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5'D-II 5' deiodinase
5'FSBA 5'-[p-(Fluorosulfonyl)benzoyl]adenosine
5'IAF 5'-(iodoacetamido)-fluorescein
5'MC 5'-methylcytosine
5'Nase 5'-Nucleotidase
5'ND 5' nucleotidase
5'UT 5' Untranslated
5, 6-DHT 5, 6-dihydroxytryptamine
5, 6-EET 5, 6-epoxyeicosatrienoic acid
5,7-3H 4-(3-t- butylamino-2-hydroxypropxy
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5-hydroxyvalerate CoA-transferase <enzyme> Catalyses the formation of 5-hydroxyvaleryl-CoA from 5-hydroxyvalerate and acetyl-CoA; also acts on propionate and 5-hydroxy-2-pentenoate
Registry number: EC 2.8.3.-
(26 Jun 1999)
5-hydroxyvaleryl-CoA dehydratase <enzyme> Contains fad; bifunctional enzyme which catalyses reversible dehydration of 5-hydroxyvaleryl-CoA to 4-pentenoyl-CoA
Registry number: EC 4.2.1.-
Synonym: 5hvc-dehydratase, 5-hydroxyvaleryl-CoA dehydratase-dehydrogenase
(26 Jun 1999)
5-methoxyindole-3-acetate An intermediate of tryptophan and serotonin degradation; excreted as conjugates.
(05 Mar 2000)
5-methoxytryptamine <chemical> 5-methoxy-1h-indole-3-ethanamine. Serotonin derivative proposed as potentiator for hypnotics and sedatives.
Chemical name: 1H-Indole-3-ethanamine, 5-methoxy-
(12 Dec 1998)
5-methylcytosine A minor base that is present in both bacterial and human DNA.
(05 Mar 2000)
5-methylcytosine-DNA glycosylase <enzyme> Binds equally well to methylated and non-methylated DNA; isolated from developing chicken embryos and mouse fibroblasts; mw 52.5 kD
Registry number: EC 3.2.2.-
(26 Jun 1999)
5-methyldeoxycytidine monophosphate aminohydrolase <enzyme> Forms thymidylate; does not act on dcmp
Registry number: EC 3.5.4.-
Synonym: 5mdcmp aminohydrolase
(26 Jun 1999)
5-methylresorcinol 3,5-dihydroxytoluene;the parent substance of the natural dye orcein, obtained from certain colourless lichens (Lecanora tinctoria, Rocella tinctoria) by treatment with boiling water; used as an external antiseptic in various skin diseases and in chemistry as a reagent for pentoses.
Synonym: 5-methylresorcinol, orcin.
(05 Mar 2000)
5-methyltetrahydrofolate-homocysteine s-methyltransferase <enzyme> An enzyme that catalyses the formation of methionine by transfer of a methyl group from 5-methyltetrahydrofolate to homocysteine. It requires a cobamide coenzyme. The enzyme can act on mono- or triglutamate derivatives.
Chemical name: 5-Methyltetrahydropteroyltri-L-glutamate:L-homocysteine S-methyltransferase
Registry number: EC 2.1.1.13
(12 Dec 1998)
5-methylthioribose kinase <enzyme> Forms 5-methylthioribose-1-phosphate
Registry number: EC 2.7.1.100
Synonym: mtr kinase, 5-methylthioadenosine kinase
(26 Jun 1999)
5-NT <biochemistry, enzyme> 5-nucleotidase is a liver enzyme that can be measured in the bloodstream. It can be a specific indicator for liver disease when it is elevated.
The normal value is 0 to 1.6 U/L (units per litre). 5-nucleotidase can be elevated in cholestasis, hepatic ischaemia, liver necrosis, liver tumour, hepatitis and the use of hepatotoxic drugs. The assay is performed on a venipuncture specimen.
Acronym: 5-NT
(19 Jan 1998)
5-nucleotidase <biochemistry, enzyme> 5-nucleotidase is a liver enzyme that can be measured in the bloodstream. It can be a specific indicator for liver disease when it is elevated.
The normal value is 0 to 1.6 U/L (units per litre). 5-nucleotidase can be elevated in cholestasis, hepatic ischaemia, liver necrosis, liver tumour, hepatitis and the use of hepatotoxic drugs. The assay is performed on a venipuncture specimen.
Acronym: 5-NT
(19 Jan 1998)
5-O-(4-coumaroyl)shikimate 3'-hydroxylase <enzyme> Parsley microsomal enzyme; requires NADPH and o2; forms trans-5-o-caffeoylshikimate
Registry number: EC 1.14.13.-
Synonym: cs 3'-hydroxylase
(26 Jun 1999)
5-oxopent-3-ene-1,2,5-tricarboxylate decarboxylase <enzyme> Yields 2-hydroxyhepta-2,4-diene-1,7-dioate; exists as a bifunctional enzyme with 2-hydroxyhepta-2,4-diene-1,7-dioate isomerase in the homoprotocatechuate degradative pathway of E coli
Registry number: EC 4.1.1.68
Synonym: 5-cohed decarboxylase, 5-carboxymethyl-2-oxo-hex-3-ene-1,6-dioate decarboxylase, opet decarboxylase
(26 Jun 1999)
5-oxoprolinase <enzyme> An enzyme that catalyses the ATP-dependent hydrolysis of l-5-oxoproline (ATP + l-5-oxoproline &rarr; ADP + Pi + l-glutamate) a deficiency of this enzyme will result in 5-oxoprolinuria.
(05 Mar 2000)
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A02107073 Dextrose, Potassium Chloride, Sodium Chloride
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A02107054 Dextrose, Potassium Chloride, Sodium Chloride
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A02107063 Dextrose, Potassium Chloride, Sodium Chloride
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5α-r. an enzyme that catalyzes the irreversible reduction of testosterone to dihydrotestosterone with NADPH as the hydrogen donor. Deficiency of the enzyme, with resultant deficiency in dihydrotestosterone, is an autosomal recessive condition characterized by male pseudohermaphroditism, prepubertal ambiguous or female-type external genitalia (usually some form of perineal hypospadias), and some masculinization at puberty without gynecomastia.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
5,10-methenyltetrahydrofolate a substituted derivative of tetrahydrofolate, carrying a methylidyne group; it is formed in histidine degradation and in the interconversion of various folates, linking the flow of activated one-carbon units from serine and thymidylate synthesis with purine synthesis and the liver enzyme system for discarding excess single carbons.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
5,10-methenyltetrahydrofolate synthetase 5-formyltetrahydrofolate cyclo-ligase.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
5,10-methylenetetrahydrofolate a doubly methylated, reduced derivative of folic acid occurring as an intermediate in the transfer of methyl groups to methionine, receiving them from formaldehyde, serine, and glycine.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
5,10-methylenetetrahydrofolate reductase (FADH2) [EC 1.7.99.5] an enzyme of the oxidoreductase class that catalyzes the reduction of 5,10-methylenetetrahydrofolate to 5-methyltetrahdyrofolate, using FADH2 and NADH as primary and secondary electron donors, respectively. The reaction is the means by which methyl groups are generated de novo for methylation reactions. Deficiency of the enzyme, an autosomal recessive trait, results in homocystinuria due to deficiency of 5-methyltetrahydrofolate–homocysteine S-methyltransferase; hypomethioninemia and neurologic abnormalities are present but megaloblastic anemia is absent.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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