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Kaempferol 3-O-beta-(6-p-coumaroyl)glucopyranosyl(1->2)-alpha-L-rhamnopyranoside
Kaempferol 3-O-beta-(6-p-coumaroyl)glucopyranosyl(1->2)-alpha-L-rhamnopyranoside
CAS No. 111957-48-3
Kaempferol 3-O-beta-(6-p-coumaroyl)glucopyranosyl(1->2)-alpha-L-rhamnopyranoside ( —— )
产品货号. M31806 CAS No. 111957-48-3
Kaempferol 3-O-beta-(6''-p-coumaroyl)glucopyranosyl(1->2)-alpha-L-rhamnopyranoside is a natural product.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 10MG | ¥2347 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称Kaempferol 3-O-beta-(6-p-coumaroyl)glucopyranosyl(1->2)-alpha-L-rhamnopyranoside
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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
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产品简述Kaempferol 3-O-beta-(6''-p-coumaroyl)glucopyranosyl(1->2)-alpha-L-rhamnopyranoside is a natural product.
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产品描述Kaempferol 3-O-beta-(6''-p-coumaroyl)glucopyranosyl(1->2)-alpha-L-rhamnopyranoside is a natural product.
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体外实验Kaempferol-3-O-(6'''-trans-p-coumaroyl-2''-glucosyl)rhamnoside (3-?O-?{2-?O-?[6-?O-?(p-?Hydroxyl-?E-?coumaroyl)?-?glucosyl]?-?(1-?2)?rhamnosyl kaempferol) is a natural from herbal medicines, with antioxidant activity.
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体内实验——
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同义词——
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通路Others
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靶点Other Targets
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受体——
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研究领域——
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适应症——
化学信息
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CAS Number111957-48-3
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分子量740.7
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分子式C36H36O17
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纯度>98% (HPLC)
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溶解度——
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SMILES——
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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Thymus factor X
Thymic factor X (TFX-Jelfa) is an aqueous extract from the thymus of a juvenile calf and is a natural stimulator of lymphocyte function.
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Antiproliferative ag...
Antiproliferative agent-36(化合物8i)是一种苯并噻唑基腙衍生的化合物,具有抗增殖活性。Antiproliferative agent-36 具有广谱抗癌活性。
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PKC ζ pseudosubstrat...
Inhibitor of protein kinase C (PKC) ζ; attached to cell permeabilisation Antennapedia domain vector peptide. Consists of amino acids 113 - 129 of PKC ζ pseudosubstrate domain linked by a disulphide bridge to the Antennapedia domain vector peptide. The Antennapedia peptide is actively taken up by intact cells, at 4 or 37°C, ensuring rapid and effective uptake of the inhibitor peptide. Once inside the cell, the disulphide bonds are subjected to reduction in the cytoplasm leading to release of the inhibitor peptide. Induces mast cell degranulation by a PKC ζ-independent pathway.
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