Results 141 to 150 of about 810 (205)
ChemMedChem, Volume 21, Issue 16, 27 August 2026.Can an amide analog retain the high potency of the classic urea motif in soluble epoxide hydrolase inhibitors? Through a single unconventional switch, the introduction of the underexplored pentafluorosulfanyl group into an amide analog of TPPU, the authors restored high inhibitory potency.
Alba López‐Ruiz +17 more
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ChemMedChem, Volume 21, Issue 16, 27 August 2026.Five novel series of isatin–Schiff base derivatives are synthesized and evaluated for neuroprotective and anti‐infective potential. The compounds demonstrate exceptional, reversible, and competitive monoamine oxidase inhibition, with chloro‐substitutions dictating isoform selectivity.
Marthinus J. Jooste +4 more
wiley +1 more source
Advanced Synthesis &Catalysis, Volume 368, Issue 16, 18 August 2026.A Strecker‐type reaction of aromatic ortho‐diamines with various aldehydes and cyanide assembles the bicyclic amidine core of flavin‐derived heterocycles under mild conditions. Subsequent oxidation, radical or photochemical cyanation, carboxylation with CO2, and CO2‐mediated cyclization build the three‐ring alloxazine scaffold. This sequence provides a
Christian Held +2 more
wiley +1 more source
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Chromatographic Reviews, 1967
Abstract We have attempted to stress the major areas of chromatographic techniques for carbamate analyses and also to illustrate the influence of carbamate moiety substituents on chromatographic behavior. The remarkable versatility of chromatographic techniques, as demonstrated by their many applications to complex analyses, is apparent from the ...
L, Fishbein, W L, Zielinski
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Abstract We have attempted to stress the major areas of chromatographic techniques for carbamate analyses and also to illustrate the influence of carbamate moiety substituents on chromatographic behavior. The remarkable versatility of chromatographic techniques, as demonstrated by their many applications to complex analyses, is apparent from the ...
L, Fishbein, W L, Zielinski
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A method for the determination of methyl carbamate and ethyl carbamate in wines
Food Additives and Contaminants, 1992A method is described for the simultaneous determination of methyl carbamate (MC) and ethyl carbamate (EC) in wines that is based on: (a) extraction of the sample with dichloromethane using an extraction tube or an alumina-Celite column, (b) concentration of the extract to a small volume, and (c) determination by gas-liquid chromatography-thermal ...
N P, Sen, S W, Seaman, D, Weber
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POISONING BY CARBAMATE PESTICIDES
Medical Journal of Australia, 1977In recent years the number of carbamate pesticides registered for use in New South Wales has increased. Some of the newer carbamates are very toxic and have cholinergic properties similar to those of the organic phosphates, though the effect is of much shorter duration.
G R, Simpson, S, Bermingham
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On the formation of carbamate glucuronides
Xenobiotica, 1990(1990). On the formation of carbamate glucuronides. Xenobiotica: Vol. 20, No. 1, pp. 133-134.
L P, Delbressine +3 more
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The basis of the carbamate reaction
Archives of Biochemistry and Biophysics, 1955Abstract Previously, it had been assumed that the carbamination of amino acids could be carried out only in strongly alkaline media (in the presence of alkaline-earth hydroxides). The carbamino carboxylic acids, however, are also formed at neutral and mildly acid reactions.
C, NEUBERG, A, GRAUER, M, KREIDL
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The Metabolism Of Pesticidal Carbamates
CRC Critical Reviews in Toxicology, 1971(1971). The Metabolism Of Pesticidal Carbamates. CRC Critical Reviews in Toxicology: Vol. 1, No. 1, pp. 33-54.
A. J. Ryan, James B. Knaak
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