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N-(3-Aminopropyl)cyclohexylamine

CAS No. 3312-60-5

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

Catalog No. 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.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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100MG 38 Get Quote
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Biological Information

  • Product Name
    N-(3-Aminopropyl)cyclohexylamine
  • Note
    Research use only, not for human use.
  • Brief Description
    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.
  • Description
    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 .
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    FPR1|FPR2
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    3312-60-5
  • Formula Weight
    156.273
  • Molecular Formula
    C9H20N2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?H2O : 100 mg/mL (639.92 mM)
  • SMILES
    NCCCNC1CCCCC1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

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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