Axinelline A
Axinelline A is a potent COX inhibitor with IC50s of 2.22 μM and 8.89 μM against COX-2 and COX-1, respectively. Axinelline A shows anti-inflammatory activity.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 1593741-99-1
- 分子式: C12H15NO6
- 分子量:269.25
-
保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
|
COX-2 2.22 μM (IC50) |
COX-1 8.89 μM (IC50) |
Axinelline A (2-30 μM; 24 h) inhibits Lipopolysaccharide (LPS; HY-D1056)-induced expression of pro-inflammatory factors (NO, TNF-α, IL-6, IL-1β, and PGE2) in RAW264.7 cells[1].
Axinelline A (2-30 μM; 24 h) inhibits LPS-induced NF-κB signaling pathway in RAW264.7 cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:RAW264.7 cells
-
Concentration:2, 10 and 30 μM
-
Incubation Time:24 h
-
Result:Diminished LPS-induced expression of nitric oxide synthase (iNOS) and COX-2 protein levels. The phosphorylation level of NF-κB increased after 30 min of LPS treatment, but pretreatment with test compound reduced the level of phosphorylation in a dose-dependent manner. The phosphorylation of IKK and IκBα was inhibited in a dose-dependent manner.
化学情報
-
CAS 番号 1593741-99-1
-
分子量 269.25
-
分子式 C12H15NO6
-
SMILES
CCOC([C@H](CO)NC(C1=C(C(O)=CC=C1)O)=O)=O
-
Structure Classification
-
Initial Source
Streptomyces axinellae
-
輸送条件
Room temperature in continental US; may vary elsewhere.
-
保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)