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- 保存条件:
4°C, protect from light
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1245319-54-3
- 规格:
10 mM * 1 mL/2 mg/5 mg/10 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥3654.0 |
|---|---|---|---|
| 规格: | 2 mg | 产品价格: | ¥2480.0 |
| 规格: | 5 mg | 产品价格: | ¥3720.0 |
| 规格: | 10 mg | 产品价格: | ¥6696.0 |
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PI4KIII beta inhibitor 3
CAS No. : 1245319-54-3
MCE 国际站:PI4KIII beta inhibitor 3
产品活性:PI4KIII beta inhibitor 3 是一种新型高效的 ΡΙ4ΚΙΙΙβ 抑制剂,IC50 为 5.7 nM。
研究领域:PI3K/Akt/mTOR
作用靶点:PI4K
In Vitro: PI4KIII beta inhibitor 3 is a PI4KIII inhibitor extracted from patent WO/2013034738 A1, the compound of formula 3, has an IC50 of 5.7 nM. PI4KIII beta inhibitor 3 exerts significant immunosuppressive activity, with IC50 value of 3 nM in the mixed lymphocyte reaction (MLR) assay. PI4KIII beta inhibitor 3 inhibits IL2 and IFNy secretion with IC50 values of less than InM in each case. Thus, PI4KIII beta inhibitor 3 is shown to be as effective at inhibiting IL2 and IFNy secretion as conventional immunosuppressants such as cyclosporine A. IC50 on IFNy and IL-2 release of Cyclosporine A are 2nM and less than 1 nM respectively.
In Vivo: PI4KIII beta inhibitor 3 (40 mg/kg per day, n=12) is able to delay the onset of arthritic symptoms and also to decrease symptom severity in a preventive model of arthritis compared to a vehicle control (MC 1%, n=12). PI4KIII beta inhibitor 3 reduces the anti-CII IgG titre and histological scores in the collagen-induced arthritis mouse model. Oral administration of PI4KIII beta inhibitor 3 results in prolonged graft survival in 3 out of 6 grafts in each group at day 30. Several grafts continued beating after withdrawal of the treatment (up to 60 days), indicating the induction of a certain type of graft tolerance. To evaluate the operational tolerance phenotype, animals with functional graft at day 60 are challenged with a second graft from the same donor strain or from a third party. No treatment is applied. The second grafts from the third party are rejected at day 8 (n=2) whereas second grafts from the same donor strain are functional for more than 90 days (n=2).
相关产品:Bioactive Compound Library Plus | Kinase Inhibitor Library | PI3K/Akt/mTOR Compound Library | Anti-Cancer Compound Library | Anti-Aging Compound Library | Oxygen Sensing Compound Library | Glycolysis Compound Library | Cytoskeleton Compound Library | Anti-Pancreatic Cancer Compound Library | Anti-Cancer Metabolism Compound Library | Anti-Obesity Compound Library | Glucose Metabolism Compound Library | Targeted Diversity Library | Cancer Stem Cells Compound Library | Membrane Protein-targeted Compound Library | Highly Selective Inhibitors Library | PIK-93 | BF738735 | PI-273 | PI4KIIIbeta-IN-10 | T-00127_HEV1 | BQR-695 | PI4KIIIbeta-IN-9 | GSK-A1 | MMV390048 | KDU691 | UCB9608 | BI-1622 | GSK-F1 | KDU731 | UCT943 | AL-9 | CHMFL-PI4K-127 | EDI048 | MI 14 | MIPS-21335 | PI4K-IN-1 | PI4KIIIbeta-IN-11
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文献和实验【求助】如何证明GSK-3beta的抑制是由Wnt通路引起的?
magichunter 我现在能够证明GSK-3beta的活性受到了抑制,同时也证明了b-catenin在核内和胞浆内的表达都升高了,同时胞浆内的磷酸化b-catenin含量降低(Wnt通路被激活了吗)。另外Akt的磷酸化增高(应该是PI3K/Akt通路被激活了)。因为Wnt和PI3K/Akt两条通路都可以抑制GSK的活性。 请问能否判断GSK的抑制是由Wnt通路的激活引起的,还是有PI3K/Akt的激活引起的?还是两条通路都激活了? (暂时我还不能进行
真爱满行囊 我最近在体外细胞做的关于gsk3-beta功能问题,发现药物处理以后,gsk-3-beta的总表达量下调,如果是这样的话 1、我是否能够得出gsk-3-beta的活性下调的结论? 2、是否还有必要做非活性形式的表达量?我的理解是,基础状态下,gsk-3beta维持的是低活性状态,如果总量都下调了,那应该能够得出活性降低的结论了吧? 3、另外,在这种情况下我是否有必要去做gsk-3-beta的216位点的活性形式的表达
fanjingol 如题所示!小弟我做的是兔的脊髓缺血再灌的实验!查阅了相关文献是:鼠中使用的量1.0 mg/kg in25% DMSO in PBS!请问有高人告诉我在兔中的量应该是多少啊? 万分感谢! dai88 学习了, 请问你用什么抑制剂呀,那么大的用量不是很贵吗? yhwangcams 没做过,但可以用关键词PI3K inhibitor, rabbit model
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