Relevant bibliographies by topics / The compounds have been screened for their fungicidal activity

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Academic literature on the topic 'The compounds have been screened for their fungicidal activity'

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

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Journal articles on the topic "The compounds have been screened for their fungicidal activity"

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Begum, Kahkashan. "Synthesis and Evaluation of Some 2–Aryl–3–[Substituted Pyridin–2–Yl]-Amino/Methylamino Thiazolidin-4-Ones." Oriental Journal of Chemistry 34, no. 6 (2018): 3052–57. http://dx.doi.org/10.13005/ojc/340647.

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A series of compounds incorporating thiazolidinone moiety has been synthesized and screened for their antifungal activity. 2-Aryl-3-[substituted pyridin-2-yl]-amino/methylamino thiazolidin-4-ones have been synthesized by cyclocondensation of [substituted pyridin-2-yl]- araldehydehydrazone and N-Methyl [substituted pyridin-2-yl]-araldehydehydrazone with mercapto acetic acid in dioxane. The initial reactants required for the synthesis were obtained by refluxing 2-hydrazino substituted pyridine and 2-[N-methylhydrazino]-substituted pyridine with different substituted aldehydes. These newly synthe
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Rama Rao, Gurram, Kaleru Mogilaiah, and Bathula Sreenivasulu. "Synthesis of 2-(4-aryl-2-pyrazolin-3-yl)-1,8-naphthyridines by 1,3-dipolar cycloaddition." Collection of Czechoslovak Chemical Communications 54, no. 6 (1989): 1716–20. http://dx.doi.org/10.1135/cccc19891716.

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2-(4-Aryl-2-pyrazolin-3-yl)-1,8-naphthyridines III have been prepared by the cycloaddition of diazomethane to 2-styryl-1,8-naphthyridines II. The structures of the compounds have been confirmed by elemental analyses and spectral data. All these compounds have been screened for fungicidal activity.
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Bao, Longzhu, Shuangshuang Wang, Di Song, Jingjing Wang, Xiali Yue, and Xiufang Cao. "Novel Strobilurin Derivatives Containing Carboxylate Unit as Potential Antifungal Agents." Letters in Drug Design & Discovery 17, no. 3 (2020): 300–311. http://dx.doi.org/10.2174/1570180816666190325164452.

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Background: Due to the extensive use of a single fungicide to control crop diseases, the increase of resistant individuals leads to control failures. The search for molecules with fungicidal activity is still ongoing. Strobilurin is one of the most popularly used fungicides in the agrochemical field. A large number of strobilurin derivatives with both high activity and low toxicity have been developed. Methods: In the present study, a series of novel ortho-substituted benzyl carboxylates were efficiently synthesized by the reaction of (E)-methyl 2-(2-(bromom-ethyl)phenyl)-2-methox-yiminoaceta
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BHARATI, MISHRA, ALI R., and NIZAMUDDIN. "Synthesis and Biological Activities of some 7-Aryl-3-aryli- deneimino-5-thiono- 1 ,4,6,7-tetrahydropyrimido[4,5-d]- imidazol-2-ones." Journal of Indian Chemical Society Vol. 66, Nov 1989 (1989): 813–14. https://doi.org/10.5281/zenodo.6076918.

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Department of Chemistry, University of Gorakhpur, Gorakhpur-273 009 <em>Manuscript received 14 March 1989, accepted 26 June 1989</em> <strong>7-Aryl.-3-ar) lidenelm;no 5-thiono-1,4 6,7-tetrahydropyrimido[4,5 <em>d</em>] imidazol-2-ones (4) have been synthesised by the condensation of 5-arylideno-3-anlideneimino&shy;hydantoins (3) and </strong><strong>thioureas in methanolic sodium hydroxide. The compounds have </strong><strong>been screened for their fungicidal activity</strong> &nbsp;
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BHARATI, MISHRA, ALI R., and NIZAMUDD1N. "Synthesis and Biological Activities of some 7-Aryl-3-aryli- deneimino-5-thiono- 1 ,4,6,7-tetrahydropyrimido[4,5-d]- imidazol-2-ones." Journal of Indian Chemical Society Vol. 66, November 1989 (1989): 813–14. https://doi.org/10.5281/zenodo.6010400.

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Department of Chemistry, University of Gorakhpur, Gorakhpur-273 009 <em>Manuscript received 14 March 1989, accepted 26 June 1989</em> <strong>7-Aryl.-3-ary lidenelmino 5-thiono-1,4 6,7-tetrahydropyrimido[4,5 <em>d</em>] </strong>imidazol-2- <strong>ones (4) have been synthesised by the condensati,n of 5-arylideno-3-anlideneimino&shy;</strong><strong>hydantoins </strong><strong>(3) and </strong><strong>thioureas in methanolic sodium hydroxide. The compounds have </strong><strong>been screened for their fungicidal activity.</strong>
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M., R. CHAURASIA, and K. SHARMA AJAY. "Synthesis of Some New 4(3H)Quinazolinones as CNS Depressants and Antifungal Agents." Journal of Indian Chemical Society Vol. 62, Apr 1985 (1985): 308–9. https://doi.org/10.5281/zenodo.6324777.

