6-Methoxyluteolin
CAS No. 520-11-6
6-Methoxyluteolin ( —— )
产品货号. M22556 CAS No. 520-11-6
6-甲氧基木犀草素具有抗氧化活性,它是通过下调 FcεRI α 链而有效抑制组胺释放和钙内流的抑制剂。使用人类嗜碱性 KU812F 细胞,我们评估了从菊花中分离的 6-甲氧基木犀草素的抑制作用, FcαμRI 介导的过敏反应。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1568 | 有现货 |
|
| 10MG | ¥2518 | 有现货 |
|
| 25MG | ¥4046 | 有现货 |
|
| 50MG | ¥5720 | 有现货 |
|
| 100MG | ¥7452 | 有现货 |
|
| 200MG | ¥9810 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥1682 | 有现货 |
|
生物学信息
-
产品名称6-Methoxyluteolin
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述6-甲氧基木犀草素具有抗氧化活性,它是通过下调 FcεRI α 链而有效抑制组胺释放和钙内流的抑制剂。使用人类嗜碱性 KU812F 细胞,我们评估了从菊花中分离的 6-甲氧基木犀草素的抑制作用, FcαμRI 介导的过敏反应。
-
产品描述6-Methoxyluteolin has antioxidant activity, it is a potent inhibitor of histamine release and calcium influx via down-regulation of the FcεRI α chain.Using the human basophilic KU812F cells, we assessed the inhibitory effects of 6-Methoxyluteolin, isolated from Chrysanthemum zawadskii, in the FcαμRI-mediated allergic reaction. We determined that 6-Methoxyluteolin inhibited anti-FcαμRI α± chain antibody (CRA-1)-induced histamine release, as well as elevation of intracellular calcium concentration [Ca2+]i in a dose-dependent manner. Moreover, the inhibitory effects of 6-Methoxyluteolin on the cell surface expression and the mRNA level of the FcαμRI α± chain were determined by flow cytometric analysis and reverse transcription-polymerase chain reaction (RTPCR), respectively.
-
体外实验Pretreatment with Nepetin dose-dependently inhibited IL-6, IL-8 and MCP-1 secretion with IC50 values of 4.43, 3.42 and 4.17 μM, respectively.Nepetin (2.5-10 μM; 25 hours; ARPE-19 cells) treatment suppresses IL-1β-induced cytokine (IL-6, IL-8 and MCP-1) expression at mRNA level in ARPE-19 cells.Nepetin (2.5-10 μM; 1.5 hours; ARPE-19 cells) treatment dose-dependently inhibits phosphorylation of IKKα/β and IκBα, and nuclear translocation of p65. Nepetin decreases the level of phosphorylated ERK1/2, JNK and p38 MAPK in activated ARPE-19 cells. RT-PC RCell Line:ARPE-19 cells Concentration:2.5 μM, 5 μM, 10 μM Incubation Time:25 hours Result:Suppressed the mRNA expression of IL-6, IL-8 and MCP-1 in ARPE-19 cells. Western Blot Analysis Cell Line:ARPE-19 cells Concentration:2.5 μM, 5 μM, 10 μM Incubation Time:1.5 hours Result:Dose-dependently inhibited phosphorylation of IKKα/β and IκBα, and nuclear translocation of p65. Decreased the level of phosphorylated ERK1/2, JNK and p38 MAPK in activated ARPE-19 cells.
-
体内实验——
-
同义词——
-
通路GPCR/G Protein
-
靶点Calcium Channel
-
受体Calcium Channel|Histamine Receptor
-
研究领域——
-
适应症——
化学信息
-
CAS Number520-11-6
-
分子量316.26
-
分子式C16H12O7
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 125 mg/mL (395.24 mM)
-
SMILESCOc1c(O)cc2oc(cc(=O)c2c1O)-c1ccc(O)c(O)c1
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.6-Methoxyluteolin from Chrysanthemum zawadskii var. latilobum suppresses histamine release and calcium influx via down-regulation of FcαμRI α± chain expression.J Microbiol Biotechnol. 2012 May;22(5):622-7.
产品手册
关联产品
-
Lifarizine
Lifarizine (RS-87476), a calcium-sodium channel antagonist, shows neuroprotective activity in a simplified rat survival model of double vessel occlusion.
-
GV-58
GV-58 是一种有效的选择性 N 型和 P/Q 型 Ca2+ 通道激动剂,EC50 分别为 7.2 和 8.8 uM。
-
Atagabalin HCl
Atagabalin HCl is a novel voltage-dependent calcium channel (VDCC) α2δ subunit (1 and 2) ligand that affects slow-wave sleep and can be used to treat insomnia.
021-51111890
购物车()
sales@molnova.cn

