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Pelargonidin3-O-[6-O-(E)-Ferulyl-2-O-{6-O-(E)-Ferulyl-β-D-glucoside}-β-D-glucoside]-5-O-(6-O-malonyl)-β-D-glucoside
Pelargonidin3-O-[6-O-(E)-Ferulyl-2-O-{6-O-(E)-Ferulyl-β-D-glucoside}-β-D-glucoside]-5-O-(6-O-malonyl)-β-D-glucoside
CAS No. 925673-36-5
Pelargonidin3-O-[6-O-(E)-Ferulyl-2-O-{6-O-(E)-Ferulyl-β-D-glucoside}-β-D-glucoside]-5-O-(6-O-malonyl)-β-D-glucoside ( 天竺葵色素-3-O-[6-O-(E)-阿魏酰基-2-O-{6-O-(E)-阿魏酰基-β-D-葡萄糖苷}-β-D-葡萄糖苷]-5-O-(6-O-丙二酰基)-β-D-葡萄糖苷 )
产品货号. M39750 CAS No. 925673-36-5
Pelargonidin3-O-[6-O-(E)-Ferulyl-2-O-{6-O-(E)-Ferulyl-β-D-glucoside}-β-D-glucoside]-5-O-(6-O-malonyl)-β-D-glucoside
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 25MG | 获取报价 | 有现货 |
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| 50MG | 获取报价 | 有现货 |
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| 100MG | 获取报价 | 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 |
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生物学信息
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产品名称Pelargonidin3-O-[6-O-(E)-Ferulyl-2-O-{6-O-(E)-Ferulyl-β-D-glucoside}-β-D-glucoside]-5-O-(6-O-malonyl)-β-D-glucoside
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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Pelargonidin3-O-[6-O-(E)-Ferulyl-2-O-{6-O-(E)-Ferulyl-β-D-glucoside}-β-D-glucoside]-5-O-(6-O-malonyl)-β-D-glucoside
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产品描述Pelargonidin3-O-[6-O-(E)-Ferulyl-2-O-{6-O-(E)-Ferulyl-β-D-glucoside}-β-D-glucoside]-5-O-(6-O-malonyl)-β-D-glucoside
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体外实验———
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体内实验———
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同义词天竺葵色素-3-O-[6-O-(E)-阿魏酰基-2-O-{6-O-(E)-阿魏酰基-β-D-葡萄糖苷}-β-D-葡萄糖苷]-5-O-(6-O-丙二酰基)-β-D-葡萄糖苷
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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 Number925673-36-5
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分子量———
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分子式———
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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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Miriplatin hydrate
Miriplatin hydrate (SM-11355 hydrate) 为有效的化疗剂,是烷化剂 (alkylator) 的一种。
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Zanthobungeanine
Zanthobungeanine has anti-inflammatory activity, it shows moderate NO production inhibitory activity with an IC50 value of 37.26 mg /L.It shows obviously inhibitoryactivity to platelet aggregation caused by platelet-activating factor (PAF). Zanthobungeanine shows the inhibitory action on the development of A549 cell only in high concentration and has no antipersonnel effect on A549 cell.
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R 892
Potent and selective bradykinin B1 receptor antagonist (ID50 values are 2.8 and > 600 nM at B1 and B2 receptors respectively). Exhibits no intrinsic agonist activity and is resistant to aminopeptidase and kininase II (ACE) cleavage. Displays hypertensive activity in vivo.
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