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L1635

Sigma-Aldrich

L-Leucine β-naphthylamide

Synonyme(s) :

L-Leucine-2-naphthylamide

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About This Item

Formule empirique (notation de Hill):
C16H20N2O
Numéro CAS:
732-85-4
Poids moléculaire :
256.34
Numéro CE :
211-990-0
Numéro MDL:
MFCD00055914
Code UNSPSC :
12352204
ID de substance PubChem :
24896286
Nomenclature NACRES :
NA.83

Pureté

≥98% (TLC)

Niveau de qualité

200

Forme

powder

Solubilité

H2O: insoluble

Température de stockage

−20°C

Chaîne SMILES 

CC(C)C[C@H](N)C(=O)Nc1ccc2ccccc2c1

InChI

1S/C16H20N2O/c1-11(2)9-15(17)16(19)18-14-8-7-12-5-3-4-6-13(12)10-14/h3-8,10-11,15H,9,17H2,1-2H3,(H,18,19)/t15-/m0/s1

Clé InChI

JWHURRLUBVMKOT-HNNXBMFYSA-N

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Application

L-Leucine β-naphthylamide has been used as a substrate:
  • to measure the activity of aminopeptidase in Escherichia coli
  • to evaluate the enzyme activity of cathepsin H from rabbit skeletal muscles
  • in the proteolytic assay of L-Leucine aminopeptidase

Substrate for leucine aminopeptidase determination in colorimetric and histochemical procedures.

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Qualité

Very low free β-naphthylamine.

Substrats

Substrate for aminopeptidase M

Pictogrammes

Health hazard
GHS08

Mention d'avertissement

Warning

Mentions de danger

H351

Conseils de prudence

P281

Classification des risques

Carc. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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H Yokozeki et al.
The American journal of physiology, 252(6 Pt 2), R1119-R1129 (1987-06-01)
Attempts were made to purify and characterize cysteine proteinases in human eccrine sweat and further clarify their origin. Benzoyl-DL-arginine-beta-naphthylamide (BANA) and L-leucine beta-naphthylamide (LeuNA) hydrolases in thermally induced sweat were sequentially purified by Sephacryl S-200 chromatography and chromatofocusing, which yielded
Nikou Hesari et al.
Enzyme and microbial technology, 83, 22-28 (2016-01-19)
There remains a need for rapid, specific and sensitive assays for the detection of bacterial indicators for water quality monitoring. In this study, a strategy for rapid detection of Escherichia coli in drinking water has been developed. This strategy is
F Alba et al.
Life sciences, 43(11), 935-939 (1988-01-01)
Levels of soluble aminopeptidase (AP), measured as arylamidase activity using L-Leucine-2-Naphthylamide (Leu-2-NA) as substrate, were determined in the soluble fraction of eleven zones of rat brain. Results showed that AP activity is asymmetrically distributed in frontal cortex and hypothalamus with
R Alidina et al.
Experimental and molecular pathology, 49(1), 118-127 (1988-08-01)
Squamous cell carcinomas (SCC) were experimentally produced in hairless mouse skin, and cysteine protease and its inhibitor were simultaneously purified from extracts of 1 g of tissue of SCC and normal skin. Activity of cysteine proteinases, Mr greater than 50,000
Mohamad Elzein et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 48(8), 925-932 (2013-03-15)
The objective of the study was to identify the enzymatic-biochemical (enz-bio) signatures of Escherichia coli and Salmonella for rapid detection of these bacteria in drinking water biofilms. The relative potency of lipophilic, glucosidic, and proteolytic activities in biofilms containing single
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