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Relevant bibliographies by topics / Dicarboxylic

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Academic literature on the topic 'Dicarboxylic'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Dicarboxylic"

1

Vamecq, J., E. de Hoffmann, and F. Van Hoof. "The microsomal dicarboxylyl-CoA synthetase." Biochemical Journal 230, no. 3 (1985): 683–93. http://dx.doi.org/10.1042/bj2300683.

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Dicarboxylic acids are products of the omega-oxidation of monocarboxylic acids. We demonstrate that in rat liver dicarboxylic acids (C5-C16) can be converted into their CoA esters by a dicarboxylyl-CoA synthetase. During this activation ATP, which cannot be replaced by GTP, is converted into AMP and PPi, both acting as feedback inhibitors of the reaction. Thermolabile at 37 degrees C, and optimally active at pH 6.5, dicarboxylyl-CoA synthetase displays the highest activity on dodecanedioic acid (2 micromol/min per g of liver). Cell-fractionation studies indicate that this enzyme belongs to the

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Vamecq, J., J. P. Draye, and J. Brison. "Rat liver metabolism of dicarboxylic acids." American Journal of Physiology-Gastrointestinal and Liver Physiology 256, no. 4 (1989): G680—G688. http://dx.doi.org/10.1152/ajpgi.1989.256.4.g680.

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Recently, we demonstrated in rat liver that dicarboxylic acids containing more than five carbons can be activated by a microsomal dicarboxylyl-CoA synthetase (J. Vamecq, E. de Hoffmann, and F. Van Hoof. Biochem. J. 230: 683-693, 1985). The products of this reaction, dicarboxylyl-CoA esters, were found to be substrates for an H2O2-generating dicarboxylyl-CoA oxidase. In the present work we report that 1) the catalytic center or the essential domains of dicarboxylyl-CoA synthetase are located at the cytosolic aspect of the endoplasmic reticulum membrane; 2) dicarboxylyl-CoA oxidase is optimally

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3

Stephanou, E. G. "?,?-Dicarboxylic acid salts and?,?-dicarboxylic acids." Naturwissenschaften 79, no. 3 (1992): 128–31. http://dx.doi.org/10.1007/bf01131541.

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4

Tonsgard, J. H., and S. C. Meredith. "Characterization of the binding sites for dicarboxylic acids on bovine serum albumin." Biochemical Journal 276, no. 3 (1991): 569–75. http://dx.doi.org/10.1042/bj2760569.

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Dicarboxylic acids are prominent features of several diseases, including Reye's syndrome and inborn errors of mitochondrial and peroxisomal fatty acid oxidation. Moreover, dicarboxylic acids are potentially toxic to cellular processes. Previous studies [Tonsgard, Mendelson & Meredith (1988) J. Clin. Invest. 82, 1567-1573] demonstrated that long-chain dicarboxylic acids have a single high-affinity binding site and between one and three lower-affinity sites on albumin. Medium-chain-length dicarboxylic acids have a single low-affinity site. We further characterized dicarboxylic acid binding t

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5

Kamoun, P., Ph Parvy, D. Rabier, J. Bardet, T. Billette de Villemeur, and J. M. Saudubray. "Dicarboxylic aminoaciduria." Journal of Inherited Metabolic Disease 17, no. 6 (1994): 758. http://dx.doi.org/10.1007/bf00712024.

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6

Kropacheva, Polina P., Larisa G. Kubarskaya, and Mariia A. Brusina. "Bis-methylamides of 1,2-dialkyl substituted imidazole-4,5-dicarboxylic acids: preparation and antinociceptive activity." Medical academic journal 24, no. 3 (2024): 87–94. https://doi.org/10.17816/maj630226.

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BACKGROUND: Searching for substances with high analgesic activity is one of the main problems of modern medicine. N-methyl-D-aspartate receptors present in all areas of the central nervous system responsible for reaction on pain stimulation. Moreover, peripheral glutamate receptors may be directly involved in the genesis of pain reactions. Therefore, it is of interest to search for new analgesics among N-methyl-D-aspartate receptor ligands. AIM: To develop a preparative method of synthesis and to investigate the antinociceptive activity of 1,2-dialkylimidazole-4,5-dicarboxylic acids bis-methyl

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7

Modrzakowski, Malcolm C., and William R. Finnerty. "Intermediary metabolism of Acinetobacter grown on dialkyl ethers." Canadian Journal of Microbiology 35, no. 11 (1989): 1031–36. http://dx.doi.org/10.1139/m89-171.

