PROTAC ERRα Degrader-3
目录号: PL03814 纯度: ≥98%
CAS No. :2306388-65-6
商品编号 规格 价格 会员价 是否有货 数量
PL03814-5mg 5mg ¥3709.09 请登录
PL03814-10mg 10mg ¥5934.55 请登录
PL03814-25mg 25mg ¥11745.45 请登录
PL03814-50mg 50mg ¥17927.27 请登录
PL03814-100mg 100mg 询价 询价
PL03814-200mg 200mg 询价 询价
PL03814-10mM*1mLinDMSO 10mM*1mLinDMSO ¥4080.00 请登录
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
中文名称
PROTAC ERRα Degrader-3
英文名称
PROTAC ERRα Degrader-3
英文别名
PROTAC ERRα Degrader-3;2306388-65-6;PROTAC ERRalphaDegrader-3;CHEMBL4570799;A Degrader-3;(2S,4R)-1-[(2S)-2-{5-[(2E)-3-(4-{[2,4-bis(trifluoromethyl)phenyl]methoxy}-3-methoxyphenyl)-2-cyanoprop-2-enamido]pentanamido}-3,3-dimethylbutanoyl]-4-hydroxy-N-{[4-(4-methyl-1,3-thiazol-5-yl)phenyl]methyl}pyrrolidine-2-carboxamide;EN300-44822897;CS-0181524;AKOS040757542;PROTAC ERRalpha Degrader-3;Z5713235440;PROTAC ERR;HY-139185;BDBM50501976;MS-31788;PROTAC ERR?? Degrader-3
Cas No.
2306388-65-6
分子式
C47H50F6N6O7S
分子量
956.99
包装储存
Powder -20°C 3 years;In solvent -80°C 6 months
产品详情
PROTAC ERRα Degrader-3 是一种基于 von Hippel-Lindau 配体的强效选择性 ERRα 降解剂。PROTAC ERRα Degrader-3 能够在 30 nM 的浓度下将 ERRα 蛋白特异性降解 >80%。PROTAC ERRα Degrader-3 对 ERRβ
生物活性
PROTAC ERRα Degrader-3 is a potent and selective ERRα degrader based on von Hippel-Lindau ligand. PROTAC ERRα Degrader-3 is capable of specifically degrading ERRα protein by >80% at a concentration of 30 nM. PROTAC ERRα Degrader-3 is inactive against ERRβ and ERRγ proteins.
性状
Solid
IC50 & Target[1][2]
ERRα VHL
体外研究(In Vitro)
PROTAC ERRα Degrader-3 (compound 6c; 0.3 nM-10 μM; 4 hours) dose-dependently induces ERRα degradation with an efficacious dose as low as 3.0 nM at 4.0 h. PROTAC ERRα Degrader-3 potently decreases protein levels of ERRα downstream target genes, e.g., ATP5B, medium-chain acyl CoA dehydrogenase (MCAD), and pyruvate dehydrogenase kinase 4 (PDK4) in the MDA-MB-231 cells after a 24 h treatment.
PROTAC ERRα Degrader-3 exhibits an IC50 value of 12.67 nM to block the protein-protein interaction of ERRα with PGC-1α peptide and induces approximately 96% protein degradation at 100 nM (D100 nM) after 4.0 h treatment. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;In solvent -80°C 6 months
参考文献
[1]. Lijie Peng, et al. Identification of New Small-Molecule Inducers of Estrogen-related Receptor α (ERRα) Degradation. ACS Med Chem Lett. 2019 Apr 12;10(5):767-772.
溶解度数据
In Vitro: DMSO : 80 mg/mL (83.60 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2