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L8250

DL-Leucinamide hydrochloride

Name: <SC>DL</SC>-Leucinamide hydrochloride
Brand: SIGMA

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About This Item

Formule empirique (notation de Hill):

C₆H₁₄N₂O · HCl

Numéro CAS:

10466-60-1

Poids moléculaire :

166.65

Numéro MDL:

MFCD00070244

Code UNSPSC :

12352200

ID de substance PubChem :

24896497

Pureté

≥98% (TLC)

Forme

powder

Couleur

white

Chaîne SMILES

Cl.CC(C)CC(N)C(N)=O

InChI

1S/C6H14N2O.ClH/c1-4(2)3-5(7)6(8)9;/h4-5H,3,7H2,1-2H3,(H2,8,9);1H

Clé InChI

VSPSRRBIXFUMOU-UHFFFAOYSA-N

Actions biochimiques/physiologiques

DL-Leucinamide hydrochloride is a racemic mixture of D- and L- enantiomers of leucinamide. Leucinamide is an amide derivative of leucine found at the C-terminal of various peptides such as the PAR-2 activating peptide SLIGRL-NH(2).

Code de la classe de stockage

13 - Non 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 N95 (US)

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L: -Stereoselective amino acid amidase with broad substrate specificity from Brevundimonas diminuta: characterization of a new member of the leucine aminopeptidase family.

Hidenobu Komeda et al.

Applied microbiology and biotechnology, 70(4), 412-421 (2005-07-08)

Brevundimonas diminuta TPU 5720 produces an amidase acting L-stereoselectively on phenylalaninamide. The enzyme (LaaA(Bd)) was purified to electrophoretic homogeneity by ammonium sulfate fractionation and four steps of column chromatography. The final preparation gave a single band on SDS-PAGE with a

Molecular mechanism of the inhibitory effect of cobalt ion on thermolysin activity and the suppressive effect of calcium ion on the cobalt ion-dependent inactivation of thermolysin.

Yasuhiko Hashida et al.

Journal of biochemistry, 141(6), 879-888 (2007-04-05)

Thermolysin activity in the hydrolysis of N-[3-(2-furyl)acryloyl]-glycyl-l-leucine amide (FAGLA) and FA-l-leucyl-l-alanine amide (FALAA) was examined at various Co(2+) and Ca(2+) concentrations. It decreased to 28% with increasing [Co(2+)] up to 18 mM. The Co(2+)-dependent inactivation was in part suppressed by

Application of Fourier transform infrared spectroscopy for monitoring hydrolysis and synthesis reactions catalyzed by a recombinant amidase.

R Pacheco et al.

Analytical biochemistry, 346(1), 49-58 (2005-09-28)

This study demonstrates the use of Fourier transform infrared (FTIR) spectroscopy for monitoring both synthesis and hydrolysis reactions catalyzed by a recombinant amidase (EC 3.5.1.4) from Pseudomonas aeruginosa. The kinetics of hydrolysis of acetamide, propionamide, butyramide, acrylamide, benzamide, phenylalaninamide, alaninamide

Activation of PAR-2 elicits NO-dependent and CGRP-independent dilation of the dural artery.

Deepak K Bhatt et al.

Headache, 50(6), 1017-1030 (2010-05-22)

The goal of this study was to determine the vascular effects of protease-activated receptor-2 (PAR-2) activation in the rat cranial vasculature. The role of PAR-2 in pain and inflammatory conditions has been established but the information available on its effects

Formation of diastereomeric derivatives of 2-arylpropionic acids using L-leucinamide: lack of generality.

R Mehvar et al.

Journal of chromatography, 431(1), 228-230 (1988-09-23)

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