You Searched For: Glycine+iso-propyl+ester+hydrochloride+(H-Gly-OiPr.HCl)


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Supplier: APOLLO SCIENTIFIC
Description: Boc-D-Chg-OH 97%

Supplier: APOLLO SCIENTIFIC
Description: Boc-L-cyclopropylglycine

Supplier: SIGMA ALDRICH MICROSCOPY
Description: Schiff base which can be converted to amino alcohols and amino esters.

Supplier: BLD PHARMATECH GMBH
Description: Boc-L-cyclopropylglycine 97%

Supplier: Thermo Scientific
Description: Appearance: White Powder

Catalog Number: (H62914.03)
Supplier: Alfa Aesar
Description: Boc-L-cyclopropylglycine 95%
UOM: 1 * 1 g


Catalog Number: (ACRO361490010)
Supplier: Thermo Scientific
Description: Appearance: White Powder
UOM: 1 * 1 g


Catalog Number: (H52128.03)
Supplier: Alfa Aesar
Description: N-(tert-Butoxycarbonyl)-L-propargylglycine 95%
UOM: 1 * 1 g

Supplier: Alfa Aesar
Description: L-Cyclopropylglycine 97%

Supplier: APOLLO SCIENTIFIC
Description: N-(tert-Butoxycarbonyl)-L-propargylglycine 97%

Catalog Number: (BOSSBS-2976R-CY7)
Supplier: Bioss
Description: Cleaves the gamma-glutamyl bond of extracellular glutathione (gamma-Glu-Cys-Gly), glutathione conjugates, and other gamma-glutamyl compounds. The metabolism of glutathione releases free glutamate and the dipeptide, cysteinyl-glycine, which is hydrolyzed to cysteine and glycine by dipeptidases. In the presence of high concentrations of dipeptides and some amino acids, can also catalyze a transpeptidation reaction, transferring the gamma-glutamyl moiety to an acceptor amino acid to form a new gamma-glutamyl compound. Initiates extracellular glutathione (GSH) breakdown, provides cells with a local cysteine supply and contributes to maintain intracellular GSH level. It is part of the cell antioxidant defense mechanism. Isoform 3 seems to be inactive.
UOM: 1 * 100 µl


Catalog Number: (32999-25MG)
Supplier: Merck
Description: Organic Standard, Aminoethoxyvinyl glycine hydrochloride
UOM: 1 * 25 mg


Catalog Number: (BOSSBS-2976R-CY5)
Supplier: Bioss
Description: Cleaves the gamma-glutamyl bond of extracellular glutathione (gamma-Glu-Cys-Gly), glutathione conjugates, and other gamma-glutamyl compounds. The metabolism of glutathione releases free glutamate and the dipeptide, cysteinyl-glycine, which is hydrolyzed to cysteine and glycine by dipeptidases. In the presence of high concentrations of dipeptides and some amino acids, can also catalyze a transpeptidation reaction, transferring the gamma-glutamyl moiety to an acceptor amino acid to form a new gamma-glutamyl compound. Initiates extracellular glutathione (GSH) breakdown, provides cells with a local cysteine supply and contributes to maintain intracellular GSH level. It is part of the cell antioxidant defense mechanism. Isoform 3 seems to be inactive.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-2976R-CY5.5)
Supplier: Bioss
Description: Cleaves the gamma-glutamyl bond of extracellular glutathione (gamma-Glu-Cys-Gly), glutathione conjugates, and other gamma-glutamyl compounds. The metabolism of glutathione releases free glutamate and the dipeptide, cysteinyl-glycine, which is hydrolyzed to cysteine and glycine by dipeptidases. In the presence of high concentrations of dipeptides and some amino acids, can also catalyze a transpeptidation reaction, transferring the gamma-glutamyl moiety to an acceptor amino acid to form a new gamma-glutamyl compound. Initiates extracellular glutathione (GSH) breakdown, provides cells with a local cysteine supply and contributes to maintain intracellular GSH level. It is part of the cell antioxidant defense mechanism. Isoform 3 seems to be inactive.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-2976R-A750)
Supplier: Bioss
Description: Cleaves the gamma-glutamyl bond of extracellular glutathione (gamma-Glu-Cys-Gly), glutathione conjugates, and other gamma-glutamyl compounds. The metabolism of glutathione releases free glutamate and the dipeptide, cysteinyl-glycine, which is hydrolysed to cysteine and glycine by dipeptidases. In the presence of high concentrations of dipeptides and some amino acids, can also catalyse a transpeptidation reaction, transferring the gamma-glutamyl moiety to an acceptor amino acid to form a new gamma-glutamyl compound. Initiates extracellular glutathione (GSH) breakdown, provides cells with a local cysteine supply and contributes to maintain intracellular GSH level. It is part of the cell antioxidant defence mechanism. Isoform 3 seems to be inactive.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-2976R-A488)
Supplier: Bioss
Description: Cleaves the gamma-glutamyl bond of extracellular glutathione (gamma-Glu-Cys-Gly), glutathione conjugates, and other gamma-glutamyl compounds. The metabolism of glutathione releases free glutamate and the dipeptide, cysteinyl-glycine, which is hydrolyzed to cysteine and glycine by dipeptidases. In the presence of high concentrations of dipeptides and some amino acids, can also catalyze a transpeptidation reaction, transferring the gamma-glutamyl moiety to an acceptor amino acid to form a new gamma-glutamyl compound. Initiates extracellular glutathione (GSH) breakdown, provides cells with a local cysteine supply and contributes to maintain intracellular GSH level. It is part of the cell antioxidant defense mechanism. Isoform 3 seems to be inactive.
UOM: 1 * 100 µl


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
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