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Submit ReviewAG 1478 hydrochloride
说明： Highly potent EGFR-kinase inhibitor
别名： Tyrphostin AG 1478
化学名： N-(3-Chlorophenyl)-6,7-dimethoxy-4-quinazolinanine hydrochloride
纯度： ≥98% (HPLC)
生物活性 for AG 1478 hydrochloride
AG 1478 hydrochloride is a potent and selective inhibitor of epidermal growth factor receptor kinase (IC50 values 3 nM for EGFR and > 100 μM for ErbB2 and PDGFR). Inhibits proliferation of NCI-H2170 NSCLC cells in vitro (IC50 = 1 μM).
许可信息
Sold with the permission of AstraZeneca UK Ltd.
技术数据 for AG 1478 hydrochloride
| 分子量 | 352.22 |
| 公式 | C16H14ClN3O2.HCl |
| 储存 | Desiccate at -20°C |
| 纯度 | ≥98% (HPLC) |
| CAS Number | 170449-18-0 |
| PubChem ID | 3035187 |
| InChI Key | WDJDYIUSDDVWKB-UHFFFAOYSA-N |
| Smiles | ClC1=CC(NC2=NC=NC3=C2C=C(OC)C(OC)=C3)=CC=C1.Cl |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶解性数据 for AG 1478 hydrochloride
| 溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
|---|---|---|---|
| 溶解性 | |||
| DMSO | 3.52 | 10 温和加热 |
制备储备液 for AG 1478 hydrochloride
以下数据基于产品分子量 352.22。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
| 浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.1 mM | 28.39 mL | 141.96 mL | 283.91 mL |
| 0.5 mM | 5.68 mL | 28.39 mL | 56.78 mL |
| 1 mM | 2.84 mL | 14.2 mL | 28.39 mL |
| 5 mM | 0.57 mL | 2.84 mL | 5.68 mL |
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产品说明书 for AG 1478 hydrochloride
参考文献 for AG 1478 hydrochloride
参考文献是支持产品生物活性的出版物。
Eguchi et al (1998) Calcium-dependent epidermal growth factor receptor transactivation mediates the angiotensin II-induced mitogen-activated protein kinase activation in vascular smooth muscle cells. J.Biol.Chem. 273 8890 PMID: 9535870
Han et al (1996) Tyrphostin AG 1478 preferentially inhibits human glioma cells expressing truncated rather than wild-type epidermal growth factor receptors. Cancer Res. 56 3859 PMID: 8752145
Puri and Salgia (2008) Synergism of EGFR and c-Met pathways, cross-talk and inhibition, in non-small cell lung cancer. J.Carcinog. 7 9 PMID: 19240370
Levitzki and Gazit (1995) Tyrosine kinase inhibition: an approach to drug development. Science 267 1782 PMID: 7892601
If you know of a relevant reference for AG 1478 hydrochloride, please let us know.
