Relevant bibliographies by topics / Imidazole

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Imidazole'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Imidazole"

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Aly, Ashraf A. "Base Catalyzed Synthesis of Novel Fused-Imidazoles from N-Vinyl-1H-imidazole." Zeitschrift für Naturforschung B 60, no. 1 (2005): 106–12. http://dx.doi.org/10.1515/znb-2005-0116.

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Syntheses of various classes of fused-imidazoles are reported. The key to their successful synthesis depends on the reaction of N-vinyl-1H-imidazole with the π-deficient compounds under basic conditions. Reaction of the target imidazole with 1,1,2,2-tetracyanoethylene and dimethyl acetylenedicarboxylate afforded pyrrolo[1,2-a]imidazoles. On the other site, reaction of the target imidazole with 2-dicyanomethyleneindane-1,3-dione, 2,3-dicyano-1,4-naphthoquinone gave indanylimidazolo- [1,2-a]azepine and imidazolo[2,1-a]phenanthridine derivatives, respectively. Under basic reaction condition, vari
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Ganguly, Swastika, Vatsal Vithlani, Anup Kesharwani, et al. "Synthesis, antibacterial and potential anti-HIV activity of some novel imidazole analogs." Acta Pharmaceutica 61, no. 2 (2011): 187–201. http://dx.doi.org/10.2478/v10007-011-0018-2.

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Synthesis, antibacterial and potential anti-HIV activity of some novel imidazole analogs A series of 1-(2-methyl-4-nitro-imidazol-1-yl)-3-arylaminopropan-2-ones (2a-e), 2-methyl-5-nitro-1-{2-[arylmethoxy] ethyl}-1H-imidazoles (5a-d), and N-(3-hydroxyphenyl)-2-(substituted imidazol-1-yl)alkanamides (8a-e) were synthesized with the aim to develop novel imidazole analogs with broad-spectrum chemotherapeutic properties. Title compounds were evaluated for their anti-HIV and antibacterial activities.
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Lipson, Victoria V., Tetiana L. Pavlovska, Nataliya V. Svetlichnaya, et al. "Novel (2-amino-4-arylimidazolyl)propanoic acids and pyrrolo[1,2-c]imidazoles via the domino reactions of 2-amino-4-arylimidazoles with carbonyl and methylene active compounds." Beilstein Journal of Organic Chemistry 15 (May 6, 2019): 1032–45. http://dx.doi.org/10.3762/bjoc.15.101.

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The unexpectedly uncatalyzed reaction between 2-amino-4-arylimidazoles, aromatic aldehydes and Meldrum’s acid has selectively led to the corresponding Knoevenagel–Michael adducts containing a free amino group in the imidazole fragment. The adducts derived from Meldrum’s acid have been smoothly converted into 1,7-diaryl-3-amino-6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-5-ones and 3-(2-amino-4-aryl-1H-imidazol-5-yl)-3-arylpropanoic acids. The interaction of 2-amino-4-arylimidazoles with aromatic aldehydes or isatins and acyclic methylene active compounds has led to the formation of pyrrolo[1,2-c]imi
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Gerasimova, Elena L., Elena R. Gazizullina, Maria V. Borisova, et al. "Design and Antioxidant Properties of Bifunctional 2H-Imidazole-Derived Phenolic Compounds—A New Family of Effective Inhibitors for Oxidative Stress-Associated Destructive Processes." Molecules 26, no. 21 (2021): 6534. http://dx.doi.org/10.3390/molecules26216534.

