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首页- Products - Others - Other Targets - N-(3-Aminopropyl)cyclohexylamine

N-(3-Aminopropyl)cyclohexylamine

CAS No. 3312-60-5

N-(3-Aminopropyl)cyclohexylamine ( —— )

产品货号. M28059 CAS No. 3312-60-5

N-(3-Aminopropyl)cyclohexylamine, a cyclohexylamine derivative, acts as a selective and competitive inhibitor of spermidine synthase. N-(3-Aminopropyl)cyclohexylamine can be used for the research of neurological diseases.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
100MG ¥340 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
    N-(3-Aminopropyl)cyclohexylamine
  • 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
    N-(3-Aminopropyl)cyclohexylamine, a cyclohexylamine derivative, acts as a selective and competitive inhibitor of spermidine synthase. N-(3-Aminopropyl)cyclohexylamine can be used for the research of neurological diseases.
  • 产品描述
    N-(3-Aminopropyl)cyclohexylamine, a cyclohexylamine derivative, acts as a selective and competitive inhibitor of spermidine synthase. N-(3-Aminopropyl)cyclohexylamine can be used for the research of neurological diseases.(In Vitro):N-(3-Aminopropyl)cyclohexylamine at concentrations up to 10(-6) M did not affect the neuronal survival, but significantly blocked the survival-promoting effect of spermine (10(-8) M) . APCHA also blocked the spermine-induced promotion of neurite regeneration following axotomy . In primary cultured brain neurons, APCHA works as a spermine antagonist rather than as a spermine synthesis inhibitor .
  • 同义词
    ——
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    FPR1;FPR2
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    3312-60-5
  • 分子量
    156.3
  • 分子式
    C9H20N2
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    NCCCNC1CCCCC1
  • 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.Asahina Y, et al. Discovery of BMS-986235/LAR-1219: A Potent Formyl Peptide Receptor 2 (FPR2) Selective Agonist for the Prevention of Heart Failure [published online ahead of print, 2020 May 24]. J Med Chem. 2020;10.1021/acs.jmedchem.9b02101.
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