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Department of Chemistry, D.A.V. (P.G ) College, Dehra Dun-248 001 <em>Manuscript received 17 June 1983, revised 3 July 1984, accepted 27 April 1985</em> Several new 6,8-dichloro-2-phenyl-3[(substituted)benzothiazol-2&#39;-yl]-4(3<em>H</em>)quinazo&shy;linoces have been synthesised and screened for their CNS depressant activity. Their fungicidal activity has also been screened on <em>Aspergillus niger </em>and <em>Alternarta alternata </em>at two dilutions. The antifungal screening of compounds reveals that some of them inhibit fungal growth.
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Chary, Maringanti Thirumala, Kaleru Mogilaiah, and Bathula Sreenivasulu. "Synthesis of 2-methyl-3-(5-phenyl or 1,5-diphenyl-2-pyrazolin-3-yl)-1,8-naphthyridines." Collection of Czechoslovak Chemical Communications 53, no. 7 (1988): 1543–48. http://dx.doi.org/10.1135/cccc19881543.

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3-Cinnamoyl-2-methyl-1,8-naphthyridines II have been synthesized utilizing Claisen-Schmidt condensation of 3-acetyl-2-methyl-1,8-naphthyridine I with aromatic aldehydes. The cinnamoyl naphthyridines react with hydrazine hydrate and phenylhydrazine to create the corresponding pyrazolinyl 1,8-naphthyridine derivatives (III and IV). The structures II-IV have been confirmed by their elemental analyses and spectral data. Some of the compounds have been screened for their fungicidal activity.
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BHARATI, MISHRA, ALI R., and NIZAMUDDIN. "Synthesis and Biological Activities of some 7-Aryl-3-arylideneimino-5-thiono- 1,4,6, 7 -tetrahydropyrimido[ 4,5-d]- imidazol-2-ones." Journal of Indian Chemical Society Vol. 66, Nov 1989 (1989): 813–14. https://doi.org/10.5281/zenodo.6106281.

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Department of Chemistry, University of Gorakhpur, Gorakhpur-273 009 <em>Manuscript received 14 March 1989, accepted 26 June 1989</em> 7-Aryl-3-arylideneimino 5-thiono-1,4 6, 7-tetrahydropyrimido[4,5 <em>d</em>]imidazol-2- ones (4) have been synthesised by the condensati,n of 5-arylideno-3-arylideneminohydantoins (3) and thioureas in methanolic sodium hydroxide. The compounds have been screened for their fungicidal activity
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BANDANA, DWIVEDI, TIWARI NIRUPAMA, and NIZAMUDDIN. "Synthesis of some 1-Aroyl-3-methyl-4-substituted phenyl-6-imino-4,7 -dihydro-1 ,3-thiazino[5,4-d]pyrazoles as Pesticides." Journal of Indian Chemical Society Vol. 68, Sep 1991 (1991): 515–16. https://doi.org/10.5281/zenodo.5970875.

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Department of Chemistry, University of Gorakhpur, Gorakhpur-273 009 <em>Manuscript received 24 January 1991, revised 9 August 1991, accepted 3 September 1991</em> 1-Aroyl-3-methyl-4-substituted-phenyl-6-imino-4,7-dihydro-1, 3-thiazino [5. 4-<em>d</em>]-pyrazoles (3) have been synthesised by the condensation of 1-aroyl-4-aryledino-3- methyl-5-pyrazolones (2) and thiourea in methanolic potassium hydroxide. The compounds have been screened for their fungicidal activities against<em> A. niger</em> and <em>A. flavus</em> and antibacterial activities against <em>S.</em> <em>aureus</em> and <em>B.</e
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Gaman, Barat* Navin Patel. "SYNTHESIS AND IN VITRO PHARMACOLOGICAL STUDIES OF SOME NOVEL PRECURSORS OF 6, 8-DIBROMOQUINAZOLIN-4(3H) ONE." INTERNATIONAL JOURNAL OF ENGINEERING SCIENCES & RESEARCH TECHNOLOGY 5, no. 12 (2016): 465–72. https://doi.org/10.5281/zenodo.203855.

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A novel series of some precursors of 6, 8-dibromoquinazolin-4(3H)-one 61-12 have been synthesized by the based catalysed cyclisation of chromenamido 51-12 with phenylhydrazine hydrate. The overall reaction was base catalysed conventional multistep process. The title compounds have been confirmed by spectral data IR, 1H NMR, 13C NMR and elemental analysis. All the synthesized target molecules were screened for gram positive, gram negative antibacterial and fungicidal activity In Vitro by disc diffusion method. The zone of inhibition measured and calculated potency. The pharmacological strength
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Book chapters on the topic "The compounds have been screened for their fungicidal activity"

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Rizvi, Fahmina, Mohsin Ali Khan, Mohammad Saquib, and Mohammad Faheem Khan. "Butea monosperma: Phytochemistry and Pharmacological Applications." In Metabolites of Medicinal Plants: Insightful Approaches. BENTHAM SCIENCE PUBLISHERS, 2024. https://doi.org/10.2174/9789815274103124010008.

