Produktinformation
- (1R,3R,4R,6S,9S)-9-[(Benzoyloxy)methyl]-1-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-4-hydroxy-6-methyl-7-oxatricyclo[4.3.0.0<sup>3,9</sup>]nonan-8-one
- 7-Oxatricyclo[4.3.0.0<sup>3,9</sup>]nonan-8-one, 9-[(benzoyloxy)methyl]-1-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-4-hydroxy-6-methyl-, (1R,3R,4R,6S,9S)-
- Alibiflorin
- [(1R,4R,6S)-1-(beta-D-glucopyranosyloxy)-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0~3,9~]non-9-yl]methyl benzoate
- [1-(beta-D-glucopyranosyloxy)-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0~3,9~]non-9-yl]methyl benzoate
- 7-Oxatricyclo[4.3.0.03,9]nonan-8-one, 9-[(benzoyloxy)methyl]-1-(β-D-glucopyranosyloxy)-4-hydroxy-6-methyl-, (1R,3R,4R,6S,9S)-
- (1R,3R,4R,6S,9S)-9-[(Benzoyloxy)methyl]-1-(β-D-glucopyranosyloxy)-4-hydroxy-6-methyl-7-oxatricyclo[4.3.0.03,9]nonan-8-one
Albiflorin is a natural phenolic compound that has been shown to be an inhibitor of toll-like receptor (TLR) 4. In vitro experiments have shown that albiflorin can modulate the TLR-induced inflammatory response by inhibiting the production of proinflammatory cytokines, such as IL-6, IL-8, and TNF-α. This compound also inhibits matrix metalloproteinase activity in tubulointerstitial injury, leading to decreased interstitial inflammation and proteinuria. Albiflorin has been shown to be effective at low doses in experimental models of rheumatoid arthritis. It is believed that this effect may be due to its ability to inhibit TLR4 expression or activation.
Chemische Eigenschaften
Technische Anfrage zu: 3D-OA10410 Albiflorin
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