| Prodan | 6-propionyl-2-(dimethylamino)-naphthalene |
|---|---|
| LPC | L-Propionyl carnitine |
| PCC | Propionyl CoA carboxylase |
| PLC | Propionyl L-carnitine |
| propionyl | <chemistry> The hypothetical radical C3H5O, regarded as the essential residue of propionic acid and certain related compounds. Source: Websters Dictionary (01 Mar 1998) |
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| propionyl CoA hydrolase | <enzyme> Nadh sensitive; found in brown adipose tissue mitochondria of rat; prevents a deterimental increase of propionyl-CoA in mitochondria; mw at least 240 kD Registry number: EC 3.1.2.- Synonym: propionyl coenzyme a hydrolase (26 Jun 1999) |
| propionyl-CoA | The coenzyme A thioester derivative of propionic acid; an intermediate in the degradation of l-valine, l-isoleucine, l-threonine, l-methionine, and odd-chain fatty acids; a precursor for the synthesis of odd-chain fatty acids; it accumulates in individuals with a deficiency of propionyl-CoA carboxylase. Propionyl-CoA carboxylase, an enzyme that catalyses the reaction of propionyl-CoA with CO2 and ATP to produce ADP, inorganic phosphate, and d-methylmalonyl-CoA; a biotin-dependent enzyme; an inherited deficiency of this enzyme will lead to propionic acidemia and developmental retardation. (05 Mar 2000) |
| propionyl-CoA carboxylase | <enzyme> See also propionyl CoA carboxylase (ATP-hydrolyzing) (EC 6.4.1.4) Registry number: EC 4.1.1.41 Synonym: methylmalonyl-CoA decarboxylase, propionyl-coenzyme a carboxylase (26 Jun 1999) |
| propionylcholinesterase | <enzyme> Aspect of cholinesterase EC 3.1.1.8 Registry number: EC 3.1.1.- (26 Jun 1999) |
| propionylglycine | CH3CH2CONHCH2COOH;a minor metabolite that accumulates in individuals with propionic acidemia. (05 Mar 2000) |
| propionyl |
the acyl radical of propionic acid; the thioester it forms with coenzyme A, propionyl CoA, is an intermediate in the degradation of some amino acids and in the oxidation of odd number chain length fatty acids.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| propionyl-CoA carboxylase |
[EC 6.4.1.3] an enzyme of the ligase class that catalyzes the carboxylation of propionyl CoA to form methylmalonyl CoA; the reaction is part of the route by which three-carbon compounds from some amino acids and from odd numbered fatty acids are used as fuels. The enzyme is an oligomer comprising 4α and 4β chains and requires a biotin cofactor. Deficiency of enzyme activity due to a defect in either chain, an autosomal recessive trait, causes propionicacidemia; see also multiple carboxylase deficiency, under carboxylase.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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