
YTX-465
CAS No. 2225824-53-1
YTX-465 ( —— )
产品货号. M28861 CAS No. 2225824-53-1
YTX-465 是硬脂酰辅酶 A 去饱和酶 (IC50s = 39 nM) 和 Ole1 (IC50s = 30.4 μM) 的抑制剂。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥5038 | 有现货 |
![]() ![]() |
10MG | ¥7962 | 有现货 |
![]() ![]() |
25MG | ¥11826 | 有现货 |
![]() ![]() |
50MG | ¥15957 | 有现货 |
![]() ![]() |
100MG | ¥21465 | 有现货 |
![]() ![]() |
200MG | 获取报价 | 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YTX-465
-
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YTX-465 是硬脂酰辅酶 A 去饱和酶 (IC50s = 39 nM) 和 Ole1 (IC50s = 30.4 μM) 的抑制剂。
-
产品描述YTX-465 is an inhibitor of both stearoyl-CoA desaturase(IC50s = 39 nM) and Ole1 (IC50s = 30.4 μM).(In Vitro):YTX-465 rescued growth to a similar magnitude but was >100-fold more potent than YTX-528(EC50 = 0.013 μM). Kinetic growth studies demonstrated that the most effective concentration of YTX-465 (0.050 μM) restored growth rates to that of approximately 40% of the wild-type strain treated with the same concentration of YTX-465. In wild-type yeast, YTX-465 strongly reduced fatty desaturation in a concentration-dependent manner, with a 50% reduction in desaturation at 0.03 μM YTX-465.
-
体外实验YTX-465 (1-10000 nM) has an EC50 value of 0.013 μM for α-synuclein (α-syn) toxicity rescue.YTX-465 (0.05 μM; 0-2 days) rescue the growth of α-Syn-expressing yeast.YTX-465 (0, 10, 40, 160, 640, 2500 nM; 4h) increases the level of Ole1 protein in wild-type yeast expressing OLE1 in a concentration-dependent manner, that indicate YTX-465 induce a negative feedback loop.YTX-465 (0, 0.03, 0.09, 0.27, 0.81 μM; 6 hours) reduces fatty desaturation in a concentration-dependent manner in wild-type yeast, with a 50% reduction in desaturation at 0.03 μM.YTX-465 (0.25 μM; 8 hours) decreases the desaturation index (DI) for all major classes of membrane phospholipids in wild-type yeast.
-
体内实验——
-
同义词——
-
通路Metabolic Enzyme/Protease
-
靶点SCD
-
受体EML4-ALK
-
研究领域——
-
适应症——
化学信息
-
CAS Number2225824-53-1
-
分子量458.51
-
分子式C25H26N6O3
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 100 mg/mL (218.10 mM)
-
SMILESCc1nn(C)c2c1ccc(-c1noc(C(CC3)CCN3C(CNC(c3ccccc3)=O)=O)n1)c2
-
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
1.Iikubo K, et al. Synthesis and structure-activity relationships of pyrazine-2-carboxamide derivatives as novel echinoderm microtubule-associated protein-like 4 (EML4)-anaplastic lymphoma kinase (ALK) inhibitors. Bioorg Med Chem. 2019 Apr 15;27(8):1683-1692.