• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Wy 49051

CAS No. 113418-56-7

Wy 49051 ( Wy-49051 )

产品货号. M26508 CAS No. 113418-56-7

Wy 49051 is an orally active antagonist of H1 receptor(IC50 of 44 nM).

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥4026 有现货
10MG ¥5856 有现货
25MG ¥9153 有现货
50MG ¥12312 有现货
100MG ¥16038 有现货
500MG ¥32157 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Wy 49051
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Wy 49051 is an orally active antagonist of H1 receptor(IC50 of 44 nM).
  • 产品描述
    Wy 49051 is an orally active antagonist of H1 receptor(IC50 of 44 nM).(In Vitro):Wy 49051 showed a great inhibitory effect on H1. At a concentration of 100 nM, it produced 92% inhibition of histamine-induced guinea pig ileal contraction. Wy 49051 is the most effective compound, with 700 times the potency of astemizole and 470 times the potency of hydroquinone. Wy 49051 also has high affinity for α1 receptor with IC50 of 8 nM.(In Vivo):Wy 49051 shows against histamine-induced lethality in the guinea pig(ED50 of 1.91 mg/kg by po, 0.70 mg/kg by ip, and 0.01 mg/kg by iv). The duration of action of 24 is also favorable since there is no decrease in oral efficacy up to 18 h posttreatment.
  • 同义词
    Wy-49051
  • 通路
    Angiogenesis
  • 靶点
    ALK
  • 受体
    Arenavirus
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    113418-56-7
  • 分子量
    487.6
  • 分子式
    C28H33N5O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    Cn1c2ncn(CCCN3CCC(CC3)OC(c3ccccc3)c3ccccc3)c2c(=O)n(C)c1=O
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Carney DW, et al. Structural optimization of a retrograde trafficking inhibitor that protects cells from infections by human polyoma- and papillomaviruses. Bioorg Med Chem. 2014 Sep 1;22(17):4836-47.
产品手册
关联产品
  • GSK1838705A

    GSK1838705A is a potent, specific inhibitor of IGF-IR and insulin receptor (IR) with IC50 of 2.0 and 1.6 nM.

  • CPI-169

    CPI-169 is a potent, and selective EZH2 inhibitor with IC50 of 0.24 nM, 0.51 nM, and 6.1 nM for EZH2 WT, EZH2 Y641N, and EZH1, respectively.

  • LDN212854

    LDN-212854 is a novel BMP inhibitor that exhibits substantially greater selectivity for BMP versus the TGF-β type I receptors.