• 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
首页- Products - Others - Other Targets - 3-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride

3-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride

CAS No. 937724-81-7

3-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride ( —— )

产品货号. M28992 CAS No. 937724-81-7

3-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride can be used in the synthesis of piperidin-4-yl-urea derivatives which are MCH-R1 antagonists.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥3540 有现货
10MG ¥5233 有现货
25MG ¥7995 有现货
50MG ¥11178 有现货
100MG ¥15066 有现货
500MG ¥30132 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    3-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride
  • 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
    3-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride can be used in the synthesis of piperidin-4-yl-urea derivatives which are MCH-R1 antagonists.
  • 产品描述
    3-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride can be used in the synthesis of piperidin-4-yl-urea derivatives which are MCH-R1 antagonists.
  • 同义词
    ——
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    CYP3A4
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    937724-81-7
  • 分子量
    218.7
  • 分子式
    C10H19ClN2O
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    Cl.O=C(C1CCCNC1)N1CCCC1
  • 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.Robert L Walsky, et al. Selective mechanism-based inactivation of CYP3A4 by CYP3cide (PF-04981517) and its utility as an in vitro tool for delineating the relative roles of CYP3A4 versus CYP3A5 in the metabolism of drugs. Drug Metab Dispos. 2012 Sep;40(9)
产品手册
关联产品
  • OD1

    Potent rat Nav1.7, human Nav1.4 and rat Nav1.6 channel activator (EC50 values are 7, 10 and 47 nM, respectively). Exhibits minimal activation at mammalian Nav1.2, Nav1.3 and Nav1.5 (EC50 values >3 μM). Inhibits fast inactivation on all channels. Increases peak currents at all voltages and stimulates a persistent Na+ current at hNav1.7 channel. Increases hyperpolarization at Nav1.4 and Nav1.6 channels. Induces spontaneous pain in vivo.

  • Neoorthosiphol A

    Neoorthosiphol A is a natural product for research related to life sciences.

  • DHODH-IN-4

    DHODH-IN-4 is a human and Plasmodium falciparum dihydroorotate dehydrogenase (DHODH) inhibitor.