carbamoyl


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carbamoyl

 [kahr´bah-moil]
the radical NH2CO–.

car·ba·mo·yl

(kar'bă-mō-il),
The acyl radical, NH2-CO-, the transfer of which plays an important role in certain biochemical reactions, for example, in the urea cycle, via carbamoyl phosphate.

carbamoyl

/car·bam·o·yl/ (kahr-bam´o-il) the radical NH2CO—; see carbamoyltransferase.

car·bam·o·yl

(kahr-bam'ō-ĭl)
The acyl radical, NH2-CO-, the transfer of which plays an important role in certain biochemical reactions.
Synonym(s): carbamyl.

carbamoyl

the radical NH2−CO−.

carbamoyl phosphate synthetases
enzymes catalyzing the synthesis of carbamoyl phosphate. Carbamoyl-phosphate synthetase I is the starting enzyme of the urea cycle. Carbamoyl-phosphate synthetase II is the starting enzyme of pyrimidine synthesis.
References in periodicals archive ?
Carbamoyl chloride and isocyanate dimers will decompose upon injection.
Guarente, "SIRT5 Deacetylates carbamoyl phosphate synthetase 1 and regulates the urea cycle," Cell, vol.
In contrast, the toxin profile of the New Zealand scallop digestive tissues was dominated by carbamoyl toxins, confirming biotransformation of PSP toxin into more toxic compounds.
A colorimetric assay based on the reactivity of carbamoyl groups with diacetylmonoxime may be used (22).
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1,2) This antigen was shown to be carbamoyl phosphate synthetase 1, an enzyme involved in urea synthesis.
With the aid of the allosteric activator N-acetylglutamate synthesized by NAGS, CPS1 catalyzes the transformation of ammonia to carbamoyl phosphate.
4] Human genes: NR0B1 (DAX1), nuclear receptor subfamily 0, group B, member 1; DMD, dystrophin (muscular dystrophy, Duchenne and Becker types); IL1RAPL1, interleukin 1 receptor accessory protein-like 1; GK, glycerol kinase; OTC, ornithine carbamoyl transferase.
Simultaneous separation by high-performance liquid chromatography of carbamoyl aspartate, carbamoyl phosphate and dihydroorotic acid.
New research suggests that low concentrations of citrulline are observed in infants affected with carbamoyl phosphate synthase deficiency and perhaps ornithine transcarbamylase deficiency.