Relevant bibliographies by topics / Salicylamido

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

Academic literature on the topic 'Salicylamido'

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

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Journal articles on the topic "Salicylamido"

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Malakhova, Anna Yu, and Vladimir N. Kuklin. "Synthesis, the structure of arylsalicylic amides, which have anthelmintic activity." Butlerov Communications 57, no. 3 (2019): 58–70. http://dx.doi.org/10.37952/roi-jbc-01/19-57-3-58.

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Salicylamides (N-aryl-substituted hydroxybenzamides): well-known organic compounds with diverse biological activity, which were originally investigated as antimicrobial and antifungal substances. Salicylamides have also been used as anthelmintic or molluscicidal agents in human and veterinary medicine. The most famous is 5,2'-dichloro-4'-nitrosalicylamide (niclosamide, yomezan – Germany), resynthesized in the USSR under the name of fenasal, which is effective in treating diphyllobothriasis and hymenolepidosis and has molluscicidal properties. The works of domestic and foreign scientists F.S. M
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Makhaeva, Galina F., Nadezhda V. Kovaleva, Elena V. Rudakova, et al. "Conjugates of Tacrine and Salicylic Acid Derivatives as New Promising Multitarget Agents for Alzheimer’s Disease." International Journal of Molecular Sciences 24, no. 3 (2023): 2285. http://dx.doi.org/10.3390/ijms24032285.

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A series of previously synthesized conjugates of tacrine and salicylamide was extended by varying the structure of the salicylamide fragment and using salicylic aldehyde to synthesize salicylimine derivatives. The hybrids exhibited broad-spectrum biological activity. All new conjugates were potent inhibitors of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) with selectivity toward BChE. The structure of the salicylamide moiety exerted little effect on anticholinesterase activity, but AChE inhibition increased with spacer elongation. The most active conjugates were salicylimine de
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Atlasovich, Fabi�n, Jos� A. Santom�, and Horacio N. Fern�ndez. "Photoreactive fatty acid analogues that bind to the rat liver fatty-acid binding protein: 11-(5?-azido-salicylamido)-undecanoic acid derivatives." Molecular and Cellular Biochemistry 120, no. 1 (1993): 15–23. http://dx.doi.org/10.1007/bf00925980.

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Scott, Richard W., Michael J. Costanzo, Katie B. Freeman, et al. "Optimized Fully-Synthetic Salicylamide Heparin Antagonists Have Greater Efficacy Versus LMWHs and Display Improved Hemodynamic Responses as Compared to Protamine." Blood 116, no. 21 (2010): 191. http://dx.doi.org/10.1182/blood.v116.21.191.191.

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Abstract Abstract 191 A series of salicylamides, fully synthetic cationic foldamers designed to disrupt the binding of the pentasaccharide unit of heparin to antithrombin III, were found to be potent neutralizers of the activity of unfractionated heparin (UFH) and low molecular weight heparins (LMWHs). A compound from this series, PMX-60056, is currently in human clinical trials for neutralization of UFH and LMWHs. PMX-60056 potently neutralizes UFH and LMWHs but is not as efficacious versus fondaparinux (FPX). The goal of the present research was to 1) identify back-up compounds to optimize a
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Jesaitis, A. J., G. M. Bokoch, J. O. Tolley, and R. A. Allen. "Lateral segregation of neutrophil chemotactic receptors into actin- and fodrin-rich plasma membrane microdomains depleted in guanyl nucleotide regulatory proteins." Journal of Cell Biology 107, no. 3 (1988): 921–28. http://dx.doi.org/10.1083/jcb.107.3.921.

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Subcellular fractions were prepared from human neutrophils desensitized at 15 degrees C with stimulatory doses of the photoaffinity derivative F-Met-Leu-Phe-N epsilon-(2-(rho-azido[125I]salicylamido)ethyl-1,3'- dithio-propionyl)-Lys. The covalently labeled receptors were found in a membrane fraction of higher density than those from cells preexposed to ligand at 4 degrees C but not desensitized. The denser fraction (rho approximately equal to 1.155 g/cc) was the cellular locus of the membrane associated cytoskeletal proteins, actin, and fodrin, as detected immunologically on western blots. The
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Farat, Oleg, Svetlana Varenichenko, Ekaterina Zaliznaya, and Victor Markov. "REARRANGEMENT OF SUBSTITUTED 1,3-BENZOXAZINES INTO XANTHENE-TYPE COMPOUNDS." Ukrainian Chemistry Journal 86, no. 2 (2020): 111–22. http://dx.doi.org/10.33609/0041-6045.86.2.2020.111-122.

