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L1635

Sigma-Aldrich

L-Leucine β-naphthylamide

Synonym(s):

L-Leucine-2-naphthylamide

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100 MG
¥9,120
1 G
¥28,800

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100 MG
¥9,120
1 G
¥28,800

About This Item

Empirical Formula (Hill Notation):
C16H20N2O
CAS Number:
732-85-4
Molecular Weight:
256.34
EC Number:
211-990-0
MDL number:
MFCD00055914
UNSPSC Code:
12352204
PubChem Substance ID:
24896286
NACRES:
NA.83

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Assay

≥98% (TLC)

form

powder

solubility

H2O: insoluble

storage temp.

−20°C

SMILES string

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

InChI key

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[1]
  • to evaluate the enzyme activity of cathepsin H from rabbit skeletal muscles[2]
  • in the proteolytic assay of L-Leucine aminopeptidase[3]

Substrate for leucine aminopeptidase determination in colorimetric and histochemical procedures.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Quality

Very low free β-naphthylamine.

Substrates

Substrate for aminopeptidase M

Pictograms

Health hazard
GHS08

Signal Word

Warning

Hazard Statements

H351

Precautionary Statements

P281

Hazard Classifications

Carc. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

L1635-BULK:
L1635-1G:
L1635-500MG:
L1635-250MG:
L1635-100MG:
L1635-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD2656
BCBS7416V
BCBN6521V
BCBK8465V
BCBG4407V

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J M de Gandarias et al.
Journal of biochemical toxicology, 7(3), 171-175 (1992-01-01)
Carbon disulfide, a volatile solvent, is widely used in industry. It has been demonstrated that it causes several neuropsychological symptoms. However, the neurochemical basis of its neurotoxic effect is relatively unknown. In this paper we have measured the effect of
A M Reisenauer et al.
Science (New York, N.Y.), 227(4682), 70-72 (1985-01-04)
The regulation of amino-oligopeptidase (AOP), an intestinal brush border hydrolase essential for the surface digestion of peptide nutrients, was examined in rats in vivo. Short-term (30-minute) intraintestinal perfusion of a tetrapeptide substrate, Gly-Leu-Gly-Gly, or a synthetic substrate, leucyl-beta-naphthylamide, induced a
Proteolytic activity in the placenta, decidua and postimplantation embryos of the rat.
A Fein et al.
Israel journal of medical sciences, 21(4), 394-396 (1985-04-01)
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
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
View All Related Papers

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