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L1635
L-Leucine β-naphthylamide
Synonym(e):
L-Leucine-2-naphthylamide
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About This Item
Empfohlene Produkte
Assay
≥98% (TLC)
Qualitätsniveau
Form
powder
Löslichkeit
H2O: insoluble
Lagertemp.
−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
InChIKey
JWHURRLUBVMKOT-HNNXBMFYSA-N
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Anwendung
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.
Verpackung
Bottomless glass bottle. Contents are inside inserted fused cone.
Qualität
Very low free β-naphthylamine.
Substrate
Substrate for aminopeptidase M
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Proteolytic activity in the placenta, decidua and postimplantation embryos of the rat.
Israel journal of medical sciences, 21(4), 394-396 (1985-04-01)
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
European journal of biochemistry, 137(1-2), 23-27 (1983-12-01)
The mode of action towards oligopeptides and proteins of hydrolase H purified from rabbit skeletal muscle was studied. The presence of protamine or alpha-N-benzoylarginine p-nitroanilide (an endopeptidase substrate) changed both the Km and V values of the enzyme towards Leu-beta-naphthylamide
Aminopeptidase (arylamidase) activity in discrete areas of the rat brain: sex differences.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme, 21(5), 285-286 (1989-05-01)
The international journal of biochemistry & cell biology, 35(4), 474-485 (2003-02-05)
Rabbit muscle cathepsin H classified as an aminoendopeptidase was purified and its properties were investigated to clarify its contribution to the proteolysis of postmortem muscle. The purification was performed by ammonium sulfate fractionation and successive chromatographies on Sephadex G-75, phosphocelluose
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