D-(-)-水杨苷; D-(-)-水杨甙
D-(-)-Salicin
| 产品名称 |
产品编号 |
CAS编号 |
包装 |
QQ客服 |
| D-(-)-水杨苷; D-(-)-水杨甙 |
CFN99541 |
138-52-3 |
10mg |
QQ客服:1457312923 |
| D-(-)-水杨苷; D-(-)-水杨甙 |
CFN99541 |
138-52-3 |
20mg |
QQ客服:1457312923 |
| D-(-)-水杨苷; D-(-)-水杨甙 |
CFN99541 |
138-52-3 |
50mg |
QQ客服:1457312923 |
| D-(-)-水杨苷; D-(-)-水杨甙 |
CFN99541 |
138-52-3 |
100mg |
QQ客服:1457312923 |
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Cell. 2018 Jan 11;172(1-2):249-261.e12. doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5. doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)PMID: 32004475

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国外学术期刊发表的引用ChemFaces产品的部分文献
Food Analytical Methods2020, 13,1603-1612(2020)
Food Engineering Progress2019, 23(3)209-216
Int J Mol Sci.2024, 25(2):764.
Tropical J. of Pha. Research2017, 16(3):543-552
Phytochem Anal.2022, doi: 10.1002
Evid Based Complement Alternat Med.2017, 2017:7383104
Research Square2023, 2883170.
Viruses2023, 15(6), 1377
| Description: |
D(-)-Salicin is a traditional medicine which has been known to exhibit anti-inflammation and other therapeutic activities, it can inhibit the LPS-induced inflammation in RAW264.7 cells and mouse models. |
| Targets: |
TNF-α | MAPK | NF-kB | IL Receptor |
| In vitro: |
| Int Immunopharmacol. 2015 Jun;26(2):286-94. | | D(-)-Salicin inhibits the LPS-induced inflammation in RAW264.7 cells and mouse models.[Pubmed: 25907238] | D(-)-Salicin is a traditional medicine which has been known to exhibit anti-inflammation and other therapeutic activities.
METHODS AND RESULTS:
The present study aimed to investigate whether D(-)-Salicin inhibited the LPS-induced inflammation in vivo and in vitro. We evaluated the effect of D(-)-Salicin on cytokines (TNF-α, IL-1β, IL-6 and IL-10) in vivo and in vitro by enzyme-linked immunosorbent assay and signaling pathways (MAPKs and NF-κB) in vivo by Western blot. The results showed that D(-)-Salicin markedly decreased TNF-α, IL-1β and IL-6 concentrations and increased IL-10 concentration. In addition, western blot analysis indicated that D(-)-Salicin suppressed the activation of MAPKs and NF-κB signaling pathways stimulated by LPS. To examine whether D(-)-Salicin ameliorated LPS-induced lung inflammation, inhibitors of MAPKs and NF-κB signaling pathways were administrated intraperitoneally to mice. Interference with specific inhibitors revealed that D(-)-Salicin-mediated cytokine suppression was through MAPKs and NF-κB pathways. In the mouse model of acute lung injury, histopathologic examination indicted that D(-)-Salicin suppressed edema induced by LPS.
CONCLUSIONS:
So it is suggest that D(-)-Salicin might be a potential therapeutic agent against inflammatory diseases. |
|
| In vivo: |
| Int Immunopharmacol. 2015 Jun;26(2):286-94. | | D(-)-Salicin inhibits the LPS-induced inflammation in RAW264.7 cells and mouse models.[Pubmed: 25907238] | D(-)-Salicin is a traditional medicine which has been known to exhibit anti-inflammation and other therapeutic activities.
METHODS AND RESULTS:
The present study aimed to investigate whether D(-)-Salicin inhibited the LPS-induced inflammation in vivo and in vitro. We evaluated the effect of D(-)-Salicin on cytokines (TNF-α, IL-1β, IL-6 and IL-10) in vivo and in vitro by enzyme-linked immunosorbent assay and signaling pathways (MAPKs and NF-κB) in vivo by Western blot. The results showed that D(-)-Salicin markedly decreased TNF-α, IL-1β and IL-6 concentrations and increased IL-10 concentration. In addition, western blot analysis indicated that D(-)-Salicin suppressed the activation of MAPKs and NF-κB signaling pathways stimulated by LPS. To examine whether D(-)-Salicin ameliorated LPS-induced lung inflammation, inhibitors of MAPKs and NF-κB signaling pathways were administrated intraperitoneally to mice. Interference with specific inhibitors revealed that D(-)-Salicin-mediated cytokine suppression was through MAPKs and NF-κB pathways. In the mouse model of acute lung injury, histopathologic examination indicted that D(-)-Salicin suppressed edema induced by LPS.
CONCLUSIONS:
So it is suggest that D(-)-Salicin might be a potential therapeutic agent against inflammatory diseases. |
|
|
1 mg |
5 mg |
10 mg |
20 mg |
25 mg |
| 1 mM |
3.4932 mL |
17.466 mL |
34.9321 mL |
69.8641 mL |
87.3301 mL |
| 5 mM |
0.6986 mL |
3.4932 mL |
6.9864 mL |
13.9728 mL |
17.466 mL |
| 10 mM |
0.3493 mL |
1.7466 mL |
3.4932 mL |
6.9864 mL |
8.733 mL |
| 50 mM |
0.0699 mL |
0.3493 mL |
0.6986 mL |
1.3973 mL |
1.7466 mL |
| 100 mM |
0.0349 mL |
0.1747 mL |
0.3493 mL |
0.6986 mL |
0.8733 mL |
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
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