carbamoyl

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carbamoyl

[kär′bam·ə‚wil]
(organic chemistry)
The radical NH2CO, formed from carbamic acid.
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References in periodicals archive ?
sulfamyl and carbamyl groups in the same molecule was achieved in good yield.
Homocitrulline formation following carbamylation of histones with carbamyl phosphate.
Should the carbon to oxygen bond cleave, a carbamyl radical and an alkoxy radical will be formed.
Birds lack carbamyl phosphate synthetase, one of the urea cycle enzymes necessary for the synthesis of citrulline from ornithine in the liver and kidney (Tamir and Ratner, 1963).
MS/MS has proven to be ineffective in reliably identifying deficiencies in the urea-cycle enzymes ornithine transcarbamylase (OTC) and carbamyl phosphate synthetase (CPSI) through the quantitation of citrulline, though is considerably more useful when detecting elevations in this analyte in newborns with a deficiency in argininosuccinic acid synthetase (ASAS) or argininosuccinic acid lyase (ASAL).
3,5,3'-Triiodothyronine-induced carbamyl phosphate synthetase gene expression is stabilized in the liver of Rana catesbeiana tadpoles during heat shock.
The hyperammonemia observed in methylmalonic acidemia is thought to arise because accumulated propionyl CoA interferes with formation of N-acetylglutamate, an obligatory activator of carbamyl phosphate synthase, the initial step in urea synthesis (4).
We are in the process of analyzing various safe, natural plant nutriceutical that may recruit stem cells including low level (S)-nicotine Angiogenix(TM), lobeline, carbamyl, natural choline esterase inhibitors, and others.
Carbamyl phosphate and yeast orotidine-5'phosphate pyrophosphorylase were obtained from Boehringer Mannheim GmbH.
Pearson syndrome or mitochondrial ATP synthase deficiency); Smith-Lemli-Opitz syndrome; carbamyl phosphate synthetase deficiency 3-Methylglutarate As 3-methylglutaconate 4-Hydroxyisovalerate IVA Isovalerylglycine (34) IVA; MAD deficiency; EMA aciduria (short-branched chain acyl-CoA DH deficiency; muscle COX deficiency (c)) Methylcitrate (33, 34, 43) PA; MMA; multiple carboxylase deficiency Methylmalonate MMA; transcobalamine II (27, 34, 43-49) deficiency; malonic aciduria Propionylglycine (33, 34) PA; MMA Tiglylglycine PA; 2-methyl-3-hydroxybutyryl-CoA (30, 31, 33-35, 50) DH deficiency; mitochondrial acetoacetyl-CoA-thiolase deficiency; multiple carboxylase deficiency; respiratory chain defects (e.