Jump to content

Syringaresinol

From Wikipedia, the free encyclopedia
Syringaresinol
Syringaresinol
Names
IUPAC name
(7α,7′α,8α,8′α)-3,3′,5,5′-Tetramethoxy-7,9′:7′,9-diepoxylignane-4,4′-diol
Systematic IUPAC name
4,4′-[(1R,3aS,4R,6aS)-Tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl]bis(2,6-dimethoxyphenol)
Other names
(+)-Syringaresinol
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
KEGG
UNII
  • InChI=1S/C22H26O8/c1-25-15-5-11(6-16(26-2)19(15)23)21-13-9-30-22(14(13)10-29-21)12-7-17(27-3)20(24)18(8-12)28-4/h5-8,13-14,21-24H,9-10H2,1-4H3/t13-,14-,21+,22+/m0/s1
    Key: KOWMJRJXZMEZLD-HCIHMXRSSA-N
  • O4[C@H](c1cc(OC)c(O)c(OC)c1)[C@@H]2[C@@H]([C@H](OC2)c3cc(OC)c(O)c(OC)c3)C4
Properties
C22H26O8
Molar mass 418.442 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Syringaresinol is a lignan found in Castela emoryi,[1] in Prunus mume.[2]

This compound inhibits Helicobacter pylori motility in vitro.[2]

References

[edit]
  1. ^ Stöcklin, W.; De Silva, L.B.; Geissman, T.A. (1969). "Constituents of holacantha emoryi". Phytochemistry. 8 (8): 1565. Bibcode:1969PChem...8.1565S. doi:10.1016/S0031-9422(00)85931-2.
  2. ^ a b Miyazawa, M; Utsunomiya, H; Inada, K; Yamada, T; Okuno, Y; Tanaka, H; Tatematsu, M (2006). "Inhibition of Helicobacter pylori motility by (+)-Syringaresinol from unripe Japanese apricot". Biological & Pharmaceutical Bulletin. 29 (1): 172–3. doi:10.1248/bpb.29.172. PMID 16394533.


pFad - Phonifier reborn

Pfad - The Proxy pFad of © 2024 Garber Painting. All rights reserved.

Note: This service is not intended for secure transactions such as banking, social media, email, or purchasing. Use at your own risk. We assume no liability whatsoever for broken pages.


Alternative Proxies:

Alternative Proxy

pFad Proxy

pFad v3 Proxy

pFad v4 Proxy