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The rearrangement patterns of new 1,3-benzoxazines derivatives obtained by condensation of substituted salicylamides with cyclic ketones under the influence of Vilsmeier-Haack reagent has been studied. The influence of angel strain in a 4-membered spirocycle prevents the rearrangement of spiro [1,3-benzoxazine-2,1'-cyclobutan]-4(3H)-one under the action of a formylating agent. 1,3-Benzoxazines derivatives with ring sizes from 5- to 8-membered under the action of a formylating agent have formed formylxanthene derivative. Their formation reaction rate depends on the presence of electronegativity
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Pospíšil, Stanislav, Věra Přikrylová, Jan Němeček, and Jaroslav Spížek. "Oxidation and amidation of salicylate by Streptomyces species." Canadian Journal of Microbiology 42, no. 8 (1996): 867–69. http://dx.doi.org/10.1139/m96-111.

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Seven streptomycete strains were tested for biotransformation of salicylate. The products were identified by nuclear magnetic resonance spectroscopy and three types of conversion were found. Streptomyces cinnamonensis and Streptomyces spectabilis formed gentisate and salicylamide concurrently. Streptomyces rimosus transformed salicylate to salicylamide. Streptomyces lividans, Streptomyces coelicolor, Streptomyces griseus and Streptomyces avermitilis produced only gentisate. Time course studies of salicylate conversion by thin-layer chromatography and high pressure liquid chromatography showed
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Abdel-Rahman, Mohamed S., Alluru S. Reddi, Frederick A. Curro, Rita M. Turkall, Abdelrazak M. Kadry, and Julia A. Hansrote. "Bioavailability of aspirin and salicylamide following oral co-administration in human volunteers." Canadian Journal of Physiology and Pharmacology 69, no. 10 (1991): 1436–42. http://dx.doi.org/10.1139/y91-215.

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BC® powder (I) is a commercially available analgesic containing the active ingredients aspirin and salicylamide. The kinetics of I, BC® powder minus aspirin (II), and BC® powder minus salicylamide (III) were evaluated in 13 volunteers. Ten minutes after administration of I, aspirin reached a maximum concentration of 12.9 μg/mL, while salicylamide concentration reached a peak value of 3.4 μg/mL. However, when III was administered, aspirin was not detected at 10 min and only reached a concentration of 0.4 μg/mL at 2 and 6 h. Furthermore, the area under the plasma concentration versus time curve
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Yao, Shu-Feng, Zhao-Sheng Cai, Xu-Juan Huang, and Lan-Xuan Song. "Preparation of Salicylic Nitrile through Direct Catalytic Dehydration of Salicylamide with Immobilized Phosphoric Acid as Catalyst." Asian Journal of Chemistry 32, no. 5 (2020): 1082–86. http://dx.doi.org/10.14233/ajchem.2020.22545.

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Salicylic nitrile was prepared through direct catalytic dehydration of salicylamide under high temperature using immobilized phosphoric acid as catalyst. The catalytic performances of different catalysts were evaluated according to the analytic results of GC-MS, and the feasibility about the preparation of salicylic nitrile by direct catalytic dehydration of salicylamide was investigated according to the composition of product determinated by GC analysis (area nomalization). Experimental results indicated the comprehensive property of silica gel supported phosphoric acid was the best one among
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Zarei, Ali Reza, Abbas Afkhami, and Nahid Sarlak. "Simultaneous Spectrophotometric Determination of Paracetamol and Salicylamide in Human Serum and Pharmaceutical Formulations by a Differential Kinetic Method." Journal of AOAC INTERNATIONAL 88, no. 6 (2005): 1695–701. http://dx.doi.org/10.1093/jaoac/88.6.1695.

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Abstract A rapid, simple, and sensitive differential kinetic method is presented for the determinations of acetaminophen (also known as paracetamol) and salicylamide. The method is based on their oxidation reaction by Fe3+ ion in the presence of 1,10-phenanthroline as indicator. The reactions can be monitored spectrophotometrically by measuring the increase in the absorbance of the solution at 510 nm. Two times were selected one in which only paracetamol is oxidized by Fe3+ ion and the other in which both drugs are oxidized by Fe3+ ion. The data were evaluated by the proportional equations met
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Dissertations / Theses on the topic "Salicylamido"

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Nordström, Fredrik. "Solid-liquid Phase Equilibria and Crystallization of Disubstituted Benzene Derivatives." Doctoral thesis, KTH, Teknisk strömningslära, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4742.

