Academic literature on the topic 'Thiazole Derivatives'

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Journal articles on the topic "Thiazole Derivatives"

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Borde, Ramesh M., Satish B Jadhav, Rahul R Dhavse, and Achut S Munde. "DESIGN, SYNTHESIS, AND PHARMACOLOGICAL EVALUATION OF SOME NOVEL BIS-THIAZOLE DERIVATIVES." Asian Journal of Pharmaceutical and Clinical Research 11, no. 4 (2018): 164. http://dx.doi.org/10.22159/ajpcr.2018.v11i4.23413.

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Objective: A series of substituted 5,2-bis-thiazoles derivatives were synthesized by Hantzsch reaction and evaluated in vitro for antimicrobial activity against Escherichia coli, Pseudomonas aeruginosa, Bacillus subtilis, and Staphylococcus aureus. Methods: 2-(4-(benzyloxy)phenyl)-4-methylthiazole-5-carbothioamide were synthesized and allowed to react with various α-haloketones to give 5,2-bis-thiazoles, i.e., 2-(4-(benzyloxy)phenyl)-4-methyl-5-(4-substituted thiazol-2-yl)thiazole derivatives in excellent yield. The synthesized compounds were characterized by spectroscopic methods as well as e
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Mohareb, Rafat M., Amira E. M. Abdallah, and Ebtsam A. Ahmed. "Synthesis and cytotoxicity evaluation of thiazole derivatives obtained from 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene- 3-carbonitrile." Acta Pharmaceutica 67, no. 4 (2017): 495–510. http://dx.doi.org/10.1515/acph-2017-0040.

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Abstract Reactivity of 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3- carbonitrile towards thioglycolic acid resulted in thiazole derivative 1. The latter reacted with different chemical reagents to give thiazole, pyrano[2,3-d]thiazole and thiazolo[ 4,5-d]thiazole derivatives. Cytotoxicity effects of the newly synthesized products against six cancer cell lines, namely, human gastric cancer (NUGC), human colon cancer (DLD- 1), human liver cancer (HA22T and HEPG-2), human breast cancer (MCF) and nasopharyngeal carcinoma (HONE-1) as well as against a normal fibroblast cell (WI-38) were evaluated.
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Erguc, Ali, Mehlika Dilek Altintop, Ozlem Atli, et al. "Synthesis and Biological Evaluation of New Quinoline-Based Thiazolyl Hydrazone Derivatives as Potent Antifungal and Anticancer Agents." Letters in Drug Design & Discovery 15, no. 2 (2018): 193–202. http://dx.doi.org/10.2174/1570180814666171003145227.

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Background: In medicinal chemistry, thiazoles have gained great importance in antifungal and anticancer drug design and development. Objectives: The aim of this study was to synthesize new quinoline-based thiazolyl hydrazone derivatives and evaluate their anticandidal and anticancer effects. Methods: New thiazolyl hydrazone derivatives were evaluated for their anticandidal effects using disc diffusion method. Ames MPF assay was carried out to determine the genotoxicity of the most effective antifungal derivative. MTT assay was also performed to assess the cytotoxic effects of the compounds on
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Ram, Sevak Verma*1 Nitin Mittal2 Bhumika Yogi3 Shikha Sharma4 Abhishek Mishra5. "A Review On Chemistry And Antimicrobial Activity Of Thiazole." International Journal in Pharmaceutical Sciences 2, no. 3 (2024): 1184–201. https://doi.org/10.5281/zenodo.10893122.

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The recent study classe of five-membered heterocyclic compounds is thiazoles. Several thiazoles, both synthetic and natural, and their derivatives exhibited strong biological activity. Thiazole derivatives exhibit strong antibacterial action against a variety of bacterial species & diseases because of their special characteristics. As a result, the current study assigns different thiazoles and there derivatives' antimicrobial activity. Through the use of many databases, every pertinent piece of literature has been examined. The important studies on the antibacterial activity of thiazole de
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Tokárová, Zita, and Anna Biathová. "Synthesis and structure-physicochemical properties relationship of thiophene-substituted bis(5,4-d)thiazoles." Nova Biotechnologica et Chimica 17, no. 2 (2018): 193–200. http://dx.doi.org/10.2478/nbec-2018-0020.