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Butea monosperma, also known as the 'Flame of the forest' or 'Palas' in Hindi, belongs to the important medicinal plant family “Fabaceae.” Its endemic presence in Southeast Asia and India has made it a valuable natural resource. This plant has a variety of medicinal applications, such as being an aphrodisiac, antiinflammatory, anthelmintic, antimicrobial, and many more. The presence of flavonoids, triterpenes, steroids, chalcones, and fatty acids in different parts of B. monosperma, including the stem, root, leaves, and flowers, makes it a versatile ingredient in various therapeutic exercises.
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Slimani, Ichraf, Khaireddine Dridi, Ismail Özdemir, Nevin Gürbüz, and Naceur Hamdi. "Novel N-Heterocyclic Carbene Silver (I) Complexes: Synthesis, Structural Characterization, Antimicrobial, Antioxidant and Cytotoxicity Potential Studies." In Carbene. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.101950.

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Nowadays, N-heterocyclic carbene-based silver-complexes Ag(I) have been widely used as an organometallic drug candidate in medicinal and pharmaceutical chemistry researches due to their low toxicity. Due to the success of Ag(I) complexes in biological applications, interest in the synthesis and applications of such compounds is increasing rapidly. Therefore, in this study, a series of unsymmetrical N,N-disubstituted benzimidazolium salts were synthesized as N-heterocyclic carbene (NHC) (2a-2j). The interaction of these benzimidazolium salts having their two nitrogen atoms substituted by bulky
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Shreeya, Tejal, and Tabish Qidwai. "High Throughput Screening (HTS) Methods for Screening of Known Drugs for COVID-19." In Drug Repurposing Against SARS-CoV-2. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815123197123010009.

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The emergence of severe acute respiratory syndrome coronavirus 2 (SARS.CoV-2) in late 2019 has triggered an ongoing global pandemic whereby infection may result in a lethal severe pneumonia-like disease designated as coronavirus disease 2019 (COVID-19). Thus, the repositioning of known drugs can significantly accelerate the development and deployment of therapies for COVID-19. High throughput screening (HTS) is the use of automated equipment to rapidly test thousands to millions of samples for biological activity at the model organism, cellular, pathway, or molecular level. In its most common
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Satapathy, Swapnashree, Ananya Kuanar, and Arun Kumar Pradhan. "Application of Biosurfactant in Agriculture." In Biosurfactants: A Boon to Healthcare, Agriculture & Environmental Sustainability. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815196924124010007.

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All countries are concerned about meeting the growing demands of the human population in terms of agricultural output in a timely manner. Biosurfactants are substances that bacteria, yeasts and fungus are said to create as green surfactants which are less harmful and environmentally compassionate. Several forms of biosurfactants could be commercialised for use in the pharmaceutical, cosmetics, and food industries. Surface active molecules are frequently utilised in agricultural soil remediation to improve soil quality. In recent years, the chemical compounds have gotten a lot of attention beca
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Conference papers on the topic "The compounds have been screened for their fungicidal activity"

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Kharshan, Margarita, Kristy Gillette, Alla Furman, Robert Kean, and Liz Austin. "Novel Corrosion Inhibitors Derived from Agricultural by-Products: Potential Applications in Water Treatment." In CORROSION 2012. NACE International, 2012. https://doi.org/10.5006/c2012-01154.

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Abstract The corrosion inhibitive properties of biodegradable, and non-hazardous corn-based by-products were evaluated and screened to identify potential applications. The properties evaluated included contact- and vapor-phase corrosion inhibition, as well as the ability to act as a barrier against corrosive environments such as high acid concentration and salt solutions. Rust and scale removing properties were also tested. During these investigations, it was discovered that a solvent extract from dried distilled grains with solubles (DDGS) demonstrated very good corrosion protection propertie
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Todorović, Jovana D., Aleksandra D. Vesić, Nevena N. Petrović, and Marijana M. Kosanić. "Edible mushrooms as promising antioxidants." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.300t.

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Antioxidant activity of the acetone extracts of the mushrooms Macrolepiota procera and Chlorophyllum rhacodes has been screened in vitro by using different methods (DPPH radical scavenging and reducing power assay), and also it has been determined the total phenolic compounds as total flavonoid content. The research findings indicate that the acetone extract of M. procera demonstrated superior antioxidant activities when compared to C. rhacodes. Similarly, the mushroom M. procera displayed a more pronounced effect on reducing power. In addition, the total content of phenol and flavonoid in ext
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