| sarcosine | <chemical> An amino acid occurring as an intermediate in the metabolism of choline in the kidney and liver. It is normally not detectable in human blood or urine. Chemical name: Glycine, N-methyl- (12 Dec 1998) |
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| sarcosine dehydrogenase | <enzyme> An enzyme that cleaves sarcosine using some acceptor to produce glycine, formaldehyde, and a reduced acceptor molecule; a deficiency of this enzyme will result in sarcosinaemia. (05 Mar 2000) |
| sarcosine oxidase | <enzyme> Catalyses the oxidative demethylation of sarcosine to glycine Registry number: EC 1.5.3.1 Synonym: sarcosine-oxygen oxidoreductase (demethylating) (26 Jun 1999) |
| sarcosine reductase | <enzyme> Involved in sarcosine metabolism in eubacterium acidaminophilum Registry number: EC 1.4.4.- Synonym: n-methylglycine reductase (26 Jun 1999) |
| 1-sarcosine-8-isoleucine angiotensin II | <chemical> An angiotensin II analog which acts as a highly specific inhibitor of angiotensin II. Pharmacological action: angiotensin-converting enzyme inhibitors, antihypertensive agents. Chemical name: Angiotensin II, 1-(N-methylglycine)-8-L-isoleucine- (12 Dec 1998) |
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Synonyms : Magnesium Sarcosylate, N-Methylglycine, Sarcosine Hydrochloride, Sarcosine Monosodium Salt, Sodium Sarcosinate, N Methylglycine, Sarcosinate, Sodium, Sarcosylate, Magnesium
Synonyms : Monomethylglycine Dehydrogenase, Sarcosine N-Demethylase, Dehydrogenase, Monomethylglycine, Dehydrogenase, Sarcosine, N-Demethylase, Sarcosine, Sarcosine N Demethylase
Synonyms : L-Pipecolic Acid Oxidase, Sarcosine-Oxygen Oxidoreductase (Demethylating), Acid Oxidase, L-Pipecolic, L Pipecolic Acid Oxidase, Oxidase, L-Pipecolic Acid, Oxidase, Sarcosine
| sarcosine |
a sweetish crystalline amino acid
출처: wordnet.princeton.edu/perl/webwn
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| sarcosine |
Sarcosine is formed through the decomposition of creatine.
출처: www.always-youthful.com/definitions/s.shtml
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| sarcosine dehydrogenase |
[EC 1.5.99.1] a mitochondrial enzyme of the oxidoreductase class that catalyzes the oxidative demethylation of sarcosine to form glycine; electrons are transferred via its flavin (FAD) cofactor to electron transfer flavoprotein. Folate is also a cofactor. The reaction occurs in the inner mitochondrial membrane in liver and kidney; deficiency of the enzyme, an autosomal recessive trait, results in sarcosinemia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| sarcosinemia |
1. an autosomal recessive aminoacidopathy caused by deficiency of sarcosine dehydrogenase and characterized by accumulation and excretion of sarcosine; it is probably benign but may be associated with neurologic abnormalities. 2. accumulation of sarcosine in the blood, usually resulting from defects in sarcosine dehydrogenase or electron transfer flavoprotein, or from severe folate deficiency. Called also hypersarcosinemia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| sarcosine | a sweetish crystalline amino acid |
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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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