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Abstract Substituted thiophene-2-carbaldehydes 1a-dwere utilized in the synthesis of symmetrically substituted thiazolo[5,4-d]thiazoles 3a-d. Bis(5,4-d)thiazoles with thiophene core at the termini are the most employed in the chemistry of materials but exhibit insufficient solubility in majority of organic solvents with notable impact on the low yields of products. Accordingly, the synthetic approach towards 2,5-dithiophen- 2-yl-thiazolo[5,4-d]thiazole (3a) and its substituted derivatives 3b-d is discussed under the various reaction conditions. Appropriate structural characterisations are incl
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Nayak, Swarnagowri, and Santhosh L. Gaonkar. "A Review on Recent Synthetic Strategies and Pharmacological Importance of 1,3-Thiazole Derivatives." Mini-Reviews in Medicinal Chemistry 19, no. 3 (2019): 215–38. http://dx.doi.org/10.2174/1389557518666180816112151.

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Thiazole is the most common heterocyclic compound in heterocyclic chemistry and in drug design. Presence of several reaction sites in the thiazole moiety extends their range of applications and leads to new solutions for challenges in synthetic and medicinal chemistry. Thiazole derivatives are widely used as bioactive agents, liquid crystals, sensors, catalysts, etc. The motivating molecular architecture of 1,3-thiazoles makes them suitable moieties for drug development. In this review, our aim is to corroborate the recent data available on various synthetic strategies and biological propertie
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Dekate, Shital M., Kishor M. Hatzade, and Ajay M. Ghatole. "A Facile Synthesis of Thiazole Derivatives bearing Imidazole Moiety, Schiff Bases and their O-Glucosides." Asian Journal of Chemistry 35, no. 1 (2022): 29–38. http://dx.doi.org/10.14233/ajchem.2023.24049.

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A unique approach for the synthesis of new thiazole O-glycosides is presented in this work. 2-Amino-4-hydroxy-phenyl-1,3-thiazole-5-carboxaldehyde (3a) was reacted with phenyl glyoxal and benzil to form 4-(4-hydroxy-phenyl)-5-(4-phenyl-1H-imidazol-2-yl)-thiazol-2-amine (4a) and 4-(4-hydroxy-phenyl)-5-(4,5-diphenyl-1H-imidazol-2-yl)-thiazol-2-amine (4b), respectively. A series of substituted Schiff bases of 4a and 4b were synthesized reacting with various aryl aldehyde to form 2-(imino substituted benzal)-4-(4-hydroxy-phenyl)-5-(4-phenyl-1H-imidazol-2-yl)-thiazoles (5a-e) and 2-(imino substitut
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Rayala, Ramanjaneyulu, Prakash Chaudhari, Ashley Bunnell, Bracken Roberts, Debopam Chakrabarti, and Adel Nefzi. "Parallel Synthesis of Piperazine Tethered Thiazole Compounds with Antiplasmodial Activity." International Journal of Molecular Sciences 24, no. 24 (2023): 17414. http://dx.doi.org/10.3390/ijms242417414.

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Thiazole and piperazine are two important heterocyclic rings that play a prominent role in nature and have a broad range of applications in agricultural and medicinal chemistry. Herein, we report the parallel synthesis of a library of diverse piperazine-tethered thiazole compounds. The reaction of piperazine with newly generated 4-chloromethyl-2-amino thiazoles led to the desired piperazine thiazole compounds with high purities and good overall yields. Using a variety of commercially available carboxylic acids, the parallel synthesis of a variety of disubstituted 4-(piperazin-1-ylmethyl)thiazo
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Yadav, Pradeep, and Y. C. Joshi. "Synthesis and Spectral Study of Novel Norfloxacin Derivatives." E-Journal of Chemistry 5, s2 (2008): 1154–58. http://dx.doi.org/10.1155/2008/357073.

