Cajanin
CAS No. 32884-36-9
Cajanin ( —— )
产品货号. M30929 CAS No. 32884-36-9
Cajanin has potential hypolipidemic effects,possibly via up-regulating the ABCA1 protein expression,subsequently resulting in increased macrophage cholesterol efflux and RCT, it can significantly improve basal glucose uptake in HepG2 cells, its improving effect is concentration dependent, it exhibits effects stronger than that of rosiglitazone, which has been used as an antidiabetic drug.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥14013 | 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Cajanin
-
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Cajanin has potential hypolipidemic effects,possibly via up-regulating the ABCA1 protein expression,subsequently resulting in increased macrophage cholesterol efflux and RCT, it can significantly improve basal glucose uptake in HepG2 cells, its improving effect is concentration dependent, it exhibits effects stronger than that of rosiglitazone, which has been used as an antidiabetic drug.
-
产品描述Cajanin has potential hypolipidemic effects,possibly via up-regulating the ABCA1 protein expression,subsequently resulting in increased macrophage cholesterol efflux and RCT, it can significantly improve basal glucose uptake in HepG2 cells, its improving effect is concentration dependent, it exhibits effects stronger than that of rosiglitazone, which has been used as an antidiabetic drug.
-
体外实验Cajanin shows strong mitogenic as well as differentiation-promoting effects on osteoblasts.Cajanin induces the phosphorylation of both Erk1/2 and Akt.
-
体内实验Cajanin (10 mg/kg, p.o.; daily for 30 consecutive days) increases the BMD levelsin all anatomical regions of the skeleton studied in Sprague Dawley rats.
-
同义词——
-
通路Others
-
靶点Other Targets
-
受体——
-
研究领域——
-
适应症——
化学信息
-
CAS Number32884-36-9
-
分子量300.3
-
分子式C16H12O6
-
纯度>98% (HPLC)
-
溶解度——
-
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
-
NRX-1933
NRX-1933 是一种分子胶,可增强致癌转录因子 β-Catenin 与其同源 E3 连接酶 SCFβ-TrCP 之间的相互作用。
-
GTPγS tetralithium
GTPγS (tetralithium) 是一种 G 蛋白激活剂,可保护蛋白质免遭蛋白水解降解,以酪氨酸激酶依赖性方式刺激 GLUT4 易位,刺激磷脂酶并诱导肌动蛋白聚合。GTPγS (tetralithium) 和 G 蛋白 α 联合可以用来研究激酶活力。GTPγS (tetralithium) 可以作为裂解缓冲液的组成成分。
-
NSC756093
NSC756093 可能抑制 GBP1:PIM1 相互作用。 NSC756093 可用于卵巢癌研究。
021-51111890
购物车()
sales@molnova.cn

