Kushenol A
CAS No. 99217-63-7
Kushenol A ( —— )
产品货号. M31172 CAS No. 99217-63-7
Kushenol A is a kind of Adenosine 3', 5'-cyclic monophosphate(cAMP)phosphodiesterase inhibitiors, it shows selective alpha-glucosidase inhibitory activity.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥5681 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Kushenol A
-
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Kushenol A is a kind of Adenosine 3', 5'-cyclic monophosphate(cAMP)phosphodiesterase inhibitiors, it shows selective alpha-glucosidase inhibitory activity.
-
产品描述Kushenol A is a kind of Adenosine 3', 5'-cyclic monophosphate(cAMP)phosphodiesterase inhibitiors, it shows selective alpha-glucosidase inhibitory activity. Kushenol A and kushenol C exhibit inhibitory activity against Sodium-dependent glucose cotransporter 2(SGLT2).
-
体外实验Kushenol A (25?μM) exhibits a highly potent inhibitory activity on ABTS+?radical scavenging with an IC50 value of 9.7?±?0.1?μM, and exhibits inhibits scavenging activity as a percentage 93.7% at 25?μM.Kushenol A (0-60 μg/ml; 24 hours) shows considerable cytotoxic effects against NSCLC cells, exhibits IC50 values of 5.3 μg/ml and 20.5 μg/ml for A549 and NCI‐H226 cells, respectively. It shows an IC50 value of 57.2 μg/ml for BEAS-2B cells.Cell Viability Assay Cell Line:NSCLC cell lines, A549 and NCI-H226Normal human lung epithelial: BEAS-2B Concentration:0-60 μg/ml Incubation Time:24 hoursResult:Exhibited considerable cytotoxic effects against NSCLC cells.
-
体内实验——
-
同义词——
-
通路Others
-
靶点Other Targets
-
受体——
-
研究领域——
-
适应症——
化学信息
-
CAS Number99217-63-7
-
分子量408.5
-
分子式C25H28O5
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 100 mg/mL (244.80 mM)
-
SMILES——
-
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
产品手册
关联产品
-
MOPS
MOPS 在生物学中通常用作缓冲剂。 MOPS 缓冲液可以维持哺乳动物细胞培养基的 pH 值。
-
Isoorientin 7-O-gluc...
Lutonarin 是一种从青稞叶中分离得到的抗氧化剂。Lutonarin 与 Saponarin联合使用时抑制所有脂质的丙二醛形成。
-
6-O-Acetyldaidzin
6"-O-Acetyldaidzin 是大豆中的一个异黄酮糖苷。在大鼠肝微粒体中,6"-O-Acetyldaidzin 显著抑制脂质过氧化反应的 IC50 值为 8.2 μM。
021-51111890
购物车()
sales@molnova.cn