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Reaction of [1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-quinolone-3-carboxylic acid (norfloxacin) with thiazole / benzothiazole diazonium chloride to get new piperazine substituted norfloxacin derivative. These norfloxacin derivatives were further condensed with variousβ-diketone to get novel acid derivatives of 1-Ethyl-6-fluoro-4-oxo-7- [4 (thiazol-2-yldiazenyl)-piperzin-1-yl]-1,4-dihydro-quinoline-3-carboxylic acid (6a-e) and 7-(4-(benzo[d]thiazol-2-yldiazenyl)piperazin-1-yl)-1-ethyl-6-fluoro-4-oxo-1, 4-dihydroquinoline-3-carboxylic acid (6 f-j). Structures of these compounds were
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Wadave, Disha. "Molecular docking study of 2,4 disubstituted thiazole derivatives as antiulcer activity." International Journal of Biology and Chemistry 17, no. 2 (2024): 154–57. https://doi.org/10.26577/ijbch2024v17.i2.12.

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In this study, 2,4 disubstituted thiazole derivatives were used to create an antiulcer agent. These compounds were chosen based on molecular properties and a drug-likeness score, ensuring their suitability for oral absorption. The molecular docking of 2,4 disubstituted thiazole derivatives was performed using AutoDock Vina Ver.1.1.2. The thiazole derivatives were constructed using Cambridge's Chem Draw Ultra 8.0 software. The program Chem 3D Ultra 8.0 was used to convert 2D structures to 3D structures. Thiazole derivatives were docked into the H2 blocker, with nizatidine binding at the active
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Dissertations / Theses on the topic "Thiazole Derivatives"

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Ishita, Keisuke. "Design, Synthesis and Evaluation of Carborane and Thiazole Derivatives." The Ohio State University, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=osu1510937794366855.

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Yang, Dazhou. "Synthesis and biophysical evaluation of thiazole orange derivatives as DNA binding ligands." Scholarly Commons, 2014. https://scholarlycommons.pacific.edu/uop_etds/141.

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Guanine-rich telomeric DNA at the end of chromosomes can form a unique DNA tertiary structure - G-quadruplex, which is known to inhibit the binding of telomerase to telomeric regions in cancer cells and thus regulate unrestricted cancer cell growth. Hence, G-quadruplex DNA has recently become a promising target in oncology. The formation of G-quadruplex structures is greatly facilitated by G-quadruplex binding ligands such as Thiazole orange (TO). Compared with other G-quadruplex binding ligands, TO has an intriguing tunable fluorescence property. Upon binding to DNA, the fluorescence of TO ca
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Hakizimana, Emmanuel Victor. "Synthesis, characterisation and evaluation of novel ferrocene-thiazole derivatives as antiplasmodial agents." Thesis, Rhodes University, 2017. http://hdl.handle.net/10962/5304.

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Malaria is mosquito-transmitted disease which continues to pose threat to humanity, despite the efforts undertaken by the scientific community, government entities and international organizations. The major problem is that Plasmodium species have developed resistance against available drugs. In order to counter this problem, antimalarial drugs that are efficacious and with novel mode of action are of great necessity. Thiazole derivatives, in particular aminomethylthiazole analogues, have been shown to exhibit promising antimalarial activity against Plasmodium falciparum strains. Previous studi
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Mjambili, Faith Riziki. "Synthesis and biological evaluation of thiazole and metergoline derivatives as antimycobacterial and antiplasmodial agents." Master's thesis, University of Cape Town, 2013. http://hdl.handle.net/11427/6635.

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TB patients show poor compliance to available drugs due to the costs, adverse side effects, and prolonged treatment, leading to multi-drug resistant (MDR), extensively drug resistant (XDR), and most recently totally drug resistant TB. Shared drug toxicities and drug interactions with antiretrovirals compound the problem. The rapid development of resistance to known antimalarials compared to the rate at which new agents are coming into the market still remains a big challenge is combating malaria. Currently, with resistance to ACTs having been documented in South-East Asia, the situation is dir
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Hanafi-Bagby, Dalia. "Towards a fibre optic nucleic acid biosensor, thiazole orange derivatives as sensitive fluorescent probes to detect DNA hybridization." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape10/PQDD_0016/MQ45848.pdf.

