You Searched For: Dimethyl+fumarate

Catalog Number: (PROOMM1329.00)

Supplier: LGC Standards PROMOCHEM

Description: Organic Standard, Tenofovir disoproxil fumarate

UOM: 1 * 100 mg

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Catalog Number: (PROOLGCFOR0394.00)

Supplier: LGC Standards PROMOCHEM

Description: Organic Standard, Tiamulin hydrogen fumarate

UOM: 1 * 10 mg

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Catalog Number: (EDQMY0000333)

Supplier: EDQM

Description: Organic Standard, Tiamulin hydrogen fumarate, Pack type: Vial

UOM: 1 * 500 mg

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Supplier: LGC Standards PROMOCHEM

Description: Organic Standard, 3-ethyl 5-methyl 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-6-methylpyridine-3,5-dicarboxylate fumarate

Catalog Number: (EDQMY0001657)

Supplier: EDQM

Description: Organic Standard, Quetiapine fumarate

UOM: 1 * 50 mg

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Catalog Number: (PROOMM0386.12)

Supplier: LGC Standards PROMOCHEM

Description: Organic Standard, 3-Ethyl 5-methyl 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-6-methylpyridine-3,5-dicarboxylate fumarate

UOM: 1 * 100 mg

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Supplier: Thermo Fisher Scientific

Description: Thiabendazole, a metal chelator and helminth-specific fumarate reductase inhibitor, is used primarily as an anthelmintic to control infections by helminth organisms.

MSDS Certificates

Catalog Number: (PRSI91-668)

Supplier: ProSci Inc.

Description: Fumarylacetoacetase belongs to the FAH family. Fumarylacetoacetase is primary expressed in liver and kidney. It exists as a homodimer and catalyses the hydrolysis of 4-fumarylacetoacetate into fumarate and acetoacetate. Defects in Fumarylacetoacetase cause tyrosinemia type 1, which is congenital metabolism defect characterised by elevated levels of tyrosine in the blood and urine, and hepatorenal manifestations. Typical features include renal tubular injury, self-mutilation, hepatic necrosis, episodic weakness, and seizures.

UOM: 1 * 50 µG

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Supplier: MP Biomedicals

Description: Succinic acid is a dicarboxylic acid that occurs in nature in such organisms as fungi and lichens. In eukaryotes, succiniate, the anion of succinic acid, is an intermediate in the citric acid cycle, being formed from succinyl CoA and being converted to fumarate. Bacteria and plants can produce succinate from acetate or acetyl CoA, in the glyoxylate cycle.

Catalog Number: (PRSI91-204)

Supplier: ProSci Inc.

Description: Fumarase is an enzyme that catalyze the reversible hydration/dehydration of fumarate to S-malate and is involved in the tricarboxylic acid or Krebs cycle. Fumarase exists in both form, cytosolic formand N-terminal extend mitochondrial form. The N-terminal extended form is targeted to the mitochondrion, where the removal of the extension is the same form as in the cytoplasm. Fumarase is thought to act as a tumour suppressor, which deficiency can lead to progressive encephalopathy, cerebral atrophy and development delay.

UOM: 1 * 50 µG

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Catalog Number: (PRSI29-614)

Supplier: ProSci Inc.

Description: ASL is a member of the lyase 1 family. The protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in its gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency.This gene encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described.

UOM: 1 * 50 µG

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Catalog Number: (PRSI29-615)

Supplier: ProSci Inc.

Description: ASL is a member of the lyase 1 family. The protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in its gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency.This gene encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described.

UOM: 1 * 100 µG

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Catalog Number: (PRSI92-016)

Supplier: ProSci Inc.

Description: 4-Hydroxyphenylpyruvate Dioxygenase (4HPPD) belongs to the 4HPPD family. 4HPPD is a key enzyme in the degradation of tyrosine, which catalyzes the second reaction in the catabolism of tyrosine the conversation of 4-hydroxyphenylpyruvate to homogentisate. 4HPPD exists in homodimer forms, which uses zinc as a cofactor to catalyze the third step in the conversion of L-phenylalanine to fumarate and acetoacetic acid. When the active 4HPPD enzyme concentration is low in the human body, it results in high levels of tyrosine concentration in the blood, which can cause mild mental retardation at birth, and degradation in vision as a patient grows older.

UOM: 1 * 50 µG

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Supplier: Merck

Description: (+)-Dimethyl-D-malate for synthesis

Supplier: Merck

Description: Dimethyl succinate for synthesis, Sigma-Aldrich®

Supplier: SIGMA ALDRICH MICROSCOPY

Description: N,N-Dimethyl-1-naphthylamine is an aromatic amine and a dye.