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The microbial dissimilation of long-chain dialkyl ethers by Acinetobacter sp. H01-N involved a terminal methyl group oxidation of the dialkyl ether substrates, resulting in the formation of ether oxygen containing fatty acids of corresponding chain length. An internal carbon–carbon scission of the dialkyl ethers resulted in the formation of end-product ether fatty acids and corresponding dicarboxylic acids. Cellular carbon and energy were derived from the subsequent metabolism of the dicarboxylic acids. Dicarboxylic acid oxidation, activation, and identification of cellular dicarboxylic acids

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8

Ranea-Robles, Pablo, and Sander M. Houten. "The biochemistry and physiology of long-chain dicarboxylic acid metabolism." Biochemical Journal 480, no. 9 (2023): 607–27. http://dx.doi.org/10.1042/bcj20230041.

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Mitochondrial β-oxidation is the most prominent pathway for fatty acid oxidation but alternative oxidative metabolism exists. Fatty acid ω-oxidation is one of these pathways and forms dicarboxylic acids as products. These dicarboxylic acids are metabolized through peroxisomal β-oxidation representing an alternative pathway, which could potentially limit the toxic effects of fatty acid accumulation. Although dicarboxylic acid metabolism is highly active in liver and kidney, its role in physiology has not been explored in depth. In this review, we summarize the biochemical mechanism of the forma

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RAJINDER, PARSHAD, and S. SHARMA K. "Photolysis of Substituted Benzylidineacenaphthenones." Journal Of Indian Chemical Society Vol. 66, Feb 1989 (1989): 106–9. https://doi.org/10.5281/zenodo.6302322.

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Department of Chemistry, M. D. University, Rohtak 124 001 <em>Manuscript received 7 March 1988, revised 27 September 1988, accepted 4 October 1988</em> Substituted benzylidineacenaphthenones were photolysed In benzene in presence of air.  Cyclodehydrogenation led to substituted-benzochrysenes as well as photo-oxidative cleavage of benzylidine double bond leading to Papbthalene-1,8-dicarboxylic acid anhydride as the major product Photolysis of acuaphthenone also gave naphthalene-1,8-dicarboxyli acid anhydride under the same condition In which the ben

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10

Elix, JA, R. Naidu, and JR Laundon. "A Synthesis of the Lichen Dibenzofuran Pannaric Acid 2-Methyl Ester and Its Isomer 3-O-Methylpannaric Acid." Australian Journal of Chemistry 45, no. 4 (1992): 785. http://dx.doi.org/10.1071/ch9920785.

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A total synthesis of pannaric acid 2-methyl ester (2-methyl hydrogen 3,9-dihydroxy-1,7-dimethyldibenzofuran-2,6-dicarboxylae) (1) and 3-O-methylpannaric acid (9-hydroxy- 3-methoxy-1,7-dimethyldibemofuran-2,6-dicarboxylic acid) (2) has been achieved through a biomimetic-type approach by using palladium(n) acetate in the key cyclization step. The acid (1) was shown to be identical to a major metabolite of the lichen Roccella capensis and a minor or trace constituent of the lichens Leproloma diffusum and L. vouauxii.

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Dissertations / Theses on the topic "Dicarboxylic"

1

Etuwewe-Mordi, Oritsejolomi Elsie. "Dicarboxylic acids in the environment." Thesis, University of Liverpool, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.539602.

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Yu, Sze-chit. "Syntheses and physical properties of polymers based on 2,2'-bipyridine dicarboxylic acid and pyridine-2,6-dicarboxylic acid /." Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B20978650.

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Saayman, Maryna. "Characterisation of the malate transporter and malic enzyme from Candida utilis." Thesis, Stellenbosch : University of Stellenbosch, 2011. http://hdl.handle.net/10019.1/16520.