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Olszewski, Tomasz Krzysztof. "Original syntheses of new biomolecules : from imidazole and thiazole derivatives of α-aminophosphonic acids and γ-amino-α, β-dihydroxy carboxylic acid derivatives to disaccharide mimics". Montpellier 2, 2006. http://www.theses.fr/2006MON20017.

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Bzeih, Tourin. "Methodologies involving N-tosylhydrazones for the synthesis of new isocombretastatin A-4 analogs, and the synthesis of thiazole derivatives for antitumor application." Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLS488.

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Ce document de thèse est divisé en deux parties indépendantes, la première partie décrit la synthèse et l'évaluation biologique de nouveaux analogues du composé anti-vasculaire, l'isocombretastatine A-4. Ce travail se situe à l'interface entre la chimie et la biologie.Des réactions séquentielles monotopes mettant en œuvre des réactions de couplage pallado-catalysées entre des N-tosylhydrazones et divers bromure de nitro-aryles et bromure de nitro-biaryles suivies d'une cyclisation réductrice ont conduit à la synthèse d’une chimiothèque d'indoles C2-, C3-, N-aryles et des carbazoles de vinyle a
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Richter, Frank. "Development of the Solution-Spray Flash-Vacuum-Pyrolysis Technique in the Synthesis of Allenyl Isothiocyanates and Synthesis of Complex 2-Amino-1,3-thiazole Derivatives." Doctoral thesis, Universitätsbibliothek Chemnitz, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-175339.

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Gas-phase thermolysis is a long-known and well established method for the preparation of reactive species. It is, however, limited to relatively volatile substances, which are easily vaporised. In the present work, the solution-spray technique for preparative scale was developed. With this technique, it is possible to subject low-volatile substances, which hardly vaporise even under high-vacuum conditions, to gas-phase thermolysis. By utilising oil nozzles used in heating and burner systems, it was possible to integrate a stable solution-spray into the existing flash-vacuum-pyrolysis system. T
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Richter, Frank [Verfasser], Klaus [Akademischer Betreuer] Banert, Klaus [Gutachter] Banert, and Evgeny [Gutachter] Kataev. "Development of the Solution-Spray Flash-Vacuum-Pyrolysis Technique in the Synthesis of Allenyl Isothiocyanates and Synthesis of Complex 2-Amino-1,3-thiazole Derivatives / Frank Richter ; Gutachter: Klaus Banert, Evgeny Kataev ; Betreuer: Klaus Banert." Chemnitz : Universitätsbibliothek Chemnitz, 2015. http://d-nb.info/1213813514/34.

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許峻維. "Synthesis and properties of thiazole Derivatives." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/24292441602040146657.

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碩士<br>國立臺灣科技大學<br>纖維及高分子工程系<br>90<br>In this study, we herein to synthesize the intermediate of 2,4-thiazolidinedion 3 that was given by the thiourea condensed with mono chloroacetic acid in aqueous solution at reflux. Furthermore, the raw materials of acetophenone and 4-chloroaceto-phenone used was used by fused method to synthesize of compound 6a~6b. First,the 2,4-thiazolidinedion 3 and was condensed with the aldehyde in ethanol under the base catalyst to obtain the compound 8a~8f of methine . Besides, the coupling reaction was proceed with the diazonium salt at temperature 0~5℃ t
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Books on the topic "Thiazole Derivatives"

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 3. Wiley & Sons, Incorporated, John, 2008.

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 1. Wiley & Sons, Incorporated, John, 2009.

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 1. Wiley & Sons, Incorporated, John, 2008.

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 2. Wiley & Sons, Incorporated, John, 2009.

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 2. Wiley & Sons, Limited, John, 2007.

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Thiazole and Its Derivatives, Part 3. Wiley & Sons, Incorporated, John, 2009.

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Karam, Nisreen H., Jumbad H. Tomma, and Ammar H. Al-Dujaili. Liquid Crystals of 2,4-Substituted-1,3-Thiazole Derivatives: Synthesis, Characterization and Liquid Crystalline Properties of Some 2,4-Substituted-1,3-Thiazole Derivatives. Scholars' Press, 2014.

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Towards a fibre optic nucleic acid biosensor: Thiazole organge derivatives as sensitive fluorescent probes to detect DNA hybridization. National Library of Canada, 1998.

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Book chapters on the topic "Thiazole Derivatives"

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Xu, Zhengshuang, and Tao Ye. "Thiazoline and Thiazole and their Derivatives." In Heterocycles in Natural Product Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634880.ch13.

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Aune, Jean Pierre, Henri Jean-Marie Dou, and Jacqueline Crousier. "Alkyl, Aryl, Aralkyl, and Related Thiazole Derivatives." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187081.ch4.

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Gujjarappa, Raghuram, Arup K. Kabi, Sattu Sravani, et al. "Overview on Biological Activities of Thiazole Derivatives." In Materials Horizons: From Nature to Nanomaterials. Springer Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-8399-2_5.

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Forti, G. Cantelli, P. Hrelia, M. C. Guerra, M. Paolini, A. M. Barbaro, and G. L. Biagi. "Genotoxic Activity of Nitroimidazo(2,1-b)Thiazole Derivatives in Salmonella Typhimurium and Saccharomyces Cerevisiae Assays." In Archives of Toxicology. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-69928-3_89.

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Dekate, Shital M., Kishor M. Hatzade, and Ajay M. Ghatole. "Design, Synthesis, and Characterization of Some Oxadiazole Derivatives and Their S-Glucosides Bearing Thiazole Scaffold." In Springer Proceedings in Materials. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-5169-3_20.

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Pandey, Anoop Kumar, Ankit Kumar Sharma, Avinash Mishra, Satyendra Nath Tiwari, and Vijay Singh. "Quantum chemical study of thiazole derivative cyclobutyl molecule C18H18N2O3S." In Emerging Trends in IoT and Computing Technologies. Routledge, 2023. http://dx.doi.org/10.1201/9781003350057-54.

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Hegde, Shridhar G., Martin D. Mahoney, and Claude R. Jones. "Thiazolo[4,5-b]pyridine-3(2H)-acetic Acid Derivatives." In ACS Symposium Series. American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0584.ch007.

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Kumar Pandey, Anoop, Ankit Kumar Sharma, V. K. Singh, Benard S. Mwankemwa, and Vijay Singh. "Geometry vibrational and NBO analysis of thiazole derivative (Z)-4-{[4-(3-methyl3-phenylcyclobutyl)thiazol-2-yl]amino}-4-oxobut-2-enoic acid." In Emerging Trends in IoT and Computing Technologies. Routledge, 2023. http://dx.doi.org/10.1201/9781003350057-53.

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Eriks, J. Ch, G. J. Sterk, E. M. van der Aar, S. A. B. E. van Acker, H. van der Goot, and H. Timmerman. "4- or 5-(ω-Aminoalkyl)Thiazoles and Derivatives; New Selective H2-Receptor Agonists." In New Perspectives in Histamine Research. Birkhäuser Basel, 1991. http://dx.doi.org/10.1007/978-3-0348-7309-3_22.

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Singh, Raman, Shivangi Sharma, Shivendra Singh, and Kuldeep Singh. "Thiazole and Thiazolidinone Derivatives as Anti-inflammatory Agents." In Heterocyclic Anti-Inflammatory Agents: A Guide for Medicinal Chemists. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815223460124010008.

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The significant potential of thiazole and thiazolidinone derivatives as antiinflammatory drugs can be observed in their ability to inhibit a variety of inflammatory mediators. These derivatives also inhibit factors that catalyze the synthesis of inflammatory mediators. The anti-inflammatory effects of the derivatives of thiazole and thiazolidinone demonstrated this potential. In addition, they have antioxidant properties that help to reduce oxidative stress and inflammation that the body experiences. These derivatives represent promising molecules for the development of new medications in the
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Conference papers on the topic "Thiazole Derivatives"

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Ghodgaonkar, Sunayana, Jinish Shah, Sachin Laddha, Sandeep Waghulde, and Vaibhav Kulkarni. "Synthesis and Evaluation of Novel Thiazole Derivatives." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00397.

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Thakur, Shabnam, Rupali Sharma, Rakesh Yadav, and Satish Sardana. "The Potential of Thiazole Derivatives as Antimicrobial Agents." In International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13673.

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Saracoglu, Murat, Fatma Kandemirli, Mohammed A. Amin, Can Dogan Vurdu, Muhammet Serdar Cavus, and Gokhan Say ner. "The Quantum Chemical Calculations of Some Thiazole Derivatives." In 3rd International Conference on Computation for Science and Technology (ICCST-3). Atlantis Press, 2015. http://dx.doi.org/10.2991/iccst-15.2015.29.

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Ariza-Rúa, Danilo, Liliana Carranza-López, Edisson Chavarro-Mesa, Julio Hurtado Márquez, and Humberto Marbello-Peña. "2D-QSAR Study of Thiazole derivatives as 5-Lipoxygenase inhibitors." In 22nd LACCEI International Multi-Conference for Engineering, Education and Technology (LACCEI 2024): “Sustainable Engineering for a Diverse, Equitable, and Inclusive Future at the Service of Education, Research, and Industry for a Society 5.0.”. Latin American and Caribbean Consortium of Engineering Institutions, 2024. http://dx.doi.org/10.18687/laccei2024.1.1.1785.

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Kokate, Siddhant V., and Sachin V. Patil. "Synthesis and Antimicrobial Screening of Some New Thiazole Substituted 1,3,4-Oxadiazole Derivatives." In ECSOC-25. MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11662.

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Patil, Sachin V., Manjusha B. Suryavanshi, Deepak R. Nagargoje, and Siddhant V. Kokate. "Synthesis and Antimicrobial Evaluation of Some New Pyrazole Derivatives Containing Thiazole Scaffolds." In ECSOC-25. MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11661.

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Nikhila, G. R., S. R. Batakurki, and B. C. Yallur. "Synthesis, characterization and antioxidant studies of benzo[4, 5]imidazo[2, 1-b]thiazole derivatives." In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON ADVANCES IN MATERIALS RESEARCH (ICAMR - 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0023101.

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Radovanović, Marko, Ignjat Filipović, Maja Đukić, Marija Ristić, Ivan Jakovljević, and Zoran D. Matović. "Molecular docking study of ruthenium-p-cymene complexes with isothiazole derivatives as SARS-CoV-2 main protease inhibitors." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.387r.

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Since proper treatment for COVID-19 still has not been developed, exploration of novel options is required. Activities of different metal complexes, promising results gained from examining different thiazole derivatives, and research in the field of natural products like p-cymene, produced an idea to test piano stool ruthenium p-cymene complexes with isothiazole derivatives as ligands. In silico methods are often used as the first step in a series of experiments during the development of new drugs, and docking simulations are a quick way to determine the feasibility of novel compounds as poten
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jasim, Adel, and Shaimaa Adnan. "Preparation, characterization and study the biological activity for (six and seven) membered heterocyclic derivatives from 6-methoxy-2-amino benzo thiazole." In THE SECOND INTERNATIONAL SCIENTIFIC CONFERENCE (SISC2021): College of Science, Al-Nahrain University. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0118989.

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Ustinov, Ilya, Nikolaj Khlytin, Yurij Atroshchenko, and Irina Shahkeldyan. "NEW THIAZOL DERIVATIVES CONTAINING NITRO QUINOLINE FRAGMENT." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m797.aks-2019/383-384.

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