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NVP-BAW2881,861875-60-7

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  • ¥500 - 4400
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-100394
  • 2025年12月05日
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    • 详细信息
    • 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.

    • 英文名

      BAW2881

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • 规格

      10 mM * 1 mL/2 mg/5 mg/10 mg/25 mg/50 mg

    规格:10 mM * 1 mL产品价格:¥747.0
    规格:2 mg产品价格:¥500.0
    规格:5 mg产品价格:¥800.0
    规格:10 mg产品价格:¥1400.0
    规格:25 mg产品价格:¥2700.0
    规格:50 mg产品价格:¥4400.0

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    NVP-BAW2881

    CAS No. : 861875-60-7

    MCE 国际站:NVP-BAW2881

    产品活性:NVP-BAW2881 (BAW2881) 是有效,选择性的 VEGFR2 抑制剂,IC50 为值9 nM。

    研究领域:Protein Tyrosine Kinase/RTK

    作用靶点:Tie  |  VEGFR

    In Vitro: The VEGF-driven cellular receptor autophosphorylation in CHO cells of BAW2881 is inhibited with an IC50 of 4 nM. BAW2881 inhibits a limited number of kinases including c-RAF, B-RAF, RET, ABL, and TIE-2 at sub-μM IC50s. NVP-BAW2881 is highly selective for VEGFR, although it also demonstrates activity against Tie2 (IC50=650 nM) and RET (IC50=410 nM). The IC50 values of NVP-BAW2881 toward a wide panel of other kinases are >10 μM. NVP-BAW2881 inhibits VEGF-A-induced phosphorylation of VEGFR-2 in HUVECs and in VEGFR-2-transfected Chinese hamster ovary cells, with IC50 values of 2.9 and 4.2 nM, respectively.

    In Vivo: In a transgenic mouse model of psoriasis, NVP-BAW2881 reduces the number of blood and lymphatic vessels and infiltrating leukocytes in the skin, and normalized the epidermal architecture. NVP-BAW2881 also displays strong anti-inflammatory effects in models of acute inflammation; pretreatment with topical NVP-BAW2881 significantly inhibits VEGF-A-induced vascular permeability in the skin of pigs and mice.

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