carbamoyl


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carbamoyl

[kär′bam·ə‚wil]
(organic chemistry)
The radical NH2CO, formed from carbamic acid.
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1995) studied the expression of the enzymes involved in the enterocytes of birds (P-5-C synthetase, ornithine aminotransferase, and ornithine carbamoyltransferase), besides carbamoyl phosphatase synthetase, which gives the compound carbamoyl phosphate.
It is tied up as carbamoyl chloride or captured by free amines as hydrochloride salts.
In the urea cycle, Citn is produced from ornithine and carbamoyl phosphate.
The main target of Sirt5 in the mitochondria is the urea cycle enzyme carbamoyl phosphate synthetase 1 (CPS-1) [18].
Dimethoate (DM) [O,O-dimethyl S-methyl carbamoyl phosphorodithioate] is one of the most important organophosphorus insecticide used extensively on a large number of crops against several pests [1].
Transformation of paralytic shellfish toxins occurs after consumption of dinoflagellates by bivalve species, and research suggests that the bivalves usually have lower proportions of N-sulfocarbomyl toxins and higher proportions of carbamoyl toxins than the toxigenic dinoflagellates that were ingested (Oshima et al.
The following drugs were used: carbamoyl choline (carbachol), norepinephrine (NE), [N.
This is in contrast to the inhibition of 11[beta]-HSD2 by dithiocarbamates, which irreversibly inhibit the enzyme, probably through covalent modification of a cysteine residue by attachment of a carbamoyl group (Atanasov et al.
5 CM,Super - absorbant , polyurethane foam dressing with Vertical Absorption with Silicon Wound Contact Layer Heel 2D 16X24,Super - absorbant , Bacteria Binding polyurethane foam dressing with Dialkyl Carbamoyl Chloride layered 12.
Hepatocyte paraffin antigen 1 (Hep Par 1), which recognizes the urea cycle enzyme carbamoyl phosphate synthetase, (1) and polyclonal antibody directed against carcinoembryonic antigen (pCEA) are among the most commonly used hepatocellular markers, but they have less than 50% sensitivity for poorly differentiated HCC.
2]) is a powerful reagent allowing in an effective way access to key reactives such as ehloroformates, acid chlorides and carbamoyl chlorides, thereby permitting the clean and efficient construction of isocyanates, carbonates, carbamides or ureas.