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The synthesis of inhibitors for oxidative stress-associated destructive processes based on 2H-imidazole-derived phenolic compounds affording the bifunctional 2H-imidazole-derived phenolic compounds in good-to-excellent yields was reported. In particular, a series of bifunctional organic molecules of the 5-aryl-2H-imidazole family of various architectures bearing both electron-donating and electron-withdrawing substituents in the aryl fragment along with the different arrangements of the hydroxy groups in the polyphenol moiety, namely derivatives of phloroglucinol, pyrogallol, hydroxyquinol, in
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Demchenko, Sergii, Roman Lesyk, Oleh Yadlovskyi, et al. "Synthesis, Antibacterial and Antifungal Activity of New 3-Aryl-5H-pyrrolo[1,2-a]imidazole and 5H-Imidazo[1,2-a]azepine Quaternary Salts." Molecules 26, no. 14 (2021): 4253. http://dx.doi.org/10.3390/molecules26144253.

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A series of novel 3-aryl-5H-pyrrolo[1,2-a]imidazole and 5H-imidazo[1,2-a]azepine quaternary salts were synthesized in 58–85% yields via the reaction of 3-aryl-6, 7-dihydro-5H-pyrrolo[1,2-a]imidazoles or 3-aryl-6,7,8,9-tetrahydro-5H-imidazo[1,2-a]azepines and various alkylating reagents. All compounds were characterized by 1H NMR, 13C NMR, and LC-MS. The conducted screening studies of the in vitro antimicrobial activity of the new quaternary salts derivatives established that 15 of the 18 newly synthesized compounds show antibacterial and antifungal activity. Synthesized 3-(3,4-dichlorohenyl)-1
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Aonofriesei, Florin. "Increased Absorption and Inhibitory Activity against Candida spp. of Imidazole Derivatives in Synergistic Association with a Surface Active Agent." Microorganisms 12, no. 1 (2023): 51. http://dx.doi.org/10.3390/microorganisms12010051.

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This paper’s purpose was to evaluate the interaction between three imidazole derivatives, (2-methyl-1H-imidazol-1-yl)methanol (SAM3), 1,1′-methanediylbis(1H-benzimidazole (AM5) and (1H-benzo[d]imidazol-1-yl)methanol 1-hydroxymethylbenzimidazole (SAM5) on the one hand, and sodium dodecyl sulphate (SDS) on the other, as antifungal combinations against Candida spp. Inhibitory activity was assessed using the agar diffusion method and Minimal Inhibitory Concentration (MIC) and showed moderate inhibitory activity of single imidazole derivatives against Candida spp. The mean value of MIC ranged from
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Zhou, Qifan, Fangyu Du, Yajie Shi, Ting Fang, and Guoliang Chen. "Synthesis and Analysis of 1-Methyl-4-Phenyl-1H-Imidazol-2-Amine." Journal of Chemical Research 42, no. 12 (2018): 608–10. http://dx.doi.org/10.3184/174751918x15414286606248.

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A practical synthetic route to an important pharmaceutical intermediate 1-methyl-4-phenyl-1H-imidazol-2-amine, via a three-step sequence involving cyclisation, hydrolysis and methylation, is reported. In the process of optimisation, a novel chemical entity was isolated and confirmed to be 2,6-diphenyl-1H-imidazo[1,2-a]imidazole by MS, 1H NMR and 13C NMR. The scale-up experiment was carried out to provide 1-methyl-4-phenyl-1H-imidazol-2-amine in 27.4% total yield.
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Loubidi, M., M. Lorion, A. El Hakmaoui, P. Bernard, M. Akssira, and G. Guillaumet. "One-Step Synthesis of 1H-Imidazo[1,5-a]imidazole Scaffolds and Access to their Polyheterocycles." Synthesis 51, no. 21 (2019): 3973–80. http://dx.doi.org/10.1055/s-0039-1690182.

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In this work, we continue our adventure in the chemistry of 5-5 tri-nitrogen bicycles. We disclose herein a one-step reaction to synthesize 1H-imidazo[1,5-a]imidazoles with different substituents introduced through the use of a wide range of aldehydes and isocyanides by using a Groebke–Blackburn–Bienaymé multicomponent reaction. The aim is to build a new library of 1H-imidazo[1,5-a]imidazole scaffolds. This bicycle was then modified to access new nitrogen-containing polycyclic compounds.
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Arduengo, Anthony J., Jens R. Goerlicha, Fredric Davidson, and William J. Marshall. "Carbene Adducts of Dimethylcadmium." Zeitschrift für Naturforschung B 54, no. 11 (1999): 1350–56. http://dx.doi.org/10.1515/znb-1999-1102.

