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Progabide

CAS No. 62666-20-0

Progabide ( SL 76002 | Halogabide | Gabren | Gabrene )

产品货号. M26795 CAS No. 62666-20-0

Progabide 是 γ-氨基丁酸受体的激动剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥381 有现货
10MG ¥648 有现货
25MG ¥1320 有现货
50MG ¥2130 有现货
100MG ¥3345 有现货
200MG ¥4779 有现货
500MG ¥7638 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Progabide
  • 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
    Progabide 是 γ-氨基丁酸受体的激动剂。
  • 产品描述
    Progabide is an agonist of the gamma-aminobutyric acid receptor.(In Vivo):Progabide ( 50, 100 and 200 mg/kg) given IP to male Wistar rats enhance the plasma corticosterone levels by 244, 365, and 476% respectively (t=6.44 to12.55, p<0.01). Progabide (10 mg/kg) fails to change the concentration of corticosterone in plasma (t=0.76, N.S.). The increased plasma corticosterone level induced by administration of 200 mg/kg Progabide is evident 30 (t=2.625, p<0.05), 60 (t=13.13, p<0.001) and 120 min (t=4.07, p<0.01) after drug injection, but returns to the control value 240 min after drug injection (t=0.86, N.S.). Compare with the corresponding control, The greatest corticosterone rise is reached 60 min following the administration of Progabide.
  • 体外实验
    ——
  • 体内实验
    Progabide is a gamma-aminobutyric acid receptor (GABA) agonist. Doses of 50, 100 and 200 mg/kg Progabide given IP to male Wistar rats increase the plasma corticosterone levels by 244, 365 and 476% respectively (t=6.44 to12.55, p<0.01). 10 mg/kg of Progabide fails to change the concentration of corticosterone in plasma (t=0.76, N.S.). The increased plasma corticosterone level induced by administration of 200 mg/kg Progabide is evident 30 (t=2.625, p<0.05), 60 (t=13.13, p<0.001) and 120 min (t=4.07, p<0.01) after drug injection, but returns to the control value 240 min after drug injection (t=0.86, N.S.). The greatest corticosterone rise (compare with the corresponding control) is reached 60 min following the administration of Progabide.
  • 同义词
    SL 76002 | Halogabide | Gabren | Gabrene
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    Kv2.2
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    62666-20-0
  • 分子量
    334.78
  • 分子式
    C17H16ClFN2O2
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 250 mg/mL (746.78 mM)
  • SMILES
    NC(=O)CCC\N=C(\c1ccc(Cl)cc1)c1cc(F)ccc1O
  • 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.Herrington J, et al. Identification of novel and selective Kv2 channel inhibitors. Mol Pharmacol. 2011 Dec;80(6):959-64.
产品手册
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