Results 181 to 190 of about 4,043 (236)
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Pharmacokinetics and pharmacodynamics of valproate analogs in rats. II. Pharmacokinetics of octanoic acid, cyclohexanecarboxylic acid, and 1‐methyl‐1‐cyclohexanecarboxylic acid

Biopharmaceutics & Drug Disposition, 1993
AbstractThe pharmacokinetics of valproic acid (VPA) and three structural analogs, octanoic acid (OA), cyclohexanecarboxylic acid (CCA), and 1‐methyl‐1‐cyclohexanecarboxylic acid (MCCA), were examined in female Sprague‐Dawley rats. All four carboxylic acids evidenced dose‐dependent disposition.
M J, Liu, G M, Pollack
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Oxidative decarboxylation of cyclohexanecarboxylic acid

Recueil des Travaux Chimiques des Pays-Bas, 1963
AbstractCyclohexanecarboxylic acid is converted to a mixture of cyclohexanone and cyclohexene by reacting it at temperatures around 200° with an oxygen‐containing gas and steam in the presence of metal‐salt catalysts.
J. A. Bigot, P. L. Kerkhoffs
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Origin of cyclohexanecarboxylic acid in Bacillus acidocaldarius

Phytochemistry, 1974
Abstract In Bacillus acidocaldarius , shikimic acid is converted into the cyclohexancearboxylic acid precursor of fatty acids by way of cyclohexene-l-carboxylic acid, but not by way of cyclohexene-3- or -4-carboxylic acid or benzoic acid.
Mario de Rosaau   +2 more
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ChemInform Abstract: Cyclohexanecarboxylic Acid Derivatives from Psiadia trinervia.

ChemInform, 1992
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.
Y. WANG   +3 more
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ChemInform Abstract: MIXED ANHYDRIDES OF CYCLOHEXANECARBOXYLIC ACID WITH SULPHONIC ACIDS

Chemischer Informationsdienst, 1974
AbstractDas durch Pyrolyse von Cyclohexancarbonsäureanhydrid erhaltene" Pentamethylenketen (I) reagiert mit den Sulfonsäuren (II) zu den gemischten Anhydriden (III), die als Acylierungsmittel geeignet sind, wie am Beispiel ihrer Umsetzung mit β‐Naphthol zu dem Ester (IV) (98, 91 bzw. 89% Ausbeute) bewiesen wird.
EZIO TEMPESTI   +4 more
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Spirocyclic Dipeptides of 1-Amino-1-cyclohexanecarboxylic Acid

Collection of Czechoslovak Chemical Communications, 1994
Spirocyclic cyclodipeptides with 1-amino-1-cyclohexanecarboxylic acid of the general formula cyclo(-Ach-A-), where A is Gly, L-Ala, D-Ala, L-Val, D-Val, L-Leu, D-Leu, D-Pgl, L-Phe or D-Phe, have been prepared by cyclization of the corresponding linear dipeptide methyl esters.
Jarmila Vinšová   +2 more
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Pharmacokinetics and Pharmacodynamics of Valproate Analogues in Rats. IV. Anticonvulsant Action and Neurotoxocity of Octanoic Acid, Cyclohexanecarboxylic Acid, and 1‐Methyl‐1 ‐Cyclohexanecarboxylic Acid

Epilepsia, 1994
Summary: We examined the pharmacodynamics of valproate (VPA) and three structural analogues, octanoic acid (OA), cyclohexanecarboxylic acid (CCA), and 1‐methyl‐1‐cyclohexanecarboxylic acid (MCCA) in rats. A pentylenetetrazol (PTZ) infusion seizure model was used to determine threshold convulsive doses of PTZ; the increase in PTZ threshold dose after ...
M J, Liu, G M, Pollack
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The metabolism of cyclohexanecarboxylic acid and 3-cyclohexenecarboxylic acid by Pseudomonas putida

Canadian Journal of Microbiology, 1982
A strain of Pseudomonas putida grew rapidly on cyclohexanecarboxylic acid as a sole source of carbon. A CoA-mediated β-oxidation pathway was induced for the metabolism of the compound. The organism could not utilize 3-cyclohexenecarboxylic acid as a sole source of carbon for growth, but cells grown on gluconate in the presence of 3 ...
Blakley, E. R., Papish, B.
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A cyclohexanecarboxylic acid utilizing yeast: isolation, identification, and nutritional characteristics

Canadian Journal of Microbiology, 1982
A yeast capable of utilizing cyclohexanecarboxylic acid as sole carbon and energy source, strain KUY-6A, was isolated from soil by enrichment cultures. Taxonomical studies indicated that strain KUY-6A was Trichosporon cutaneum. Strain KUY-6A grew on a number of carboxylic acids.
Yoshie Hasegawa   +4 more
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The metabolism of cyclohexanecarboxylic acid in phaseolus vulgaris

Phytochemistry, 1970
Abstract Cyclohexanecarboxylic acid is converted to 1-cyclohexanecarbonyl-β- d -glucose and N -cyclohexanecarbonyl- l -aspartic acid when administered to leaf disks of Phaseolus vulgaris in the light.
J.G. Severson, B.A. Bohm, C.E. Seaforth
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