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The first examples of carbene-cadmium complexes are reported from the reactions of a variety of imidazol-2-ylidenes or imidazolin-2-ylidenes with dimethylcadmium. Four new carbene complexes are characterized by NMR spectroscopy (1H , 13C and 113Cd). The cadmium centers are strongly shifted downfield (100 -150 ppm) by interaction with the carbenes. X-ray structures are reported for three carbene-cadmium 1:1 adducts. The cadmium centers exhibit distorted trigonal-planar geometries in which the carbene ligands have an average 18.2 pm longer bond distance to cadmium compared to the methyl groups.
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Mlostoń, Grzegorz, Małgorzata Celeda, Katarzyna Urbaniak, et al. "Synthesis and selected transformations of 2-unsubstituted 1-(adamantyloxy)imidazole 3-oxides: straightforward access to non-symmetric 1,3-dialkoxyimidazolium salts." Beilstein Journal of Organic Chemistry 15 (February 19, 2019): 497–505. http://dx.doi.org/10.3762/bjoc.15.43.

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Adamantyloxyamine reacts with formaldehyde to give N-(adamantyloxy)formaldimine as a room-temperature-stable compound that exists in solution in monomeric form. This product was used for reactions with α-hydroxyiminoketones leading to a new class of 2-unsubstituted imidazole 3-oxides bearing the adamantyloxy substituent at N(1). Their reactions with 2,2,4,4-tetramethylcyclobutane-1,3-dithione or with acetic acid anhydride occurred analogously to those of 1-alkylimidazole 3-oxides to give imidazol-2-thiones and imidazol-2-ones, respectively. Treatment of 1-(adamantyloxy)imidazole 3-oxides with
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Dissertations / Theses on the topic "Imidazole"

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Siamaki, Ali Reza 1965. "The palladium catalyzed multicomponent synthesis of imidazoles and imidazole-containing [pi]-conjugated polymers /." Thesis, McGill University, 2008. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=115851.

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The primary goal of this study is to develop novel metal catalyzed multicomponent reaction methods to generate imidazoles and their derivatives. This is directed towards the assembly of poly-substituted imidazoles, imidazolones and imidazole-containing pi-conjugated polymers. These products are generated in one-pot from such basic components as imines, acid chlorides, carbon monoxide, and/or organostannanes, via the use of palladium catalysis.<br>In Chapter 2, the design of a new palladium catalyzed synthesis of highly substituted imidazoles from imines and acid chlorides is described. This re
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Smith, Matthew R. "Studies in imidazole chemistry." Thesis, University of Nottingham, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555805.

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A brief introduction to imidazole is given, outlining its physical and chemical properties since its discovery in 1858. The role of imidazole in the natural amino acid (S)-histidine is discussed with reference to its use in catalytic triads and histidine proton shuttles. The decarboxylation of (S)-histidine to give histamine and its importance in biological functions is also discussed with reference to the development of the histamine H2- receptor antagonist Cimetidine and other imidazole containing drugs. In Chapter 1 the chemistry of 5-diazoimidazoles and the resulting imidazolylidene carben
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Thomason, Matthew James. "Soft X-ray spectroscopy of molecular species in solution : studies of imidazole and imidazole/water systems." Thesis, University of Manchester, 2013. https://www.research.manchester.ac.uk/portal/en/theses/soft-xray-spectroscopy-of-molecular-species-in-solution-studies-of-imidazole-and-imidazolewater-systems(ae99d759-ca04-4e9a-b585-7a91b8aa2929).html.

