K-80003 (Synonyms: TX-803)
目录号: PL06152 纯度: ≥99%
CAS No. :1292821-90-9
商品编号 规格 价格 会员价 是否有货 数量
PL06152-5mg 5mg ¥2040.00 请登录
PL06152-10mg 10mg ¥3400.00 请登录
PL06152-50mg 50mg ¥10570.91 请登录
PL06152-100mg 100mg 询价 询价
PL06152-200mg 200mg 询价 询价
PL06152-10mM*1mLinDMSO 10mM*1mLinDMSO ¥2250.18 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
K-80003
中文别名
化合物 T11734
英文名称
K-80003
英文别名
K-80003;k-80003;K-80003 (TX-803);TX-803;1H-Indene-3-acetic acid, 5-fluoro-2-methyl-1-[[4-(1-methylethyl)phenyl]methylene]-, (1Z)-
Cas No.
1292821-90-9
分子式
C22H21FO2
分子量
336.40
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
K-80003 有效抑制 tRXRα 依赖性的 Akt 激活和肿瘤细胞生长。
生物活性
K-80003 is a potent inhibitor of tRXRα-dependent Akt activation and cancer cell growth.
性状
Solid
IC50 & Target[1][2]
Akt
体外研究(In Vitro)
When MCF-7 cells are cotreated with K-80003, TNFα-induced colocalization of tRXRα with p85α in the cytoplasm is inhibited, resulting in tRXRα nuclear localization. Western blotting shows that K-80003-stabilized tetrameric form of tRXRα is found exclusively in the nuclear fraction, while tRXRα monomer is distributed both in the nuclear and cytoplasmic fractions. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
K-80003 is a potent inhibitor of AKT activation by all-trans-retinoic acid. K-80003 displays enhanced efficacy in inhibiting tRXRα-dependent AKT activation and tRXRα tumor growth in animals. K-80003 has high affinity to RXRα but lacks COX inhibitory activity. 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;4°C 2 years
参考文献
[1]. Zhou H, et al. NSAID sulindac and its analog bind RXRalpha and inhibit RXRalpha-dependent AKT signaling. Cancer Cell. 2010 Jun 15;17(6):560-73.
[2]. Chen L, et al. Modulation of nongenomic activation of PI3K signalling by tetramerization of N-terminally-cleaved RXRα. Nat Commun. 2017 Jul 17;8:16066.
溶解度数据
In Vitro: DMSO : 30 mg/mL (89.18 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