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L-Leucine7-amido-4-methylcoumarinhydrochloride

L-Leucine 7-amido-4-methylcoumarin hydrochloride; L-Leucine (4-methyl-7-coumarinylamide) hydrochloride; H-Leu-AMC ? HCl Fluorogenic substrate for leucine aminop…

L-Leucine7-amido-4-methylcoumarinhydrochloride
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  • ISO 9001:2015 facilities · CoA + batch tracking with every shipment
  • Worldwide shipping · dry-ice option for thermolabile reagents
  • Research Use Only — not for human or veterinary clinical use

About this product

L-Leucine 7-amido-4-methylcoumarin hydrochloride; L-Leucine (4-methyl-7-coumarinylamide) hydrochloride; H-Leu-AMC ? HCl Fluorogenic substrate for leucine aminopeptidase. L-Leu-AMC is a fluorogenic substrate for leucine aminopeptidase. Upon enzymatic cleavage by leucine aminopeptidase, AMC is released and its fluorescence can be used to quantify leucine aminopeptidase activity. AMC displays excitation/emission maxima of 340-360/440-460 nm, respectively. L-Leucine 7-Amido-4-methylcoumarin Hydrochloride is a fluorogenic substrate for LAP3 (leucine aminopeptidase). Upon enzyme activity, a bright blue fluorescent dye, 7-amino-4-methylcoumarin, is released. L-Leucine 7-amido-4-methylcoumarin hydrochloride salt is a protease inhibitor that has been shown to inhibit the activity of serine proteases. It has been shown to have potential as a drug target, and has also been shown to be effective in wastewater treatment. The biochemical properties of L-Leucine 7-amido-4-methylcoumarin hydrochloride salt have been investigated using sephadex G-100 chromatography and phosphatase activity assays. This molecule has also been shown to affect physiological function and enzyme activities in rats. L-Leucine 7-amido-4-methylcoumarin hydrochloride salt is metabolized by microbial enzymes, such as proteases, which may produce ATP as an energy source. CAS Number 62480-44-8 Product Name L-Leucine-7-amido-4-methylcoumarin hydrochloride IUPAC Name (2S)-2-amino-4-methyl-N-(4-methyl-2-oxochromen-7-yl)pentanamide;hydrochloride Molecular Formula C16H20N2O3*HCl Molecular Weight 324,8 g/mole InChI InChI=1S/C16H20N2O3.ClH/c1-9(2)6-13(17)16(20)18-11-4-5-12-10(3)7-15(19)21-14(12)8-11;/h4-5,7-9,13H,6,17H2,1-3H3,(H,18,20);1H/t13-;/m0./s1 SMILES CC1=CC(=O)OC2=C1C=CC(=C2)NC(=O)C(CC(C)C)N.Cl

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