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Soft X-ray near-edge X-ray absorption fine-structure (NEXAFS) spectroscopy of liquids, an emerging synchrotron radiation technique, has been applied to characterise the local environment of imidazole in aqueous solution to elucidate the structural nature of the well known self-association effects in this system. Atomic core level spectroscopies such as NEXAFS are extremely sensitive to short range structure, including bond lengths and angles as well as coordination numbers, in condensed matter and in molecular systems.N K-edge NEXAFS data were successfully acquired for aqueous imidazole soluti
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Mongeot, Alexandre. "Synthèse, réactivité et intérêts pharmacologiques de nouvelles imidazo[-x]azines et de nouveaux imidazoles." Strasbourg 1, 2006. http://www.theses.fr/2006STR13254.

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Moody, David John. "Studies of some fused imidazole derivatives." Thesis, University of St Andrews, 1986. http://hdl.handle.net/10023/11011.

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The main synthetic routes to benzimidazole N-oxides are outlined and some indication is given as to the current and potential pharmacological usefulness of such materials. A claim that 4-methyl-2-nitrophenylglycine is cyclised in acetic anhydride to give either 5-methylbenzimidazole 3-oxide or the isomeric 5 methylbenzimidazolone was investigated. This work was found to be impossible to duplicate. It is established that, by employing flash vacuum pyrolysis, the claimed products can be obtained thermolytically from the starting glycine. This is the first recorded example of the formation of an
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Gonçalves, Marcos Brown. "Efeitos de estado sólido e ligações de hidrogênio sobre o gradiente de campo elétrico no núcleo no imidazol." Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/43/43134/tde-09022007-124016/.

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Estudamos as propriedades eletrônicas, estruturais e hiperfinas, nos sítios de nitrogênio, para o composto imidazol nas fases gasosa e sólida. Utilizamos o método PAW que é um método ab initio all-electron, dentro da Teoria do Funcional da Densidade, através do código computacional CP-PAW. Nossos valores, tanto para a fase gasosa quanto para a fase cristalina do gradiente de campo elétrico no núcleo, de freqüência de acoplamento quadrupolar (&#957;) e parâmetro de assimetria (&#951;) estão em ótima concordância com os resultados experimentais da literatura e são os primeiros resultados obtidos
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Mercier, Nathalie. "Les dérivés de l'imidazole dans le traitement des mycoses : chimie, dosages, applications thérapeutiques." Bordeaux 2, 1997. http://www.theses.fr/1997BOR2P025.

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Wells, Doran K. "Synthesis of imidazole derivatives related to pinacidil." Thesis, Heriot-Watt University, 1993. http://hdl.handle.net/10399/1413.

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Biard, Olivier. "Hépatotoxicité des imidazoles." Paris 5, 1995. http://www.theses.fr/1995PA05P146.

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Roberts-McDaniel, Patricia D. "Physical and mechanical behavior of amorphous poly(arylene ether-co-imidazole)s and poly(arylene ether-co-imidazole) modified epoxies." W&M ScholarWorks, 1994. https://scholarworks.wm.edu/etd/1539623850.

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Due to the high crosslink density of cured epoxy resins they generally lack damage tolerance. A significant amount of research has been expended to improve the toughness of epoxies. Research into the area of thermoplastic epoxy modifiers has begun to overcome some of the limitations of early methods of epoxy toughening (i.e. lower modulus and thermal stability).;This study examines the physical and mechanical properties of random poly(arylene ether-co-imidazole) (PAE-co-Is) and the characterization of epoxies modified with poly(arylene ether-co-imidazole)s.;Poly(arylene ether-co-imidazole)s ex
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Books on the topic "Imidazole"

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Preston, P. N. Condensed imidazoles: 5-5 ring systems. Wiley, 1986.

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Grimmett, M. R. Imidazole and benzimidazole synthesis. Academic Press, 1997.

