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
Size | Price / USD | Stock | Quantity |
100MG | 38 | Get Quote |
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200MG | Get Quote | Get Quote |
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500MG | Get Quote | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameN-(3-Aminopropyl)cyclohexylamine
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NoteResearch use only, not for human use.
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Brief DescriptionN-(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.
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DescriptionN-(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 .
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorFPR1;FPR2
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Research Area——
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Indication——
Chemical Information
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CAS Number3312-60-5
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Formula Weight156.3
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Molecular FormulaC9H20N2
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Purity>98% (HPLC)
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Solubility——
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SMILESNCCCNC1CCCCC1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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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