• 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

KH7

CAS No. 330676-02-3

KH7 ( KH-7;KH 7;sAC inhibitor KH7 )

产品货号. M14099 CAS No. 330676-02-3

A potent, specific soluble adenylyl cyclase (sAC) inhibitor that inhibits Mn2+-dependent sAC with IC50 of 2.7 uM.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥405 有现货
5MG ¥664 有现货
10MG ¥1069 有现货
25MG ¥2147 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
    KH7
  • 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
    A potent, specific soluble adenylyl cyclase (sAC) inhibitor that inhibits Mn2+-dependent sAC with IC50 of 2.7 uM.
  • 产品描述
    A potent, specific soluble adenylyl cyclase (sAC) inhibitor that inhibits Mn2+-dependent sAC with IC50 of 2.7 uM; inhibits physiologically stimulated sAC with similar potency with IC50 of 8.0 uM, completely blocks the capacitation-induced rise in cAMP in wild-type sperm at 10 uM, inhibits in vitro fertilization.
  • 同义词
    KH-7;KH 7;sAC inhibitor KH7
  • 通路
    Metabolic Enzyme/Protease
  • 靶点
    Adenylate Cyclase
  • 受体
    Adenylate Cyclase
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    330676-02-3
  • 分子量
    419.30
  • 分子式
    C17H15BrN4O2S
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO : ≥ 100 mg/mL 238.49 mM; H2O : < 0.1 mg/mL
  • SMILES
    CC(SC1=NC2=CC=CC=C2N1)C(N/N=C/C3=CC(Br)=CC=C3O)=O
  • 化学全称
    (E)-2-((1H-benzo[d]imidazol-2-yl)thio)-N'-(5-bromo-2-hydroxybenzylidene)propanehydrazide

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. Bitterman JL, et al. J Pharmacol Exp Ther. 2013 Dec;347(3):589-98.
2. Hess KC, et al. Dev Cell. 2005 Aug;9(2):249-59.
产品手册
关联产品
  • ST-034307

    ST-034307 (ST 034307, ST034307) is a potent, selective adenylyl cyclase 1 (AC1) with IC50 of 2.3 uM.

  • CB-7921220

    CB-7921220 is a potent, selective Adenylyl Cyclase 1 (AC1) inhibitor.

  • TIP 39, Tuberoinfund...

    This is a tuberoinfundibular neuropeptide and parathyroid hormone 2(PTH 2)-receptor agonist from hypothalmus. Synthetic TIP39 activates human and rat PTH2 receptors.