相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
4°C, sealed storage, away from moisture
- 英文名:
AC480 Hydrochloride
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
873837-23-1
- 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: | ¥1044.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥680.0 |
| 规格: | 10 mg | 产品价格: | ¥1050.0 |
| 规格: | 25 mg | 产品价格: | ¥2076.0 |
| 规格: | 50 mg | 产品价格: | ¥3580.0 |
| 规格: | 100 mg | 产品价格: | ¥4960.0 |
MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务。
BMS-599626 Hydrochloride
CAS No. : 873837-23-1
MCE 国际站:BMS-599626 Hydrochloride
产品活性:BMS-599626 Hydrochloride (AC480 Hydrochloride) 是一种选择性的口服生物利用度 HER1 和 HER2 抑制剂,其 IC50 分别为 20和 30 nM。BMS-599626 Hydrochloride 对 HER4 的 IC50 值为 190 nM,对 VEGFR2、c-Kit、Lck、MEK的抑制强度降低了 100 倍。BMS-599626 Hydrochloride 抑制肿瘤细胞增殖,并有可能增加肿瘤对放疗的反应。
研究领域:JAK/STAT Signaling | Protein Tyrosine Kinase/RTK
作用靶点:EGFR
In Vitro: BMS-599626 Hydrochloride inhibits the proliferation of tumor cells that are dependent on HER1/HER2 signaling.BMS-599626 Hydrochloride (0.03-8 μM; 1 huors) results in the inhibition of receptor autophosphorylation, as well as MAPK phosphorylation, with IC50s of 0.3 and 0.22 μM, respectively, in Sal2 cells which express a CD8HER2 fusion protein.
BMS-599626 Hydrochloride abrogates HER1 and HER2 signaling and inhibited the proliferation of tumor cell lines that are dependent on these receptors, with IC50s in the range of 0.24 to 1 μM.In GEO cells, HER1 phosphorylation is stimulated by treatment with EGF and is inhibited by BMS-599626 Hydrochloride (IC50=0. 75 μM).There is also nearly complete inhibition of EGF-dependent MAPK (0. 8 μM) but only partial inhibition of AKT signaling.The latter likely reflects the activation of AKT by multiple upstream signals.Treatment of N87 cells with BMS-599626 Hydrochloride leads to the inhibition of HER2 (0. 38 μM), which is expressed to a high level because of gene amplification, as well as MAPK and AKT phosphorylation (0.35 μM for both).
At the molecular level, in HN-5 cells the agent (BMS-599626 Hydrochloride) inhibits the expression of pEGFR, pHER2, cyclins D and E, pRb, pAkt, pMAPK, pCDK1 and 2, CDK 6, and Ku70 proteins. BMS-599626 Hydrochloride also induced accumulation of cells in the G1 cell cycle phase, inhibited cell growth, enhanced radiosensitivity, and prolonged the presence of γ-H AX foci up to 24 h after radiation.
In Vivo: BMS-599626 Hydrochloride (60-240 mg/kg; p.o.; daily for 14 days) results in a dose-dependent inhibition of Sal2 tumor growth.
BMS-599626 Hydrochloride treatment results in the inhibition of GEO xenograft tumor growth when given once daily for 14 days. In addition to efficacy in the Sal2, GEO, and KPL4 models, BMS-599626 has similar antitumor activity in other HER2 amplified xenograft models including the BT474 breast and N87 gastric tumors, as well as other HER1-overexpressing non-small-cell lung tumors (A549 and L2987).
BMS-599626 Hydrochloride given before and during irradiation improved the radioresponse of HN5 tumors in vivo.
相关产品:Clinical Compound Library Plus | Bioactive Compound Library Plus | Immunology/Inflammation Compound Library | JAK/STAT Compound Library | Kinase Inhibitor Library | Protein Tyrosine Kinase Compound Library | Anti-Cancer Compound Library | Clinical Compound Library | Differentiation Inducing Compound Library | Orally Active Compound Library | Anti-Hepatitis C Virus Compound Library | Anti-Lung Cancer Compound Library | Anti-Pancreatic Cancer Compound Library | Gefitinib | Trastuzumab | Erlotinib | Cetuximab | AG490 | Genistein | AG-1478 | Pertuzumab | BI-4020 | NSC 228155 | Pelitinib | Mubritinib | TX1-85-1 | AZ7550 hydrochloride | Butein | PD168393 | AEE788 | Canertinib dihydrochloride | Daphnetin | EGFR-IN-7 | Chrysophanol | PD153035 | Tyrphostin 23 | Trastuzumab emtansine | Falnidamol | Lavendustin A
品牌介绍:
• MCE (MedChemExpress) 拥有数百种全球独家化合物,我们致力于为全球科研客户提供前沿最全的高品质小分子活性化合物;
• 10,000 多种高选择性抑制剂、激动剂涉及各热门信号通路及疾病领域;
• 设有专业的实验中心和严格的质控、验证体系;
• 提供 LC/MS、NMR、HPLC、手性分析、元素分析等各项质检报告,确保产品的高纯度、高品质;
• 产品的生物活性多经各国客户实验验证;
• Nature, Cell, Science 等多种TOP期刊及制药专利收录了MCE客户的科研成果;
• 专业团队跟踪前沿的制药及生命科学研究进展,为您提供全球前沿的活性化合物;
• 与世界各大制药公司及知名科研机构建立了长期的合作。
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验Lacrimal Experimental Protocol (4/4/94)
up to 8 ml. 23. Incubate at 37°C on vortex for 15 min. 24. In inhibition experiments, add 50 µg/well antibody to BMS for 1 hr at 37°C. 25. Transfer to 15 ml conical. Wash flask out two times with DMEM/STI/gent and spin at 500 rpm for 3 min
Signal Transduction Inhibitors in Cellular Function
BMS-182878, BMS-184467 (57 –59) Inhibitors of the Raf protein kinases ISIS5132, BAY43-9006 (57 –59
, Evodia rutaecarpa Gliotoxin, Gladiocladium fimbriatum Hypoestoxide, Hypoestes rosea I kappaB Kinase Inactive Control Peptide, Cell-Permeable I kappaB Kinase Inhibitor Peptide, Cell-Permeable IKK Inhibitor III, BMS-345541 IKK
技术资料暂无技术资料 索取技术资料

















