天然产物 黄酮类 Flavonoids
Quercetagetin (Synonyms: 6-Hydroxyquercetin) 纯度: 99.24%
Quercetagetin (6-Hydroxyquercetin) 是一种类黄酮。Quercetagetin 是一种中等强度和选择性的,细胞渗透性的 pim-1 激酶抑制,IC50 为 0.34 μM。具有抗炎和抗肿瘤活性。
Quercetagetin Chemical Structure
CAS No. : 90-18-6
规格 | 价格 | 是否有货 | 数量 |
---|---|---|---|
10 mM * 1 mL in DMSO | ¥3190 | In-stock | |
5 mg | ¥2900 | In-stock | |
10 mg | ¥4900 | In-stock | |
50 mg | 询价 | ||
100 mg | 询价 |
* Please select Quantity before adding items.
Quercetagetin 相关产品
•相关化合物库:
- Natural Product Library Plus
- Bioactive Compound Library Plus
- Epigenetics Compound Library
- Immunology/Inflammation Compound Library
- JAK/STAT Compound Library
- Kinase Inhibitor Library
- Natural Product Library
- Anti-Cancer Compound Library
- Phenols Library
- Traditional Chinese Medicine Monomer Library
- Flavonoids Library
- Anti-Pancreatic Cancer Compound Library
- Food-Sourced Compound Library
- Targeted Diversity Library
生物活性 |
Quercetagetin (6-Hydroxyquercetin) is a flavonoid[1]. Quercetagetin is a moderately potent and selective, cell-permeable pim-1 kinase inhibitor (IC50, 0.34 μM)[2]. Anti-inflammatory and anticancer properties. |
||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
IC50 & Target[2] |
|
||||||||||||||||
体外研究 (In Vitro) |
Quercetagetin also inhibits PIM2, PKA, and RSK2 with IC50s of 3.45, 21.2, and 2.82 µM, respectively[2]. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability Assay[2]
|
||||||||||||||||
体内研究 (In Vivo) |
Quercetagetin significantly inhibits UVB-induced skin cancer development. Topical application of 4 or 20 nmol of Quercetagetin to mouse skin reduces tumor incidence by 32.0% and 46.7%, respectively[3]. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
|
||||||||||||||||
分子量 |
318.24 |
||||||||||||||||
Formula |
C15H10O8 |
||||||||||||||||
CAS 号 |
90-18-6 |
||||||||||||||||
中文名称 |
栎草亭;六羟黄酮;六羟基黄酮 |
||||||||||||||||
运输条件 |
Room temperature in continental US; may vary elsewhere. |
||||||||||||||||
储存方式 |
|
||||||||||||||||
溶解性数据 |
In Vitro:
DMSO : 125 mg/mL (392.79 mM; Need ultrasonic) 配制储备液
*
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
|
||||||||||||||||
参考文献 |
|