Hai cercato: Propyl+acetoacetate

Codice catalogo: (46698-250MG)

Fornitore: Merck

Codice articolo fornitore: 46698-250MG

Codice articolo locale: SUPL46698-250MG

Descrizione: 6-Propyl-2-thiouracil, Supelco®

UOM: 1 * 250 mg

Promo

Codice catalogo: (PRSI25-901)

Fornitore: ProSci Inc.

Codice articolo fornitore: 25-901

Codice articolo locale: PRSI25-901

Descrizione: SLC16A6 is a proton-linked monocarboxylate transporter.It catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate.

UOM: 1 * 50 µG

Promo

Codice catalogo: (8.17036.1000)

Fornitore: Merck

Codice articolo fornitore: 8.17036.1000

Codice articolo locale: MERC8.17036.1000

Descrizione: 6-Propyl-2-thiouracil Ph. Eur.

UOM: 1 * 1 kg

Promo

Fornitore: Merck

Descrizione: Propyl benzoate per sintesi, Sigma-Aldrich®

MSDS

Codice catalogo: (PRSI30-415)

Fornitore: ProSci Inc.

Codice articolo fornitore: 30-415

Codice articolo locale: PRSI30-415

Descrizione: CT1 is a member of the 3-oxoacid CoA-transferase gene family. It is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the reversible transfer of coenzyme A from succinyl-CoA to acetoacetate.This gene encodes a member of the 3-oxoacid CoA-transferase gene family. The encoded protein is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the reversible transfer of coenzyme A from succinyl-CoA to acetoacetate. Mutations in this gene are associated with succinyl CoA:3-oxoacid CoA transferase deficiency.This gene encodes a member of the 3-oxoacid CoA-transferase gene family. The encoded protein is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the reversible transfer of coenzyme A from succinyl-CoA to acetoacetate. Mutations in this gene are associated with succinyl CoA:3-oxoacid CoA transferase deficiency.

UOM: 1 * 50 µG

Promo

Fornitore: Merck

Descrizione: 6-Propyl-2-thiouracil per sintesi, Sigma-Aldrich®

MSDS

Codice catalogo: (PRSI29-925)

Fornitore: ProSci Inc.

Codice articolo fornitore: 29-925

Codice articolo locale: PRSI29-925

Descrizione: SLC16A8 is proton-linked monocarboxylate transporter. It catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate.

UOM: 1 * 100 µG

Promo

Codice catalogo: (PRSI91-973)

Fornitore: ProSci Inc.

Codice articolo fornitore: 91-973

Codice articolo locale: PRSI91-973

Descrizione: 3-Hydroxybutyrate Dehydrogenase Type 2 belongs to the short-chain dehydrogenases/reductases (SDR) family. 3-Hydroxybutyrate Dehydrogenase Type 2 may play an important role in the peripheral utilization of 3-hydroxybutyrate. The cytoplasmic localization with its high ratio of oxidized NAD+, the NAD+ dependence and the kinetic parameters of 3-Hydroxybutyrate Dehydrogenase Type 2 make it suitable to conbert high levels of circulating 3-hydroxybutyrate into acetoacetate.

UOM: 1 * 50 µG

Promo

Codice catalogo: (PRSI91-668)

Fornitore: ProSci Inc.

Codice articolo fornitore: 91-668

Codice articolo locale: PRSI91-668

Descrizione: 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

Promo

Codice catalogo: (PRSI92-016)

Fornitore: ProSci Inc.

Codice articolo fornitore: 92-016

Codice articolo locale: PRSI92-016

Descrizione: 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

Promo

Fornitore: Apollo Scientific

Descrizione: Propyl-2-furancarboxylate 95%

Fornitore: Thermo Fisher Scientific

Descrizione: Propyl chloroformate 98%

MSDS Certificati

Fornitore: TCI

Descrizione: 2-Propyl-2-oxazoline ≥98.0% (by GC)

Fornitore: Thermo Fisher Scientific

Descrizione: n-Propyl bromoacetate 97%

MSDS Certificati

Codice catalogo: (APOSOR930774-100G)

Fornitore: Apollo Scientific

Codice articolo fornitore: OR930774-100G

Codice articolo locale: APOSOR930774-100G

Descrizione: Propyl cyanoacetate 95%

UOM: 1 * 100 g

Promo

Fornitore: Apollo Scientific

Descrizione: n-Propyl carbamate 95%