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Preedy, Victor R., ed. Imidazole Dipeptides. Royal Society of Chemistry, 2015. http://dx.doi.org/10.1039/9781782622611.

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L, Shaner Dale, and O'Connor Susan L, eds. The Imidazolinone herbicides. CRC Press, 1991.

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McMaster, Jonathan. Copper and Zinc complexes of bi-imidazole ligands. University of Manchester, 1995.

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International Symposium on Agmatine and Imidazoline Systems (4th 2003 San Diego, Calif.). Agmatine and imidazolines: Their novel receptors and enzymes. New York Academy of Sciences, 2003.

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G, Bartholini, ed. Imidazopyridines in anxiety disorders: A novel experimental and therapeutic approach. Raven Press, 1993.

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Bhalla, Rajiv. Copper and zinc complexes of Bis- and Tris-imidazole ligands. University ofManchester, 1995.

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Kawamoto, Yusuke. Synthesis and Biological Evaluation of Pyrrole–Imidazole Polyamide Probes for Visualization of Telomeres. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-6912-4.

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1931-, Volodarsky Leonid B., ed. Imidazoline nitroxides. CRC Press, 1988.

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Book chapters on the topic "Imidazole"

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Gooch, Jan W. "Imidazole." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_13980.

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Bährle-Rapp, Marina. "Imidazole." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_5154.

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Berdimuradov, Khasan, Elyor Berdimurodov, Ilyos Eliboev, et al. "Imidazole- and Imidazoline-based Corrosion Inhibitors." In Handbook of Heterocyclic Corrosion Inhibitors. CRC Press, 2023. http://dx.doi.org/10.1201/9781003377016-4.

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Champagne, Trevor. "Antifungal, Imidazole." In Litt's Drug Eruption & Reaction Manual, 31st ed. CRC Press, 2025. https://doi.org/10.1201/9781003569756-1506.

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Kumar, Vipan, and Mohinder P. Mahajan. "Pyrimidine and Imidazole." In Heterocycles in Natural Product Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634880.ch14.

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Schomburg, Dietmar, and Dörte Stephan. "Imidazole N-acetyltransferase." In Enzyme Handbook 11. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61030-1_134.

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Dilworth, J. R., and S. Morton. "From Imidazole Complexes." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145227.ch19.

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Schomburg, Dietmar, and Dörte Stephan. "Purine imidazole-ring cyclase." In Enzyme Handbook 17. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-58969-0_38.

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Vlassov, V. V., and A. V. Vlassov. "Cleavage of RNA by Imidazole." In Artificial Nucleases. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18510-6_5.

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Abe, Jiro. "Fast Photochromism of Bridged Imidazole Dimers." In New Frontiers in Photochromism. Springer Japan, 2013. http://dx.doi.org/10.1007/978-4-431-54291-9_9.

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Conference papers on the topic "Imidazole"

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Silva, Elaine F., Julio S. Wysard, Tatiana C. Almeida, Merlin C. E. Bandeira, and Oscar R. Mattos. "On the Inhibition Efficiency of Different Imidazole-Based Green Corrosion Inhibitors: Insights from Raman Spectroscopy and Electrochemical Techniques." In LatinCORR 2023. AMPP, 2023. https://doi.org/10.5006/lac23-20533.

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Extended Abstract Adsorption of imidazole, 4-methylimidazole and guanine on copper in chloride solutions was investigated by a combination of weight loss tests with electrochemical and Raman techniques to understand their inhibition efficiency and interaction with the metal. Results revealed that imidazole and 4-methyimidazole are inefficient while guanine was an efficient inhibitor (86 %) due to formation of a passive film. Guanine was not efficient towards API 5L X65 steel corrosion in HCl (~22 %) and the low efficiency was due to physisorption. The insights obtained with the combination of
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Mannan, Abdul, A. C. Ferrel-Alvarez, Victor H. Ponce Valderrama, and H. Castaneda. "Interfacial Characterization of C1018 Using Ionic Liquids and Organic Imidazoline Compound." In CONFERENCE 2025. AMPP, 2025. https://doi.org/10.5006/c2025-00608.

