Ertiprotafib
CAS No. 251303-04-5
Ertiprotafib ( —— )
产品货号. M33352 CAS No. 251303-04-5
Ertiprotafib 是 PTP1B, IKK-β 的抑制剂,其 IC50 值分别是 1.6 μM,400 nM,同时也是PPARα/PPARβ 的激动剂,其 EC50 值为 ~1 μM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥1085 | 有现货 |
|
| 5MG | ¥1599 | 有现货 |
|
| 10MG | ¥2802 | 有现货 |
|
| 25MG | ¥5224 | 有现货 |
|
| 50MG | ¥7718 | 有现货 |
|
| 100MG | ¥10175 | 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Ertiprotafib
-
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Ertiprotafib 是 PTP1B, IKK-β 的抑制剂,其 IC50 值分别是 1.6 μM,400 nM,同时也是PPARα/PPARβ 的激动剂,其 EC50 值为 ~1 μM。
-
产品描述Ertiprotafib is an inhibitor of PTP1B, IkB kinase β (IKK-β), and a dual PPARα and PPARβ agonist, with an IC50 of 1.6 μM for PTP1B, 400 nM for IKK-β, an EC50 of ~1 μM for PPARα/PPARβ.
-
体外实验Ertiprotafib is a potent inhibitor of IKK-β, with an IC50 value of 400±40 nM, which is much lower than that required for the half-maximal inhibition of the p-nitrophenyl phosphatase activity of PTP1B. The reported IC50 value of Ertiprotafib against PTP1B ranges from 1.6 to 29 μM depending on the assay conditions. Ertiprotafib is at least a dual PPARα and PPARβ agonist with EC50 values for transactivation of 1 μM. Such activities readily explain the observations with suprapharmacologic doses of these.
-
体内实验As seen with treatment of ob/ob mice, both Ertiprotafib and compound 3 seem to significantly improve glucose metabolism in rats. At 25 mg/kg/day, these compounds decrease both fasting blood glucose and insulin levels compared with vehicle treated rats. Furthermore, both Ertiprotafib and compound 3 increase glucose disposal after an oral challenge. It is noteworthy that lipid levels are also reduced in treated animals. Both triglyceride and free fatty acid levels are substantially reduced in rats treated with 25 mg/kg/day of either compound. To summarize, both Ertiprotafib and compound 3 seem to be robust agents in improving glucose utilization in fa/fa rats while also decreasing lipid levels in these animals. Decreased lipid levels may be unexpected for a pure PTP1b inhibitor. It is more telling, as mentioned above, that rats treated with suprapharmacologic doses of Ertiprotafib show signs of PPAR family activation.
-
同义词——
-
通路Metabolic Enzyme/Protease
-
靶点Phosphatase
-
受体Phosphatase | IκB/IKK
-
研究领域——
-
适应症——
化学信息
-
CAS Number251303-04-5
-
分子量559.51
-
分子式C31H27BrO3S
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO 中的溶解度 : 100 mg/mL (178.73 mM; 超声助溶 )
-
SMILESCC=1C2=C(C=3C(C(Br)=C2SC1C)=CC=CC3)C4=CC(C)=C(O[C@H](CC5=CC=CC=C5)C(O)=O)C(C)=C4
-
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
-
Aloe-emodin-8-O-beta...
Aloe-emodin-8-O-beta-D-glucopyranoside 在体外对人蛋白酪氨酸磷酸酶 1B (hPTP1B) 显示出中等的生物活性。
-
IFB-088 acetate
IFB-088 acetate, a benzyl guanidine derivative, is used to treat diseases and cancers associated with the PPP1R15A pathway and associated with protein misfolding stress, Examples include tau disease, synaptic riboprotein disease, polyglutamine and polyalanine diseases, leukodystrophy, cystic fibrosis, multiple sclerosis, lysosome storage disorders, amyloidosis diseases, inflammation, metabolic disorders, cardiovascular diseases, osteoporosis, neurological trauma, and more.
-
LFHP-1c
LFHP-1c 是一种 PGAM5 抑制剂,在缺血性脑卒中中具有神经保护活性。LFHP-1c 保护血脑屏障完整性免受缺血损伤。LFHP-1c 与内皮细胞 PGAM5 结合,抑制 PGAM5 磷酸酶活性,抑制 PGAM5 与 NRF2 的相互作用。LFHP-1c 具有体外和体内保护作用。
021-51111890
购物车()
sales@molnova.cn

