Results 301 to 310 of about 90,396 (328)
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Mechanisms of lung tumorigenesis by ethyl carbamate and vinyl carbamate

Drug Metabolism Reviews, 2010
Vinyl carbamate (VC) and ethyl carbamate (EC) induce the formation of lung tumors. The mechanism involves a two-step oxidation of EC to VC and VC to an epoxide, both of which are mediated mainly by CYP2E1. Interaction of the epoxide with DNA leads to the formation of DNA adducts, including 1,N(6)ethenodeoxyadenosine and 1,N(4)-ethenodeoxycytidine.
openaire   +2 more sources

The Pharmacology of Propanediol Carbamates

1971
Publisher Summary This chapter discusses the pharmacology of propanediol carbarnates. The intensive interest generated in the pharmacology of meprobamate represented a departure from previous emphasis on more complex and more sophisticated chemical substances as potential therapeutic agents.
Ludwig Bj, Potterfield
openaire   +3 more sources

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. C. Delbressine   +3 more
openaire   +3 more sources

One-pot conversion of benzyl carbamates into fluorenylmethyl carbamates

Tetrahedron Letters, 2000
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Valerie Dzubeck, Joel P. Schneider
openaire   +3 more sources

Amidation through carbamates

Tetrahedron Letters, 2009
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Latorre, Antonio   +3 more
openaire   +3 more sources

ChemInform Abstract: HYDROGENATION OF N‐ARYL CARBAMATES TO N‐ALICYCLIC CARBAMATES

Chemischer Informationsdienst, 1978
AbstractPhenylcarbaminsäuremethylester (Ia) läßt sich in Isopropanol an 5% Rhodium auf Kohle bei 25 bis 75°C und 35 ‐ 56 bar zu Cyclohexylcarbaminsäure‐methylester (IIa) hydrieren.
Russell E. Malz, Harold Greenfield
openaire   +3 more sources

Toxicology of Organophosphates and Carbamates

1987
Toxicity of a chemical is dependant on several different but interconnected phases: a) factors which influence the delivery of the ultimate toxic agent to its site of action (absorption, distribution, storage, activation, detoxification); b) the reaction with the primary target (reversible or irreversible); c) the biochemical and physiological ...
MORETTO A, JOHNSON MK
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Carbamate Insecticides, Photodecomposition of Carbamate Insecticides

Journal of Agricultural and Food Chemistry, 1965
Ericks Leitis   +2 more
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Cycloserine carbamates

Journal of Medicinal Chemistry, 1974
J D, Weaver, N F, Busch, C H, Stammer
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Preparation of carbamates [PDF]

open access: possiblePharmaceutical Chemistry Journal, 1982
I. A. Kuznetsova   +3 more
openaire   +1 more source

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