You Searched For: 3,5-Dichloro-L-phenylalanine


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Catalog Number: (APOSPC430503-2G)
Supplier: Apollo Scientific
Description: 2,4-Dichloro-5-fluorotoluene
UOM: 1 * 2 g


Supplier: Thermo Fisher Scientific
Description: 2,6-Dichloro-4-fluorophenol ≥98%
Catalog Number: (APOSOR27097-1G)
Supplier: Apollo Scientific
Description: 2,6-Dichloro-4-methylnicotinamide
UOM: 1 * 1 g


Catalog Number: (APOSOR309384-1G)
Supplier: Apollo Scientific
Description: 2,6-Dichloro-4-methylquinoline
UOM: 1 * 1 g


Catalog Number: (BOSSBS-12933R-CY3)
Supplier: Bioss
Description: Chymotrypsins are digestive enzymes that can perform proteolysis by cleaving peptides at the carboxyl side of tyrosine, tryptophan, leucine and phenylalanine, although over time they can also hydrolyze other amide bonds, especially those with leucine-donated carboxyls. Chymotrypsins cleave peptide bonds by attacking the non-reactive carbonyl group with a powerful nucleophile, which momentarily becomes covalently bonded to the substrate to form an intermediate. Chymotrypsin B (CTRB1) and Chymotrypsin B2 (CTRB2) are synthesized in the pancreas by protein biosynthesis as precursors that are enzymatically inactive, but become active as three polypeptide molecules that are interconnected by disulfide bonds.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-12933R-CY5)
Supplier: Bioss
Description: Chymotrypsins are digestive enzymes that can perform proteolysis by cleaving peptides at the carboxyl side of tyrosine, tryptophan, leucine and phenylalanine, although over time they can also hydrolyze other amide bonds, especially those with leucine-donated carboxyls. Chymotrypsins cleave peptide bonds by attacking the non-reactive carbonyl group with a powerful nucleophile, which momentarily becomes covalently bonded to the substrate to form an intermediate. Chymotrypsin B (CTRB1) and Chymotrypsin B2 (CTRB2) are synthesized in the pancreas by protein biosynthesis as precursors that are enzymatically inactive, but become active as three polypeptide molecules that are interconnected by disulfide bonds.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-15472R-CY5)
Supplier: Bioss
Description: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-15472R-A350)
Supplier: Bioss
Description: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-15472R-A750)
Supplier: Bioss
Description: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
UOM: 1 * 100 µl


Catalog Number: (H64366.06)
Supplier: Thermo Fisher Scientific
Description: 2,6-Dichloro-3-iodopyridine 98%
UOM: 1 * 5 g

Supplier: Apollo Scientific
Description: Ethyl-4,6-dichloro-5-nitronicotinate

Supplier: Thermo Fisher Scientific
Description: Dichloro(chloromethyl)methylsilane 95%
Supplier: Apollo Scientific
Description: 1,2-Dichloro-2-methylpropane 97%

Supplier: Thermo Fisher Scientific
Description: 2,5-Dichloro-p-phenylenediamine 99%
Catalog Number: (PROOMM0314.03)
Supplier: LGC Standards PROMOCHEM
Description: Organic Standard, Phenylalanine
UOM: 1 * 100 mg


Supplier: Apollo Scientific
Description: 2,6-Dichloro-p-phenylenediamine 98%

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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.
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