed stand of Quercus robur L. And Quercus petraea Liebl". Annals of Forest Science. 63 (4): 415–424. Bibcode:2006AnFSc..63..415P. doi:10.1051/forest:2006021. Archived 2007-07-12 at the Wayback Machine
  2. ↑ Moharram, F. A.; Marzouk, M. S.; El-Toumy, S. A. A.; Ahmed, A. A. E.; Aboutabl, E. A. (2003). "Polyphenols of Melaleuca quinquenervia leaves – pharmacological studies of grandinin". Phytotherapy Research. 17 (7): 767–773. doi:10.1002/ptr.1214. PMID   12916075. S2CID   45936055.
This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.