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BMS-599626,873837-23-1

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  • ¥680 - 4960
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  • 美国
  • HY-12010
  • 2025年12月05日
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    • 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 HER1HER2 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

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    图标文献和实验
    相关实验
    • 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

    • 【求助】关于NFkB抑制剂

      , Evodia rutaecarpa Gliotoxin, Gladiocladium fimbriatum Hypoestoxide, Hypoestes rosea I kappaB Kinase Inactive Control Peptide, Cell-Permeable I kappaB Kinase Inhibitor Peptide, Cell-Permeable IKK Inhibitor III, BMS-345541 IKK

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