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Abstract In the recent development of advanced chemicals used to influence the electrolyte/substrate interface; novel ILs have made subsequent progress in affecting the kinetics of the electrochemical reactions in a sustainable manner. In this research, the Imidazole-based IL [EMIM Ac] and conventional organic Imidazoline inhibitor were investigated for their effectiveness upon carbon steel alloy C1018 coupons in a 3.5 wt% NaCl environment. To study their corrosion behavior, electrochemical techniques were employed at a stationary state, maintaining 60°C with increasing inhibitor concentration
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Velasco-Bolom, Pedro Marcos, Jorge Luis Camas-Anzueto, Madaín Pérez-Patricio, Joel Gómez-Pérez, and Marcoantonio Ramírez-Morales. "Thermo-optical characterization of a new imidazole derivative for application in fiber optic sensors." In Latin America Optics and Photonics Conference. Optica Publishing Group, 2024. https://doi.org/10.1364/laop.2024.tu4a.17.

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In this work, a new imidazole derivative is characterized in a 30° to 65 °C temperature range. It shows thermochromic properties in its absorption spectrum to be used in manufacturing fiber optic sensors.
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Olivo, J. M. Domínguez, Shuyun Cao, D. Young, B. Brown, and S. Nesic. "Effect of Corrosion Inhibitor Head Group on the Electrochemical Processes Governing CO2 Corrosion." In CORROSION 2020. NACE International, 2020. https://doi.org/10.5006/c2020-14925.

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Abstract The use of corrosion inhibitors is a common practice used to mitigate internal pipeline corrosion in the oil and gas industry. An organic corrosion inhibitor is a molecule comprised of a head group (hydrophilic part) and an alkyl tail (hydrophobic part). Despite the significant amount of work associating the effect of the head group with the mode of adsorption of the inhibitor (such as bonding, effect on the tilt angle of the tail, and hysteresis), there is a lack of research relating the effect of the head group with the electrochemical processes governing the corrosion of mild steel
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Robbiani, Baptiste, Jean-Louis Augé, and Gilbert Teyssèdre. "Mechanoluminescence of Anhydride and Imidazole Cured Epoxies Under the Combined Effect of Thermal and Cyclic Mechanical Stresses." In 2024 IEEE 5th International Conference on Dielectrics (ICD). IEEE, 2024. http://dx.doi.org/10.1109/icd59037.2024.10613105.

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Tsuri, S., K. Takao, and K. Mochizuki. "Effect of Primer Composition on Cathodic Disbonding Resistance and Adhesion Durability of Three Layer Polyethylene Coated Steel Pipe." In CORROSION 1998. NACE International, 1998. https://doi.org/10.5006/c1998-98497.

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Abstract The cathodic disbonding resistance and adhesion durability of three layer polyethylene coated steel pipe were studied from the viewpoint of water permeability and the water uptake of dicyandiamide-imidazole cured epoxy primer. The reaction between the epoxy resin and dicyandiamide generates hydroxyl groups. Therefore, as the content of dicyandiamide increased, the water uptake of the primer increased and the water diffusion rate of the primer decreased because of the strong interaction between hydroxyl reaction product and water molecules. Excellent cathodic disbonding resistance and
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Yang, Dongrui, Omar Rosas, and Homero Castaneda. "Comparison of the Corrosion Inhibiting Properties of Imidazole Based Ionic Liquids on API X52 Steel in Carbon Dioxide Saturated NaCl Solution." In CORROSION 2014. NACE International, 2014. https://doi.org/10.5006/c2014-4357.

