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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
4°C, protect from light
- 英文名:
Tyrphostin AG 494
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
133550-35-3
- 规格:
10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥286.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥260.0 |
| 规格: | 10 mg | 产品价格: | ¥450.0 |
| 规格: | 25 mg | 产品价格: | ¥900.0 |
| 规格: | 50 mg | 产品价格: | ¥1450.0 |
| 规格: | 100 mg | 产品价格: | ¥2500.0 |
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AG-494
CAS No. : 133550-35-3
MCE 国际站:AG-494
产品活性:AG-494 (Tyrphostin AG 494) 是一种高效、选择性的 EGFR 酪氨酸激酶抑制剂 (IC50=0.7 μM)。AG-494 抑制EGFR、ErbB2、HER1-2 和 PDGF-R 的自磷酸化,IC50 为 1.1,39,45 和 6 μM。AG-494 阻断 Cdk2 的激活并抑制 EGF 依赖的 DNA 合成。
研究领域:JAK/STAT Signaling | Protein Tyrosine Kinase/RTK | Cell Cycle/DNA Damage
In Vitro: In DHER-14 cells, AG 494 inhibits Cdk2 activation and EGF-dependent DNA synthesis.
AG-494 significantly prevents NF-kB activation in silica-stimulated cells, and also reduces NF-kB activation in H2O2-treated cells.
AG-494 (3-9 μM; 5-7 days) inhibits BMP9-induced ALP activity in a dose-dependent manner.
相关产品:Covalent Screening Library Plus | Bioactive Compound Library Plus | Cell Cycle/DNA Damage Compound Library | Immunology/Inflammation Compound Library | JAK/STAT Compound Library | Kinase Inhibitor Library | Protein Tyrosine Kinase Compound Library | Anti-Cancer Compound Library | Anti-Aging Compound Library | Covalent Screening Library | Differentiation Inducing Compound Library | Anti-Hepatitis C Virus Compound Library | Anti-Breast Cancer Compound Library | Anti-Lung Cancer Compound Library | Anti-Pancreatic Cancer Compound Library | Anti-Blood Cancer Compound Library | Anti-Obesity Compound Library | Angiogenesis-Related Compound Library | Anti-Liver Cancer Compound Library | Anti-Colorectal Cancer Compound Library | Anti-Prostate Cancer Compound Library | Cancer Stem Cells Compound Library | Membrane Protein-targeted Compound Library | Membrane Receptor-targeted Compound Library | Cysteine Targeted Covalent Library | Highly Selective Inhibitors Library | Cytokine Inhibitors Library | Serine/Threonine Kinase Inhibitor Library | Osimertinib | Palbociclib | Trastuzumab | Gefitinib | Cetuximab | Erlotinib | Abemaciclib | Afatinib | Ro-3306 | Lapatinib | Ribociclib | AG490 | Dinaciclib | Trastuzumab deruxtecan | Genistein | Neratinib | GSK3326595 | Tucatinib | THZ1 | Flavopiridol | Trastuzumab emtansine | SR-4835 | (R)-Roscovitine | THZ531 | AZD4573 | SY-5609 | AG-1478
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文献和实验一、原理HCG是放射性同位素标记技术与抗原抗体免疫反应相结合的超微量分析法,是用放射性核素(如125I/3H)标记的极微量的示踪抗原*(Ag*)/抗体*(Ab*)与待测抗原Ag/抗体Ag)一起来竞争结合有限的特异性抗体(Ab)/抗原(Ag),故称饱和分析或竞争抑制法。其反应过程为:Ag*•Ab量固定,Ag*+Ag>Ab可结合的数目(抗原过量),Ag*与Ag竞争结合Ab,直到反应达到平衡,形成的AD*•Ab量随着Ag量改变:Ag量大,与Ab结合的机会多,Ag*•.Ab少,反之,则形成的Ag*•.
文献速递|Cell 封面:应激颗粒异常互作介导 CMT2 周围神经病变的共同机制
of oligodendrocyte maturation. Neuron 109, 3104-3118 e3106 (2021). Saxena, S. and P. Caroni, Selective neuronal vulnerability in neurodegenerative diseases: from stressor thresholds to degeneration. Neuron, 2011. 71(1): p. 35-48. Goldman, S.M., Environmental
相关专题 抗原实验技术及研究进展 (一)原理 当抗原 遇到相应的抗体便形成抗原抗体复合物(Ag+Ab ↔Ag -Ab),当用放射性同位素标记抗原再与相应的抗体结合便形成标记抗原和抗体复合物。即: *Ag+Ab↔ *Ag-Ab。 当标记抗原 和未标记抗原一起加入相应的抗体时则两种抗原产生相互的竞争,而生成有标记抗原和抗体复合物以及非标记抗原和抗体复合物。 生成标记抗原 抗体复合
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