الصفحة الرئيسية>>Signaling Pathways>> Proteases>> Aminopeptidase>>L-Leucine 4-methoxy-β-naphthylamide (hydrochloride)

L-Leucine 4-methoxy-β-naphthylamide (hydrochloride) (Synonyms: Leu-MNA)

رقم الكتالوجGC13454

substrate for aminopeptidase M and leucine aminopeptidase

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L-Leucine 4-methoxy-β-naphthylamide (hydrochloride) التركيب الكيميائي

Cas No.: 4467-68-9

الحجم السعر المخزون الكميّة
100mg
94٫00
متوفر
250mg
221٫00
متوفر
1g
741٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description of L-Leucine 4-methoxy-β-naphthylamide (hydrochloride)

L-Leucine 4-methoxy-β-naphthylamide is a substrate for aminopeptidase M and leucine aminopeptidase.

Aminopeptidases are enzymes catalyzing the cleavage of amino acids from the amino terminus (N-terminus) of proteins or peptides. Aminopeptidases are distributed widely throughout the animal and plant kingdoms and are present in various subcellular organelles, in cytosol, as well as membrane components.

In vitro: L-Leucine 4-methoxy-β-naphthylamide was identified as a cell-permeable substrate for aminopeptidase M and leucine aminopeptidase that was developed for intracellular analysis of protease activities [1]. In a previous method-developing study, peptide derivatives of 4-methoxy-β-naphthylamine including L-leucine 4-methoxy-β-naphthylamide were incubated in microtiter plates together with nitrosalicylaldehyde. Selectivity was achieved by running parallel assays containing inhibitors partially selective for each of peptide derivatives. This method was successfully validated by measurements in cells isolated from cathepsin B-/--, K-/--, and L-/-- mice [2].

In vivo: Up to now, there is no animal in vivo data reported.

Clinical trial: So far, no clinical study has been conducted.

References:
[1] Monis, B. ,Wasserkrug, H. and Seligman, A.M. Comparison of fixatives and substrates for aminopeptidase. Journal of Histochemistry and Cytochemistry 13(6), 503-509 (1965).
[2] Rüttger, A. ,Mollenhauer, J.,Lser, R., et al. Microplate assay for quantitative determination of cathepsin activities in viable cells using derivatives of 4-methoxy-β-naphthylamide. Biotechniques 41(4), 469-473 (2006).

Chemical Properties of L-Leucine 4-methoxy-β-naphthylamide (hydrochloride)

Cas No. 4467-68-9 SDF
المرادفات Leu-MNA
Chemical Name (S)-2-amino-N-(4-methoxy-2-naphthalenyl)-4-methyl-pentanamide, monohydrochloride
Canonical SMILES COC1=CC(NC([C@H](CC(C)C)N)=O)=CC2=CC=CC=C21.Cl
Formula C17H22N2O2 • HCl M.Wt 322.8
الذوبان ≤25mg/ml in ethanol;10mg/ml in DMSO;20mg/ml in dimethyl formamide Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of L-Leucine 4-methoxy-β-naphthylamide (hydrochloride)

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 3.0979 mL 15.4895 mL 30.9789 mL
5 mM 0.6196 mL 3.0979 mL 6.1958 mL
10 mM 0.3098 mL 1.5489 mL 3.0979 mL
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In vivo Formulation Calculator (Clear solution) of L-Leucine 4-methoxy-β-naphthylamide (hydrochloride)

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
3. All of the above co-solvents are available for purchase on the GlpBio website.

Product Documents

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