acetoacetate การใช้
- Acetoacetate decarboxylase is a 365 kDa complex with a homododecameric structure.
- Beta-diketones appear to inhibit acetoacetate decarboxylase well but slowly.
- Geuther is best known for his discovery of ethyl acetoacetate.
- In alcoholic solution it condenses with sodium acetoacetate to form 4-methylumbelliferone.
- Acetoacetate decarboxylase is inhibited by a number of compounds.
- The smell of acetoacetate and / or acetone in breath is a common feature in ketosis.
- This conversion is one of many steps in breaking L-tyrosine into acetoacetate and fumarate.
- Addition of free cysteine to the inhibited enzyme is able to reverse CMS inhibition of acetoacetate decarboxylase.
- This elevated beta-hydroxybutyrate level is naturally expected, as beta-hydroxybutyrate is formed from acetoacetate.
- Under elevated levels of acetoacetate and D-?-hydroxybutyrate, acetoacetate decarboxylase produces significantly more acetone.
- Under elevated levels of acetoacetate and D-?-hydroxybutyrate, acetoacetate decarboxylase produces significantly more acetone.
- The ketone bodies are possibly anticonvulsant in themselves; in animal models, acetoacetate and acetone protect against seizures.
- Acetoacetate and D-?-hydroxybutyrate freely interconvert through the action of D-?-hydroxybutyrate dehydrogenase.
- The experimental work of his and others yielded puzzling results and induced debates on the nature of ethyl acetoacetate.
- Hantzsch pyridine synthesis with acetoacetate, formaldehyde and ammonium acetate, and iron ( III ) chloride as the catalyst.
- Aldol condensation of acetone and ethyl acetoacetate gave ?-keto-ester "'3 " '.
- Figure 1 : General mechanism of acetoacetate decarboxylase, proceeding through a Schiff base intermediate and producing acetone and carbon dioxide
- Ethyl acetoacetate, a important starting material in organic synthesis, can be prepared using a diketene in reaction with ethanol.
- Thereby fumarate ( also a metabolite of the citric acid cycle ) and acetoacetate ( 3-ketobutyroate ) are liberated.
- Ketone bodies that commonly appear in the urine when fats are burned for energy are acetoacetate and beta-hydroxybutyric acid.
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