| Bioactivity | Salixteroside D is a salicin derivative, that exhibits anti-inflammatory activity through inhibition of MAPK and NF-κB signaling pathways[1]. |
| Invitro | Salixteroside D (20 μM，24 h) 抑制细胞 RAW264.7 生成 NO，IC50 为 6.75 μM，对 RAW 264.7 不具备毒性[1]。Salixteroside D (5-20 μM，12 h) 在 Lipopolysaccharides (HY-D1056) 诱导的 RAW 264.7 巨噬细胞中抑制炎症介质 IL-1β，IL-6，iNOS 和 COX-2 的表达[1]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> Salixteroside D 相关抗体: Western Blot Analysis[1] Cell Line: |
| Formula | C22H26O11 |
| Molar Mass | 466.44 |
| Transport | Room temperature in continental US; may vary elsewhere. |
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
| Reference | [1]. Wu PQ, et al., Anti-Inflammatory Salicin Derivatives from the Barks of Salix tetrasperma. J Agric Food Chem. 2024 Apr 11. |