• 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

ST-034307

CAS No. 133406-29-8

ST-034307 ( ST 034307;ST034307 )

产品货号. M11327 CAS No. 133406-29-8

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

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥365 有现货
5MG ¥599 有现货
10MG ¥948 有现货
25MG ¥2009 有现货
50MG ¥3451 有现货
100MG ¥5119 有现货
500MG ¥10935 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    ST-034307
  • 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
    ST-034307 (ST 034307, ST034307) is a potent, selective adenylyl cyclase 1 (AC1) with IC50 of 2.3 uM.
  • 产品描述
    ST-034307 (ST 034307, ST034307) is a potent, selective adenylyl cyclase 1 (AC1) with IC50 of 2.3 uM; shows no activity against other AC isoforms; inhibits Ca2+-stimulated cAMP accumulation in HEK cells, also inhibits AC1 activity stimulated by forskolin- and Gαs-coupled receptors in HEK-AC1 cells; reduces pain responses in a mouse model of inflammatory pain.
  • 同义词
    ST 034307;ST034307
  • 通路
    Metabolic Enzyme/Protease
  • 靶点
    Adenylate Cyclase
  • 受体
    Adenylate Cyclase
  • 研究领域
    Neurological Disease
  • 适应症
    ——

化学信息

  • CAS Number
    133406-29-8
  • 分子量
    297.95
  • 分子式
    C10H4Cl4O2
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO : 50 mg/mL 167.81 mM
  • SMILES
    O=C1C=C(C(Cl)(Cl)Cl)OC2=C1C=C(Cl)C=C2
  • 化学全称
    6-chloro-2-(trichloromethyl)-4H-chromen-4-one

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. Brust TF, et al. Sci Signal. 2017 Feb 21;10(467). pii: eaah5381.
产品手册
关联产品
  • NB 001

    A potent, relatively selective and orally active adenylyl cyclase 1 (AC1) inhibitor with IC50 of 10 uM (cAMP production inhibition).

  • SQ-22536

    A potent, non-competitive Adenylyl Cyclase inhibitor with IC50 of 1.4 uM.

  • 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.