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- 文献和实验
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1454585-06-8
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1268.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥480.0 |
| 规格: | 5 mg | 产品价格: | ¥1200.0 |
| 规格: | 10 mg | 产品价格: | ¥1900.0 |
| 规格: | 25 mg | 产品价格: | ¥3800.0 |
| 规格: | 50 mg | 产品价格: | ¥5447.0 |
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SR-3029
CAS No. : 1454585-06-8
MCE 国际站:SR-3029
产品活性:SR-3029 是一种有效的,ATP 竞争性的 CK1δ 和 CK1ε 的抑制剂,IC50 值分别为 44 nM 和 260 nM,Ki 均为 97 nM。
研究领域:Cell Cycle/DNA Damage | Stem Cell/Wnt
作用靶点:Casein Kinase
In Vitro: SR-3029 is a potent CK1δ/CK1ε inhibitor, with IC50s of 44 nM and 260 nM, respectively. SR-3029 is ATP competitive, with Kis of 97 nM for CK1δ/CK1ε. SR-3029 also blocks CDK6/cyclin D3, CDK6/cyclin D1, CDK4/cyclin D3, CDK4/cyclin D1 and FLT3, with IC50s of 427, 428, 368, 576, and 3000 nM, respectively. SR-3029 shows inhibitory effects on A375 cells, with an EC50 of 86 nM. CK1δ is a necessary and sufficient driver of Wnt/β-catenin signaling in human breast cancer. SR-3029 shows less potent activities against MCF7 and T47D breast cancer cells and the MCF10A cell line, which express low amounts of CK1δ.
In Vivo: SR-3029 (20 mg/kg daily i.p.) exibits anti-tumor effects in rthotopic MDA-MB-231, MDA-MB-468 (TNBC), SKBR3 and BT474 (HER2+) tumor xenografts with no overt toxicity in mice. SR-3029 (20 mg/kg daily i.p.) also effectively inhibits the growth of tumor in primary patient-derived xenograft (PDX) models. In addition, SR-3029 (20 mg/kg, i.p.) strongly reduces the expression of nuclear β-catenin in tumors of mice.
相关产品:Bioactive Compound Library Plus | Cell Cycle/DNA Damage Compound Library | Kinase Inhibitor Library | Stem Cell Signaling Compound Library | Wnt/Hedgehog/Notch Compound Library | Anti-Cancer Compound Library | Anti-Aging Compound Library | Anti-Breast Cancer Compound Library | Targeted Diversity Library | Cancer Stem Cells Compound Library | Heterocyclic Compound Library | Membrane Protein-targeted Compound Library | Highly Selective Inhibitors Library | Serine/Threonine Kinase Inhibitor Library | LY294002 | Silmitasertib | IWP-2 | Emodin | Ellagic acid | D4476 | Umbralisib | PF-670462 dihydrochloride | TBB | TMX-4116 | Casein Kinase inhibitor A51 | DMAT | PF-4800567 | (E/Z)-GO289 | SSTC3 | IC261 | TAK-715 | FPFT-2216 | CKI-7 free base | SGC-CK2-1 | CK1-IN-1 | TTP 22 | BTX161 | AMG-548 dihydrochloride | BioE-1115 | Hematein | TA-01 | MRT00033659 | CK2/ERK8-IN-1
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文献和实验结构。(1)配位数为12的立方面心最密堆积(A 1 型,即重复ABC三层的堆积),空间利用率为74.06%,如Cu副族、Pb、Al、Tl、Ni副族、Sr等。(2)配位数为12的六方最密堆积,空间利用率为74.06%,如钪副族、Be、Mg、Hf、Tc、Re、CO等。(3)配位数为8(或14)的立方体心密堆积,空间利用率为68.02%,如碱金属、V副族、Cr副族、Ti、Zr、Zn、Cd、Ca、Sr、Ba等。(4)配位数为4的金刚石型四面体堆积(A 4 型),空间利用率为34.01%,如Si
) Sr 38 87.62 硫(sulfur) S 16 32.06 钽(tantalum) Ta 73 180.94
、Fe、Zn、Sr、Mn等人体必须的矿物质元素 ,因此椒目仁油可成为稀有的功能性食用油及新型的中药原料。超临界流体萃取具有无毒、无污染、快速廉价、操作简便等优点,并可通过对提取温度和压力的调节来改变其溶解性能,达到将不同成分分离的效果l2]。本实验就椒目仁油的超临界CO2流体萃取工艺进行了研究。 1 材料与仪器:椒目购自陕西盛华药业有限公司,为陕西韩城产大红袍花椒晒干,除去果皮、果柄及杂质;CO2(西安兴华BOC气体有限公司)。FY221-50-06型超临界萃取装置(南通市飞宇石油科技
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