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The Ph.D. project compiled in this thesis has focused on the role of the solvent in solid-liquid phase equilibria and in nucleation kinetics. Six organic substances have been selected as model compounds, viz. ortho-, meta- and para-hydroxybenzoic acid, salicylamide, meta- and para-aminobenzoic acid. The different types of crystal phases of these compounds have been explored, and their respective solid-state properties have been determined experimentally. The solubility of these crystal phases has been determined in various solvents between 10 and 50 oC. The kinetics of nucleation has been inve
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Torrentino-Madamet, Marylin. "Influence des conditions environnementales sur le métabolisme de Plasmodium falciparum." Thesis, Aix-Marseille 2, 2010. http://www.theses.fr/2010AIX20700/document.

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P. falciparum est le principal responsable des formes graves du paludisme. Le parasiteévolue entre deux hôtes (homme et moustique) qui lui imposent différents environnements; ettout particulièrement, des modifications des pressions partielles d’O2 nécessitant des capacitésd’adaptation surprenantes pour un parasite microaérophile. Chez l’hôte vertébré, lesphénomènes de cytoadhésion, ralentissant la progression du parasite notamment au niveau despoumons, augmentent la durée d’exposition aux conditions hyperoxiques.La dynamique de la réponse parasitaire à l’hyperoxie a été étudiée par une approch
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Books on the topic "Salicylamido"

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Magirius, Johannes Erich Florian. Reaktionen von 3-Amino-2H-azirinen mit Salicylhydrazid und Salicylamid: Synthese von Cyclodepsipeptid-Modellen unter Verwendung von 3-Amino-2H-azirinen als Aminosäure-Äquivalente. Zentralstelle der Studentenschaft, 1995.

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Hoffmann, Fred. Über Die Analgetische Potenz Von Acetylsalicylsäure und Salicylamid: Algimetr. Messgn U. Ihre Konsequenz Für D. Praxis; Referat. Springer London, Limited, 2013.

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Book chapters on the topic "Salicylamido"

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Bährle-Rapp, Marina. "Salicylamide." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_9079.

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Beyer, Karl-Heinz. "Salicylamid." In Biotransformation der Arzneimittel. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-74386-3_283.

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Bährle-Rapp, Marina. "Cystamine Bis-Salicylamide." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2610.

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"Salicylamide." In Drugs Handbook 2012–2013. Bloomsbury Academic, 2011. http://dx.doi.org/10.5040/9781350363595.art-1542.

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"Salicylamide." In Hale’s Medications & Mothers’ Milk™ 2019. Springer Publishing Company, 2018. http://dx.doi.org/10.1891/9780826150356.0919.

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Wolkenberg, S. E., and R. M. Garbaccio. "Chiral Salicylamine Catalyzed Strecker Reaction." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00384.

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Wolkenberg, S. E., and R. M. Garbaccio. "Chiral Salicylamine-Based Strecker Synthesis." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00441.

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"AOAC Official Method 972.49Acetaminophen and Salicylamide in Drugs." In Official Methods of Analysis of AOAC INTERNATIONAL, 22nd ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/9780197610145.003.2456.

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Wolkenberg, S. E., and R. M. Garbaccio. "Chiral Salicylamine–Titanium Complex Catalyzed Strecker Synthesis." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00385.

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DEL CAMPILLO, M. CORDERO. "THE EXPERIMENTAL USE OF N-(2′-chlor-4′-nitro-phenyl)-5-chlor-salicylamid AGAINST ECHINOCOCCUS GRANULOSUS." In Proceedings of the First International Congress of Parasitology. Elsevier, 1999. http://dx.doi.org/10.1016/b978-0-08-011427-9.50133-5.

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Conference papers on the topic "Salicylamido"

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Michnová, Hana, Ales Imramovsky, Pratibha Magar, Alois Čížek, and Josef Jampílek. "Antistaphylococcal activity of new salicylamide analogues." In 5th International Electronic Conference on Medicinal Chemistry. MDPI, 2019. http://dx.doi.org/10.3390/ecmc2019-06344.

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