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20 篇 AG 1478 hydrochloride 的引用文献
引用文献是使用了 Tocris 产品的出版物。 AG 1478 hydrochloride 的部分引用包括：
Ledonne et al (2015) Neuregulin 1 signalling modulates mGluR1 function in mesencephalic dopaminergic neurons. Mol Psychiatry 20 959 PMID: 25266126
O'Keeffe et al (2009) DA-induced proliferation of adult neural precursor cells in the mammalian subventricular zone is mediated through EGF. Proc Natl Acad Sci U S A 106 8754 PMID: 19433789
Gillman et al (2017) Epidermal Growth Factor Receptor Signaling Enhances the Proinflammatory Effects of Staphylococcus aureus Gamma-Toxin on the Mucosa. Toxins (Basel) 9 PMID: 28657583
Ayoub et al (2013) Profiling epidermal growth factor receptor and heregulin receptor 3 heteromerization using receptor tyrosine kinase heteromer investigation technology. PLoS One 8 e64672 PMID: 23700486
Akhtar et al (2013) Activation of ErbB2 and Downstream Signalling via Rho Kinases and ERK1/2 Contributes to Diabetes-Induced Vascular Dysfunction. PLoS One 8 e67813 PMID: 23826343
Bayliss and Evans (2013) Characterisation of AmphiAmR11, an amphioxus (Branchiostoma floridae) D2-DA-like G protein-coupled receptor. PLoS One 8 e80833 PMID: 24265838
Voon et al (2013) EMT-induced stemness and tumorigenicity are fueled by the EGFR/Ras pathway. PLoS One 8 e70427 PMID: 23950932
Zhu (2017) Increased NRG1-ErbB4 signaling in human symptomatic epilepsy Sci Rep 7 141 PMID: 28273943
Leonetti et al (2017) Tissue-type plasminogen activator exerts EGF-like chemokinetic effects on oligodendrocytes in white matter (re)myelination. Mol Neurodegener 12 20 PMID: 28231842
Hosseini et al (2018) FGF2-dependent mesenchyme and laminin-111 are niche factors in salivary gland organoids. J Cell Sci 131 PMID: 29361536
Koeppen (2018) Hypoxia-inducible factor 2-alpha-dependent induction of amphiregulin dampens myocardialischemia-reperfusion injury. Nat Commun 9 816 PMID: 29483579
Breshears et al (2012) A disintegrin and metalloproteinase 17 (ADAM17) and epidermal growth factor receptor (EGFR) signaling drive the epithelial response to Staphylococcus aureus toxic shock syndrome toxin-1 (TSST-1). J Biol Chem 287 32578 PMID: 22833676
Mathew et al (2015) Feedback circuitry between miR-218 repression and RTK activation in glioblastoma. Cell Death Dis 8 ra42 PMID: 25943352
Bertrand et al (2015) Conformations of tissue plasminogen activator (tPA) orchestrate neuronal survival by a crosstalk between EGFR and NMDAR. Sci Rep 6 e1924 PMID: 26469972
Pandya and Pillai (2014) TrkB interacts with ErbB4 and regulates NRG1-induced NR2B phosphorylation in cortical neurons before synaptogenesis. Sci Signal 12 47 PMID: 25052836
Breshears et al (2016) Local Epidermal Growth Factor Receptor Signaling Mediates the Systemic Pathogenic Effects of Staphylococcus aureus Toxic Shock Syndrome PLoS One 11 e0158969 PMID: 27414801
Maggiolini et al (2004) The G protein-coupled receptor GPR30 mediates c-fos up-regulation by 17beta-OE and phytoestrogens in breast cancer cells. J Biol Chem 279 27008 PMID: 15090535
Atherton et al (2003) IL-13-induced changes in the goblet cell density of human bronchial epithelial cell cultures: MAP kinase and phosphatidylinositol 3-kinase regulation. Am J Physiol Lung Cell Mol Physiol 285 L730 PMID: 12794003
Belcher et al (2005) Rapid estrogenic regulation of extracellular signal- regulated kinase 1/2 signaling in cerebellar granule cells involves a G protein- and protein kinase A-dependent mechanism and intracellular activation of protein phosphatase 2A. Endocrinology 146 5397 PMID: 16123167
Fang et al (2006) Resonant waveguide grating biosensor for living cell sensing. Biophys J 91 1925 PMID: 16766609
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It works great!.
By
Anonymous on 09/17/2022
分析类型： In Vitro
种属： Mouse
细胞系/组织： Cancer cells
PGE2 secretion was measured in mouse breast cancer cell lines and AG1478 significantly abolished the EGF-induced PGE2 secretion.
EGFR and MAPK inhibitor.
By
Anonymous on 03/10/2020
分析类型： In Vitro
种属： Human
细胞系/组织： Hepg2, Huh7
Used this inhibitor in 50nm for 24 hours and I found less activation of the MAPK pathway and cell growth and migration
serum-free media is working good for me
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