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Pyr10

CAS No. 1315323-00-2

Pyr10 ( —— )

产品货号. M22464 CAS No. 1315323-00-2

Pyr10 是一种吡唑衍生物,也是一种选择性 TRP 阳离子 3 抑制剂。 Pyr10 能够区分受体操作的 TRPC3 和天然基质相互作用分子 1 (STIM1)/Orai1 通道。 Pyr10 抑制卡巴胆碱刺激的 TRPC3 转染 HEK293 细胞中的 Ca2+ 流入(IC50:0.72 μM)(BRL-2H3 细胞中钙池操纵的 Ca2+ 进入的 IC50 为 13.08 μM)。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥437 有现货
10MG ¥721 有现货
50MG ¥2803 有现货
100MG 获取报价 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Pyr10
  • 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
    Pyr10 是一种吡唑衍生物,也是一种选择性 TRP 阳离子 3 抑制剂。 Pyr10 能够区分受体操作的 TRPC3 和天然基质相互作用分子 1 (STIM1)/Orai1 通道。 Pyr10 抑制卡巴胆碱刺激的 TRPC3 转染 HEK293 细胞中的 Ca2+ 流入(IC50:0.72 μM)(BRL-2H3 细胞中钙池操纵的 Ca2+ 进入的 IC50 为 13.08 μM)。
  • 产品描述
    Pyr10 is a pyrazole derivative and a selective TRP cation 3 inhibitor. Pyr10 has the ability to distinguish between receptor-operated TRPC3 and native stromal interaction molecule 1 (STIM1)/Orai1 channels. Pyr10 inhibits Ca2+ influx in carbachol-stimulated TRPC3-transfected HEK293 cells (IC50: 0.72 μM) (IC50 of 13.08 μM for store-operated Ca2+ entry in BRL-2H3 cells) . The novel pyrazole Pyr10 displayed substantial selectivity for TRPC3-mediated responses (18-fold) and the selective block of TRPC3 channels by Pyr10 barely affected mast cell activation.Pyr10 blunted ventricular CF activation and MF in l-NAME hypertensive mice.?Finally, TRPC3 was present in human ventricular CFs and upregulated in MF, whereas pharmacological modulation of TRPC3-NFATc3 decreased proliferation and collagen secretion.?TRPC3-NFATc3 signaling is modulated by P.E. and critically regulates ventricular CF phenotype and MF.?These findings strongly argue for P.E., through TRPC3 targeting, as potential and interesting therapeutics for MF management.
  • 体外实验
    Pyr10 has the ability to discriminate between the classical Orai-mediated, highly Ca2+ selective signalling pathway and the phospholipase C-dependent Ca2+ entry-mediated by TRPC channels, specifically by TRPC3. Pyr10 (3 μM) completely eliminates TRPC3 currents as well as Ca2+ entry while exerting modest effects on Orai-mediated responses. The selective block of TRPC3 channels by Pyr10 barely affected mast cell activation.
  • 体内实验
    Genetic deletion (TRPC3-/-) and pharmacological channel blockade with Pyr10 blunts ventricular cardiac fibroblast activation and myocardial fibrosis in N(ω)-nitro-l-arginine methyl ester (l-NAME) hypertensive mice.
  • 同义词
    ——
  • 通路
    Membrane Transporter/Ion Channel
  • 靶点
    TRP/TRPV Channel
  • 受体
    TRPC3
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    1315323-00-2
  • 分子量
    449.37
  • 分子式
    C18H13F6N3O2S
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:95 mg/mL (211.4 mM; Need ultrasonic)
  • SMILES
    Cc1ccc(cc1)S(=O)(=O)Nc1ccc(cc1)-n1nc(cc1C(F)(F)F)C(F)(F)F
  • 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. Schleifer H, et al. Novel pyrazole compounds for pharmacological discrimination between receptor-operated and store-operated Ca(2+) entry pathways. Br J Pharmacol. 2012 Dec;167(8):1712-1722.
产品手册
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