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N-(3-Aminopropyl)cyclohexylamine

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Catalog No. T35878Cas No. 3312-60-5

N-(3-Aminopropyl)cyclohexylamine, a derivative of cyclohexylamine, acts as a selective and competitive inhibitor of spermine synthase, making it suitable for research on neurological diseases [1].

N-(3-Aminopropyl)cyclohexylamine

N-(3-Aminopropyl)cyclohexylamine

🥰Excellent
Purity: 98.82%
Catalog No. T35878Cas No. 3312-60-5
N-(3-Aminopropyl)cyclohexylamine, a derivative of cyclohexylamine, acts as a selective and competitive inhibitor of spermine synthase, making it suitable for research on neurological diseases [1].
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100 mg$42In Stock
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Purity:98.82%
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Product Introduction

Bioactivity
Description
N-(3-Aminopropyl)cyclohexylamine, a derivative of cyclohexylamine, acts as a selective and competitive inhibitor of spermine synthase, making it suitable for research on neurological diseases [1].
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) [1]. APCHA also blocked the spermine-induced promotion of neurite regeneration following axotomy [1]. In primary cultured brain neurons, APCHA works as a spermine antagonist rather than as a spermine synthesis inhibitor [1].
Chemical Properties
Molecular Weight156.2685
FormulaC9H20N2
Cas No.3312-60-5
SmilesNCCCNC1CCCCC1
Relative Density.0.917 g/cm3 at 25℃ (lit.)
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 95 mg/mL (607.92 mM), Sonication is recommended.
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM6.3992 mL31.9962 mL63.9924 mL319.9621 mL
5 mM1.2798 mL6.3992 mL12.7985 mL63.9924 mL
10 mM0.6399 mL3.1996 mL6.3992 mL31.9962 mL
20 mM0.3200 mL1.5998 mL3.1996 mL15.9981 mL
50 mM0.1280 mL0.6399 mL1.2798 mL6.3992 mL
100 mM0.0640 mL0.3200 mL0.6399 mL3.1996 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
1 Enter information below:
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2 Enter the in vivo formulation:
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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