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Dissertation (PhD)--University of Stellenbosch, 2005.<br>ENGLISH ABSTRACT: Yeast species differ remarkably in their ability to degrade extracellular dicarboxylic acids and to utilise them as their only source of carbon. The fission yeast Schizosaccharomyces pombe effectively degrades L-malate, but only in the presence of an assimilable carbon source. In contrast, the yeast Saccharomyces cerevisiae is unable to effectively degrade L-malate, which is ascribed to the slow uptake of L-malate by diffusion. In contrast, the yeast Candida utilis can utilise L-malate as the only source of carbon

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Komba, Christele Lydia. "Chiral discrimination of dicarboxylic acids with Cinchona alkaloids." Thesis, Cape Peninsula University of Technology, 2017. http://hdl.handle.net/20.500.11838/2571.

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Thesis (MTech (Chemistry))--Cape Peninsula University of Technology, 2017.<br>This thesis is aimed at the investigation of the chiral discrimination process during diastereomeric salt formation, when selected cinchona alkaloids are exposed to racemic mixtures of tartaric acid derivatives. This research is based on the use of (+)‐cinchonine, (‐)‐cinchonidine, (‐)‐quinidine and (+)‐ quinine, which served as chiral bases, in order to resolve racemates of O,O'‐dibenzoyl‐tartaric acid (DBTA) and O,O'‐di‐p‐toluoyl‐tartaric acid (DTTA). Cinchona alkaloids were selected because of their abilities

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Kimura, Hidenori. "Development of Axially Chiral Dicarboxylic Acid-Catalyzed Asymmetric Transformations." 京都大学 (Kyoto University), 2012. http://hdl.handle.net/2433/157841.

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Williams, Richard Charles. "Routes to heterocyclic prostanoids from allene-1,3-dicarboxylic esters." Thesis, University of Salford, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.258229.

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Rambocus, Subhas. "Reactive solvent extraction of dicarboxylic and carboxylic-sulfonic acids." Thesis, London South Bank University, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.245144.

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Breitkopf, Ronja. "Understanding the C4 dicarboxylic acid metabolism in Clostridium autoethanogenum." Thesis, University of Nottingham, 2018. http://eprints.nottingham.ac.uk/49588/.

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The acetogenic bacterium Clostridium autoethanogenum possesses the inherent ability to produce acetate and ethanol during growth on industrial waste gases such as carbon monoxide and carbon dioxide using the Wood-Ljungdahl Pathway (WLP) for carbon fixation. With the urgent need to reduce greenhouse gas emissions and produce chemicals and fuels in a more sustainable manner, autotrophic organisms such as C. autoethanogenum have received considerable industrial interest over recent years. However, the metabolic pathways present in C. autoethanogenum and therefore its capability to produce industr

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9

Broadway, Neil Michael. "Enzymology of dicarboxylic acid metabolism in Corynebacterium sp. strain 7E1C." Thesis, University of Hull, 1990. http://hydra.hull.ac.uk/resources/hull:3741.

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1.Dicarboxylic acid metabolism was investigated in the alkane-utilizing bacterium Corynebacterium 7E1C.2.The best yields of dicarboxylic acid were obtained during growth on dodecane although significant amounts of tetradecanedioic acid were produced during growth on methyl myristate. No dicarboxylic acid was produced during growth on hexadecane, methyl palmitate or 16-hydroxypalmitate.3.Corynebacterium 7E1C possesses constitutive NAD+-dependent and NADP+-dependent alcohol dehydrogenases active with mono-ol, a, w-diol and (L)-hydroxyfatty acids. Additional NADP+-dependent octanol dehydrogenase

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Thompson, Alison Jane. "Substrate enhanced asymmetric synthesis of the 1-aminocyclopentane-1,3-dicarboxylic acids." Thesis, University of Oxford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299760.

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Books on the topic "Dicarboxylic"

1

Williams, Richard Charles. Routes to heterocyclic prostanoids from Allene-1,3-dicarboxylic esters. University of Salford, 1989.

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2

J, Rotberg, and United States. National Aeronautics and Space Administration, eds. Dicarboxylic acid anhydride condensation with compounds containing active methylene groups. National Aeronautics and Space Administration, 1985.

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3

P, Oshkaya V., and United States. National Aeronautics and Space Administration., eds. Condensation af anhydrides of dicarboxylic acids with compounds containing active methylene groups. National Aeronautics and Space Administration, 1985.

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4

Devor, Arthur William. Oxidation of Monosaccharoses and Their Monomethyl Derivatives to Dicarboxylic Acids. Creative Media Partners, LLC, 2021.

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5

Condensation of anhydrides of dicarboxylic acids with compounds containing active methylene groups. National Aeronautics and Space Administration, 1985.

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6

Bearne, Stephen Lewis *. Enzyme inhibition by phosphonates and protein modification by dicarboxylic acid bis (methyl phosphates). 1991.

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7

(Editor), H. U. Bergmeyer, J. Bermeyer (Editor), and M. Bral (Editor), eds. Methods of Enzymatic Analysis, 3.eE, Vol. 7, Metabolites 2: Tri- and Dicarboxylic Acids, Purines, Pyrimidines and Derivatives, Coenzymes, Inorganic Compounds. 3rd ed. John Wiley & Sons, 1985.

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8

Tübingen, Universität, ed. Regulation des Natrium-Dicarboxylat Kotransporters durch Serum- und Glukokortikoid-abhängige Kinasen und Proteinkinase B. 2007.

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Book chapters on the topic "Dicarboxylic"

1

Gooch, Jan W. "Dicarboxylic Acid." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3542.

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2

Cleaves, Henderson James. "Dicarboxylic Acid." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_427.

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Cleaves, Henderson James. "Dicarboxylic Acid." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_427.

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Cleaves, Henderson James. "Dicarboxylic Acid." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65093-6_427.

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Cleaves, Henderson James. "Dicarboxylic Acid." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-642-27833-4_427-5.

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6

Metze, Dieter, Tam Nguyen, Birgit Haack, et al. "Dicarboxylic Aminoaciduria." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_484.

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Cleaves, Henderson James. "Dicarboxylic Acid." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27833-4_427-4.

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Pollex, Rolf, Edwin Weber, and Mátyás Czugler. "Preorganized Macrocyclic Dicarboxylic Receptors." In Molecular Recognition and Inclusion. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5288-4_85.

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9

Holze, Rudolf. "Ionic conductance of 1,1-cyclopentane dicarboxylic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_528.

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Holze, Rudolf. "Ionic conductance of cyclohexane-1,1-dicarboxylic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_550.

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Conference papers on the topic "Dicarboxylic"

1

Bian, Wenxin, Junjie Si, and Zugang Liu. "Improved performance of inverted green perovskite light-emitting diodes with dicarboxylic acid additive." In Fourth International Conference on Computer Technology, Information Engineering, and Electron Materials (CTIEEM 2024), edited by Massimo Ficco and Yixian Yang. SPIE, 2025. https://doi.org/10.1117/12.3058493.

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2

Godínez-Alvarez, J. M., J. L. Mora-Mendoza, E. Rodríguez-Betancourt, G. Zavala-Olivares, and Gonzalez-Núñez. "Inhibition of Ferrous Metal Corrosion by Carboxylates." In CORROSION 2004. NACE International, 2004. https://doi.org/10.5006/c2004-04412.

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Abstract A review on inhibitor performance in neutral aqueous solutions of sodium salts of mono and dicarboxylic acids as corrosion inhibitors for mild steel, under static conditions and room temperature, is presented. Electrochemical techniques are nowadays used to study the deaeration effect on passivity for several inhibitors. Recent results showed that oxygen is essential to develop the inhibitive characteristics of several compounds. For example, sebacate and octanoate require significant oxygen levels, whereas 2-ethyl hexanoate and decanoate maintain passivity even at very low oxygen lev

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3

Kostić, Marina D., Jovana S. Marjanović, Sven Mangelinckx, and Vera M. Divac. "In silico Drug-Likeness, Pharmacokinetic and other ADME properties of 2- (aminomethyl)cyclopropane-1,1-dicarboxylic acid." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.455k.

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Herein we present the results of in silico determination of Drug-Likeness, Pharmacokinetic and other ADME properties of 2-(aminomethyl)cyclopropane-1,1-dicarboxylic acid as an example constrained γ-amino dicarboxylic acid. The results of in silico screening of drug-likeness, pharmacokinetic and other ADME (absorption, distribution, metabolism and elimination) properties of 2-(aminomethyl)cyclopropane-1,1-dicarboxylic acid have revealed that this compound is not able to cross the blood-brain barrier, but it shows good solubility and gastrointestinal absorption. The possible target screening has

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4

Kenar, James, David Compton, Steve Peterson, and Frederick Felker. "Inclusion Complexes Between Amylose and Long-chain Dicarboxylic Acids Prepared by Jet Cooking: Characterization and Thermal Properties." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/buzm8236.

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Amylose-fatty acid complexes are well known and are an inherent component within foods that modify starch properties and can influence overall food quality. In contrast, only limited reports examine the complexation of dicarboxylic acids by amylose. This study examines the formation, structure, and thermal stability of amylose-dicarboxylic acid inclusion complexes prepared in aqueous media by steam jet cooking starch with C10, C12, C14, and C16 dicarboxylic acids. These long-chain diacid inclusion complexes can be simply prepared on large scale, isolated in good yields, and their formation was

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Kostić, Marina, Vera Divac, and Sven Mangelinckx. "SYNTHESIS AND CHARACTERIZATION OF PALLADIUM (II)–2- (AZIDOMETHYL)CYCLOPROPANE-1,1-DICARBOXYLIC ACID COMPLEX." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.297k.

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The discovery that palladium complexes possess a wide range of biological activities (from antitumor, -viral, -malarial, -fungal to antimicrobial activities) encourages further research in this scientific field. Herein we describe the synthesis and characterization of a novel palladium (II) complex, using [Pd(dien)Cl]Cl and 2-(azidomethyl)cyclopropane-1,1-dicarboxylic acid (azmcpda) as a ligand. [Pd(dien)Cl]Cl was selected as a starting material taking into consideration its importance as a model for the investigation of the substitution reactions in coordination chemistry and a deeper underst

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Kostić, Marina, Vera M. Divac, Sven Mangelinckx, and Jovana S. Marjanović. "BSA binding of 2-(aminomethyl)cyclopropane-1,1-dicarboxylic acid." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.459k.

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Herein, we present the results of the study devoted to the exploration of BSA binding of 2-(aminomethyl)cyclopropane-1,1-dicarboxylic acid, as an example of constrained γ-amino dicarboxylic acid, and, taking into consideration that the effectiveness of a potential drug depends on its ability to bind to a protein carrier and in that way enable transfer through the blood stream. For the investigation of binding properties, we used the fluorescence emission titration of BSA with a synthesized compound. Considering that the BSA solution shows an intensive fluorescence emission around 360 nm, a dec

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Kaidash, Оksana, Denys Savchenko, Svitlana Kukharenko, Sergiy Skorokhod, and Roman Kurganov. "The effect of refractory fillers on improving the tribotechnical characteristics of antifriction self-lubricating polymer composite coatings." In IXth INTERNATIONAL SAMSONOV CONFERENCE “MATERIALS SCIENCE OF REFRACTORY COMPOUNDS”. Frantsevich Ukrainian Materials Research Society, 2024. http://dx.doi.org/10.62564/m4-ok1748.

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To increase reliability and increase maintenance intervals, it is advisable to switch to dry friction units. The most promising is the development and application of self-lubricating polymer composite coatings. This is especially important for the operation of materials in conditions of high sliding speeds and high temperatures (up to 250 °C). The residual strength of the adhesive bond of the synthesized composites with the materials of the friction pair parts after heat treatment (300 °C, 100 h) was evaluated for 3 composite compositions based on polyimide binding synthesized polyimides with

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Karpenko, Oleksandr, and Sergiy Kovalenko. "Heterocyclization Reactions of 4-Hydrazinoquinazoline with Dicarboxylic Acid Anhydrides." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01395.

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Wang, Lu, Xiuwen Wu, Huanhuan Wang, Bingxu Hou, Can Cai, and Jinlin Zhang. "Reversible Thermochromic and Phase Change Composites Based on Dicarboxylic Acid." In The Second International Conference on Materials Chemistry and Environmental Protection. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0008186501150122.

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Benyei, Gyula, Istvan Jalsovszki, and Katalin Fodor-Csorba. "Structure property relationship study on new cubane-1,4-dicarboxylic acid derivatives." In SPIE Proceedings, edited by Jozef Zmija. SPIE, 2004. http://dx.doi.org/10.1117/12.581058.

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Reports on the topic "Dicarboxylic"

1

Mobley, David P. Biosynthesis of long-chain dicarboxylic acid monomers from renewable resources. Final technical report. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/763082.

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