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Abstract The aim of this work is to investigate the corrosion inhibiting efficiency of four imidazolium ionic liquids in carbon dioxide saturated NaCl Brine solution by using electrochemical and surface analysis testing methods. The four compounds are 1-Ethyl-3-methylimidazolium chloride (Emc), 1-Butyl-3-methylimidazolium chloride (Bmc), 1-Hexyl-3-methylimidazolium chloride (Hmc), and 1-Decyl-3-methylimidazolium chloride (Dmc). Under the testing conditions, compound Dmc showed the highest inhibition efficiency. After 24 hours of immersion time in the inhibiting solution, the inhibiting efficie
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Codescu, Marius-Andrei, Moritz Weiß, Martin Brehm, Oleg Kornilov, Daniel Sebastiani, and Erik T. J. Nibbering. "Ultrafast Proton Transfer Pathways Mediated by Imidazole." In International Conference on Ultrafast Phenomena. Optica Publishing Group, 2022. http://dx.doi.org/10.1364/up.2022.tu1a.4.

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We explore with ultrafast infrared spectroscopy and molecular dynamics simulations how imidazole, an amphoteric molecule that can act both as acid and as base, provides alternate proton transfer pathways in the tautomerization reaction of 7-hydroxyquinoline.
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Bel'skaya, L. "PREDICTIVE SIGNIFICANCE OF BIOCHEMICAL MARKERS OF SALIVA IN PATIENTS WITH LUNG CANCER COMBINED WITH COPD." In XIV International Scientific Conference "System Analysis in Medicine". Far Eastern Scientific Center of Physiology and Pathology of Respiration, 2020. http://dx.doi.org/10.12737/conferencearticle_5fe01d9c2a59e1.13232371.

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A complex of salivary biochemical parameters, which have prognostic value in lung cancer, was revealed. Therefore, for the group of patients without COPD, these indicators include imidazole compounds and LDH, with mild COPD - only imidazole compounds, with moderate COPD - pH and LDH. This is the first time that such prognostic results were obtained using saliva.
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Aulakh, Ramanpreet Kaur, Aman Mahajan, Subodh Kumar, and Gurpreet Singh. "Charge transport properties of single layer imidazole-based devices." In ADVANCED MATERIALS AND RADIATION PHYSICS (AMRP-2020): 5th National e-Conference on Advanced Materials and Radiation Physics. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0053268.

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Reports on the topic "Imidazole"

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Adigun, Risikat. Insight into the Reactivity of Metastasis Inhibitor, Imidazolium trans-[tetrachloro (dimethyl sulfoxide)(imidazole)ruthenate(III)], with Biologically-active Thiols. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.378.

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Ramakrishnan, V. T., M. Vedachalam, and J. H. Boyer. Dense Compounds of C, H, N, and O Atoms. 2. Nitramine and Nitrosamine Derivatives of 2-Oxo- and 2-Iminooctahydroimidazo(4,5-d)Imidazole. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada238856.

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Sherrill, William M., and Eric C. Johnson. A New Method for the Production of Tetranitroglycoluril From Imidazo-[4,5-d]-Imidazoles With the Loss of Dinitrogen Oxide. Defense Technical Information Center, 2014. http://dx.doi.org/10.21236/ada598881.

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Musselman, Inga H. Novel Zeolitic Imidazolate Framework/Polymer Membranes for Hydrogen Separations in Coal Processing. Office of Scientific and Technical Information (OSTI), 2013. http://dx.doi.org/10.2172/1091874.

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Yaghi, Omar M. Metal-organic and zeolite imidazolate frameworks (MOFs and ZIFs) for highly selective separations. Office of Scientific and Technical Information (OSTI), 2012. http://dx.doi.org/10.2172/1050881.

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McGuirk, Christopher. Final Technical Report: High Capacity Step-Shaped Hydrogen Adsorption in Robust, Pore-Gating Zeolitic Imidazolate Frameworks. Office of Scientific and Technical Information (OSTI), 2025. https://doi.org/10.2172/2520056.

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