Syringaresinol
-Syringaresinol.svg)
| |
| 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 | |
PubChem CID
|
|
| UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
| 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]- ^ 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.
- ^ 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.
 | This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |