Relevant bibliographies by topics / Phenylhydrazides

Contents

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

Academic literature on the topic 'Phenylhydrazides'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Phenylhydrazides"

1

Knizek, Jörg, Ingo Krossing, Heinrich Nöth, Holger Schwenk, and Thomas Seifert. "Synthesis and Structures of Sodium Phenylhydrazides." Chemische Berichte 130, no. 8 (1997): 1053–62. http://dx.doi.org/10.1002/cber.19971300806.

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do Carmo Maquiaveli, Claudia, Edson Roberto da Silva, Barbara Hild de Jesus, et al. "Design and Synthesis of New Anthranyl Phenylhydrazides: Antileishmanial Activity and Structure–Activity Relationship." Pharmaceuticals 16, no. 8 (2023): 1120. http://dx.doi.org/10.3390/ph16081120.

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Leishmaniasis is a neglected tropical disease affecting millions of people worldwide. A centenary approach to antimonial-based drugs was first initiated with the synthesis of urea stibamine by Upendranath Brahmachari in 1922. The need for new drug development led to resistance toward antimoniates. New drug development to treat leishmaniasis is urgently needed. In this way, searching for new substances with antileishmanial activity, we synthesized ten anthranyl phenylhydrazide and three quinazolinone derivatives and evaluated them against promastigotes and the intracellular amastigotes of Leish
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Čeřovský, Václav, та Karel Jošt. "Enzymatically catalyzed synthesis of dipeptides of γ-carboxy-L-glutamic acid from benzyloxycarbonyl-γ-carboxy-DL-glutamic acid". Collection of Czechoslovak Chemical Communications 50, № 4 (1985): 878–84. http://dx.doi.org/10.1135/cccc19850878.

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Enantioselective reaction of benzyloxycarbonyl-γ-carboxy-DL-glutamic acid with phenylhydrazides of various amino acids and with leucine, protected with various carboxy-protecting groups, has been studied.
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Zhu, Panpan, Jinshuo Zheng, Jin Yan, Zhaoxia Li, Xinyi Li, and Huiling Geng. "Design, Synthesis, and Biological Evaluation of N′-Phenylhydrazides as Potential Antifungal Agents." International Journal of Molecular Sciences 24, no. 20 (2023): 15120. http://dx.doi.org/10.3390/ijms242015120.

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Fifty-two kinds of N′-phenylhydrazides were successfully designed and synthesized. Their antifungal activity in vitro against five strains of C. albicans (Candida albicans) was evaluated. All prepared compounds showed varying degrees of antifungal activity against C. albicans and their MIC80 (the concentration of tested compounds when their inhibition rate was at 80%), TAI (total activity index), and TSI (total susceptibility index) were calculated. The inhibitory activities of 27/52 compounds against fluconazole-resistant fungi C. albicans 4395 and 5272 were much better than those of fluconaz
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GEMUEND, B., H. NOETH, H. SACHDEV, and M. SCHMIDT. "ChemInform Abstract: Structural Chemistry of Alkali Metal Phenylhydrazides." ChemInform 28, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199706081.

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Gąsowska, Beata, Bożena Frąckowiak, and Hubert Wojtasek. "Indirect oxidation of amino acid phenylhydrazides by mushroom tyrosinase." Biochimica et Biophysica Acta (BBA) - General Subjects 1760, no. 9 (2006): 1373–79. http://dx.doi.org/10.1016/j.bbagen.2006.05.001.

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Verardo, Giancarlo, Paola Geatti, Paolo Martinuzzi, Marcello Merli та Nicoletta Toniutti. "Condensation Reaction Betweenα-Amino Acid Phenylhydrazides and Carbonyl Compounds". European Journal of Organic Chemistry 2003, № 19 (2003): 3840–49. http://dx.doi.org/10.1002/ejoc.200300251.

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Crizanto de Lima, Evanoel, Frederico S. Castelo-Branco, Claudia C. Maquiaveli, et al. "Phenylhydrazides as inhibitors of Leishmania amazonensis arginase and antileishmanial activity." Bioorganic & Medicinal Chemistry 27, no. 17 (2019): 3853–59. http://dx.doi.org/10.1016/j.bmc.2019.07.022.

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Čeřovský, Václav, and Karel Jošt. "Enzymatically catalyzed synthesis of oxytocin fragments 1-6 and 7-9." Collection of Czechoslovak Chemical Communications 50, no. 12 (1985): 2775–82. http://dx.doi.org/10.1135/cccc19852775.

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Papain, α-chymotrypsin, thermolysin and elastase were utilized in the synthesis of peptide bonds of the protected oxytocin nonapeptide, except the S-benzylcysteine-proline bond. Amino groups were protected with benzyloxycarbonyl or tert-butyloxycarbonyl groups, carboxy groups as ethyl ester, phenylhydrazides or amides. The cysteine sulfhydryl group was blocked with the benzyl group whereas the tyrosine hydroxyl was unprotected. Most of the fragments were synthesized in satisfactory yields using an equimolar ratio of both reaction components and minimal (experimentally determined) amount of the
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Čeřovský, Václav. "Synthesis of pressinoic acid by enzymatically catalyzed formation of peptide bonds." Collection of Czechoslovak Chemical Communications 51, no. 6 (1986): 1352–60. http://dx.doi.org/10.1135/cccc19861352.

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Three fully enzymatic syntheses of the 1-6 vasopressin hexapeptide were investigated using papain, α-chymotrypsin and thermolysin. Best results were obtained with thermolysin in the 2 + 4 fragment condensation. The α-chymotrypsin-catalyzed 3 + 3 condensation is less advantageous and the 4 + 2 condensation with papain gave only low yield. Using the mentioned enzymes, further fragments of vasopressin molecule were prepared. Amino groups were protected with benzoylcarbonyl or tert-butyloxycarbonyl groups, carboxyl groups as phenylhydrazides or methyl esters, and the cysteine sulfhydryl group as t
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Dissertations / Theses on the topic "Phenylhydrazides"

1

Alshabanah, Othman A. "Polyamine and acetylpolyamine levels during phenylhydrazine-induced erythropoiesis in mouse spleen." Scholarly Commons, 1988. https://scholarlycommons.pacific.edu/uop_etds/3406.

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The phenylhydrazine-induced erythropoietic mouse spleen is used as a model system to demonstrate the relationship between tissue growth and polyamine metabolism. Phenylhydrazine produced significant changes in spleen weights, hematocrits and reticulocyte counts in Swiss-Webster mice. The average spleen weight went up from a control of 155 mg to 875 mg at 96 hours after phenylhydrazine administration, while a 49% reduction in the value of hematocrit was observed at 72 hours. Reticulocyte counts in peripheral blood went from 0.8 to 58% at 168 hours after treatment with phenylhydrazine. Phenylhyd
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Іншина, Наталія Миколаївна, Наталия Николаевна Иншина, Nataliia Mykolaivna Inshyna та Я. А. Гриценко. "Роль біосинтезу гему в регуляції вмісту цитохрому р-450 за умов фенілгідразинової анемії". Thesis, Сумський державний університет, 2017. http://essuir.sumdu.edu.ua/handle/123456789/55073.

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Як відомо, фенілгідразін є класичним гемолітичним агентом. Метаболізм фенілгідразину здійснюється в печінці за участю цитохрома Р-450 (цх Р-450). В гепатоцитах 70 % гему, синтезованого de novo, використовується для утворення цх Р-450. Регуляторним ферментом біосинтезу гему є 5-амінолевулінатсинтаза (5-АЛК-синтаза).
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Marsella, Adam Manuele. "A new method for the measurement of airborne formaldehyde using derivatization with 3,5-bis(trifluoromethyl)phenylhydrazine." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0019/MQ45914.pdf.

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Hoang, Jane Vu. "Inactivation of Choline Oxidase by Irreversible Inhibitors or Storage Conditions." Digital Archive @ GSU, 2006. http://digitalarchive.gsu.edu/chemistry_theses/4.

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Choline oxidase from Arthrobacter globiformis is a flavin-dependent enzyme that catalyzes the oxidation of choline to betaine aldehyde through two sequential hydride-transfer steps. The study of this enzyme is of importance to the understanding of glycine betaine biosynthesis found in pathogenic bacterial or economic relevant crop plants as a response to temperature and salt stress in adverse environment. In this study, chemical modification of choline oxidase using two irreversible inhibitors, tetranitromethane and phenylhydrazine, was performed in order to gain insights into the active sit
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EL, HAMDAOUI AZEDDINE. "Degradation du caoutchouc par oxydation controlee. Action du couple phenylhydrazine/oxygene sur des cetones modeles des extremites de chaine." Le Mans, 1991. http://www.theses.fr/1991LEMA1011.

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L'objectif du travail realise est l'identification des extremites de chaine obtenues apres degradation controlee du caoutchouc naturel en phase latex sous l'action du couple phenylhydrazine/oxygene. Le but de la these est de verifier l'hypothese anterieure de transformation des extremites methyl- et phenylcetone en extremites phenylhydrazone puis -(phenylazo)hydroperoxyde par utilisation de molecules modeles de ces extremites fonctionnelles. Le chapitre bibliographique permet d'une part, de mettre en evidence les apports du travail presente par rapport aux connaissances anterieures, et d'autre
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CHALLIOUI, GILLET CAROLE. "Degradation du caoutchouc naturel en phase latex par oxydation controlee. Action du couple phenylhydrazine/oxygene sur un modele des structures polyisopreniques." Le Mans, 1994. http://www.theses.fr/1994LEMA1024.

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Ce memoire traite de l'etude de la degradation controlee du caoutchouc naturel en phase latex sous l'action du couple redox phenylhydrazine/oxygene. En se basant sur les resultats des travaux anterieurs et possedant a present, des methodes d'analyses plus performantes (rmn #1h 400mhz et cg/sm), notre travail a consiste a identifier de maniere plus sure et plus complete les fonctions d'extremites de chaine apres degradation. Pour cela, nous avons cherche dans un premier temps a alimenter notre reflexion en completant nos connaissances des processus d'oxydation et de degradation du polyisoprene
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Mashregi, Mariam. "Accelerated cytotoxic mechanism screening of isoniazid and phenylhydrazine using an in vitro hepatocyte inflammation model." 2006. http://link.library.utoronto.ca/eir/EIRdetail.cfm?Resources__ID=450629&T=F.

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Farhat, Fatima. "Développement de méthodes analytiques de séparation des produits de digestion enzymatique des dérivés de cellulose." Thèse, 2009. http://hdl.handle.net/1866/3910.

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La cellulose et ses dérivés sont utilisés dans un vaste nombre d’applications incluant le domaine pharmaceutique pour la fabrication de médicaments en tant qu’excipient. Différents dérivés cellulosiques tels que le carboxyméthylcellulose (CMC) et l’hydroxyéthylcellulose (HEC) sont disponibles sur le commerce. Le degré de polymérisation et de modification diffèrent énormément d’un fournisseur à l’autre tout dépendamment de l’origine de la cellulose et de leur procédé de dérivation, leur conférant ainsi différentes propriétés physico-chimiques qui leurs sont propres, telles que la viscosité et
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Books on the topic "Phenylhydrazides"

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R, Cary, Dobson S, Brooke I, et al., eds. Phenylhydrazine. World Health Organization, 2000.

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I, Brooke, and Great Britain. Health and Safety Executive., eds. Phenylhydrazine: Risk assessment document EH72/1. HSE Books, 1997.

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Marsella, Adam Manuele. A new method for the measurement of airborne formaldehyde using derivatization with 3,5-bis(trifluoromethyl)phenylhydrazine. National Library of Canada, 1999.

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Phenylhydrazine. World Health Organization, 2000.

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executive, Health and safety. Phenylhydrazine. Health and Safety Executive (HSE), 1997.

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Mashregi, Mariam. Accelerated cytotoxic mechanism screening of isoniazid and phenylhydrazine using an in vitro hepatocyte inflammation model. 2006.

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Book chapters on the topic "Phenylhydrazides"

1

Holze, Rudolf. "Ionic conductivities of phenylhydrazine." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_226.

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Lattová, Erika, and Hélène Perreault. "Method for Investigation of Oligosaccharides Using Phenylhydrazine Derivatization." In Glycomics. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-022-5_5.

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Arduini, A., J. Dejulia, V. Damonti, et al. "The Effect of Phenylhydrazine on the Membrane Phospholipid Organization." In Fluorescent Biomolecules. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-5619-6_45.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) complex with N-salicylidene phenylhydrazine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_291.

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Chen, Z., and A. Stern. "Effects of Phenylhydrazine on Human Red Cell Membrane Aminophospholipids: A Fluorescamine Study." In Prostaglandin and Lipid Metabolism in Radiation Injury. Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-5457-4_9.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear chromium(II) complex with acetate and phenylhydrazine ligands." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_226.

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Semenov, Anatoly N., Irina V. Lomonosova, and Mikhail I. Titov. "Copper (II) complexes as catalysts for oxidative removal of the phenylhydrazide protecting group under mild conditions." In Peptides 1992. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1470-7_81.

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Comporti, M., C. Signorini, L. Sugherini, A. Pompella, L. Ciccoli, and M. Ferrali. "Hepatic Iron Overload Induced by Phenylhydrazine: Release of Iron in a Free Form and DNA Damage." In New Trends in Hepatology. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0357-9_7.

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Horn, Sara, Nava Bashan, Shimon Moses, and Jacob Gopas. "Phagocytosis of Phenylhydrazine Oxidized and G-6-PD Deficient Red Blood Cells: The Role of Sugars and Cell-Bound Immunoglobulins." In Advances in Experimental Medicine and Biology. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4684-5985-2_26.

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Pokhrel, Prabhat K., and Cesar A. Lau-Cam. "In Vitro and In Vivo Effects of Taurine and Structurally Related Sulfur-Containing Compounds Against Phenylhydrazine-Induced Oxidative Damage to Erythrocytes." In Advances in Experimental Medicine and Biology. Springer US, 2002. http://dx.doi.org/10.1007/0-306-46838-7_56.

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Conference papers on the topic "Phenylhydrazides"

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Franconetti, Antonio, Manuel Gómez-Guillén, Pastora Borrachero, and Francisca Cabrera-Escribano. "Structural studies of phenylhydrazine integration in carbohydrate derivatives." In The 15th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00693.

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Atanasković, Ana, Thomas Eichhorn, Dejan Milenković, Dušan Dimić, Goran Kaluđerović, and Jasmina Dimitrić Marković. "Synthesis, spectroscopic, and theoretical analysis of Ru(II)-phenylhydrazine complex." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.395a.

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In recent decades, metal-based chemotherapeutics have attracted considerable attention and excitement within the oncology research community, with ruthenium(II) complexes emerging as a particularly promising class of anticancer agents. In this study, the synthesis of a new ruthenium complex was performed, followed by its structural characterization using NMR and IC spectroscopy. The compound’s infrared spectrum reveals characteristic bands corresponding to N-H and C-H stretching vibrations from sp2 and sp3 hybridized carbon atoms, vibrations of aromatic rings and additional vibrations related
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Soubhye, Jalal. "Dual Anti-Inflammatory and Anti-Bacterial Effects of Phenylhydrazide and Phenylhydrazone Derivatives." In 3rd International Electronic Conference on Medicinal Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecmc-3-04699.

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Busroni, Busroni, Ari Tri Wanodyo Handayani, Eka Deddy Irawan, and Chairil Anwar. "Synthesis and characterization of novel basketing of C-4-phenylocta-phenylhydrazide-calix[4]resorcinarene-PdNPs." In VIII INTERNATIONAL ANNUAL CONFERENCE “INDUSTRIAL TECHNOLOGIES AND ENGINEERING” (ICITE 2021). AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0111699.

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Fauzi’ah, Lina, and Tutik Dwi Wahyuningsih. "Cyclization reaction of 4-nitro-3’-4’-dimethoxychalcone and phenylhydrazine as antibacterial candidate." In 2ND INTERNATIONAL CONFERENCE ON CHEMISTRY, CHEMICAL PROCESS AND ENGINEERING (IC3PE). Author(s), 2018. http://dx.doi.org/10.1063/1.5065021.

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Jasril, J., I. Ikhtiarudin, Y. Nurulita, and Nurisma. "Microwave-assisted synthesis and antioxidant activity of an imine, (E)-1-(3-bromobenzylidene)-2-phenylhydrazine." In PROCEEDINGS OF THE 5TH INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES (ISCPMS2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0009374.

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Jasril, Yuana Nurulita, Nur Afriana, Ihsan Ikhtiarudin, and Neni Frimayanti. "Microwave-assisted synthesis and antioxidant activity of a hydrazone, (E)-1-(4-methoxybenzylidene)-2- phenylhydrazine." In THE 2ND SCIENCE AND MATHEMATICS INTERNATIONAL CONFERENCE (SMIC 2020): Transforming Research and Education of Science and Mathematics in the Digital Age. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0042010.

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Gonzales, J., W. Chen, Y. Epshtein, C. Humpal, J. Chen, and D. R. Fraidenburg. "Murine Model of Phenylhydrazine-Induced Chronic Hemolysis Combined With Hypoxia Leads to Development of Severe Pulmonary Hypertension." In American Thoracic Society 2023 International Conference, May 19-24, 2023 - Washington, DC. American Thoracic Society, 2023. http://dx.doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a4660.

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Al-Yasari, Ali Mosa Rashid, Mohammed A. Aboktifa, Zainab Abdulkaleq Ahmed, Hadeel S. Almaliki, Ruqaya K. Abbas, and Adnan Mansour Jasim. "The physiological role of phytosomal curcumin to mitigate hemolytic anemia and cytogenic effect induced by phenylhydrazine in rats." In TRANSPORT, ECOLOGY, SUSTAINABLE DEVELOPMENT: EKO VARNA 2023. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0191865.

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Marsella, A., J. Purdham, and S. Mabury. "389. Development and Application of a New Method for the Measurement of Airborne Formaldehyde Using Solid Phase Derivatization With 3,5-Bis (Trifluoromethyl)Phenylhydrazine." In AIHce 1999. AIHA, 1999. http://dx.doi.org/10.3320/1.2763246.

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Reports on the topic "Phenylhydrazides"

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NIOSH skin notation (SK) profiles: phenylhydrazine [CAS No. 100-63-0]. U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 2014. http://dx.doi.org/10.26616/nioshpub2014147.

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