Relevant bibliographies by topics / Amino-pyrimidines and Antimicrobial activity

Contents

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

Academic literature on the topic 'Amino-pyrimidines and Antimicrobial activity'

Author: Grafiati
Published: 4 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Amino-pyrimidines and Antimicrobial activity"

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KHADIGA, M. GHONBIM, EL-TELBANY FARAG, and YOUSSEF KHAIRIA. "Synthesis and Evaluation of some 2-, 4- and 2,4- Di-substituted.-6-methylpyrimidine Derivatives for Antimicrobial Activity." Journal of Indian Chemical Society Vol. 63, Oct 1986 (1986): 914–17. https://doi.org/10.5281/zenodo.6302313.

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Organic Chemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt <em>Manuscript received</em> <em>23 September 1986, accepted 2 August 1986</em> The reaction of 2-amino-4-cbloro-, 4-amino-2-chloro- and 2,4-dichloro-6-methyl&shy;pyrimidines with primary aromatic amines under acidic conditions is presented. 2-,&nbsp;and 4-<sup>\(\omega\)</sup>-substituted-thioureido-6-methylpyrimidines were synthesised via the reaction of 2-amino-and 4-amino-6-metbylpyrimidine derivatives with arylisocyanates. Six com&shy;pounds were evaluated for their antimicrobial activity and most of them sh
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R., S. Dhivare, and S. Rajput S. "Microwave Assisted Synthesis and Microbial Screening of Novel Amino-pyrimidine Derivatives using Bis-chalcones." Journal of Chemistry and Chemical Sciences (An International Research Journal), www.chemistry-journal.org 5, no. 10 (2015): 550–56. https://doi.org/10.5281/zenodo.3909691.

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ABSTRACT A simple and clean one pot method for the preparation of amino-pyrimidine derivatives using chalcones of cyclic imides and guanidine nitrate in presence of neutral alumina under microwave supported solvent free condition is described. Some of the synthesized amino-pyrimidines showed synergistic significant activities against Candida albicans and Aspergillus niger fungal strains.
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R., S. Dhivare, and S. Rajput S. "Microwave assisted synthesis and antimicrobial screening of novel 9-(N-phenyl) - 4, 5-(2″, ‴- methoxyphenol)-9H-1,3,6,8,9-hexa-azo-fluorene-2,7- diamine derivatives using bis-heterocyclic chalcones." INTERNATIONAL JOURNAL OF ADVANCES IN PHARMACY, BIOLOGY AND CHEMISTRY 4, no. 4 (2015): 863–70. https://doi.org/10.5281/zenodo.3909811.

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<strong>ABSTRACT</strong> Amino-pyrimidine derivatives were synthesized by a simple and clean single pot method using bis-chalcones of different substituted phenyl glutarimides and guanidine nitrate with neutral alumina irradiated under the microwave supported solvent less condition is demonstrated. All the compounds were screened for their antimicrobial activities and showed moderate activities. But certain amino-pyrimidines exhibited synergistic and significant activities against <em>Candida albicans</em> and <em>Aspergillus niger</em> fungal genres.
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Mohamed, Mosaad, Ramdan El-Domany, and Rania Abd El-Hameed. "Synthesis of certain pyrrole derivatives as antimicro-bial agents." Acta Pharmaceutica 59, no. 2 (2009): 145–58. http://dx.doi.org/10.2478/v10007-009-0016-9.

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Synthesis of certain pyrrole derivatives as antimicro-bial agentsIn an effort to establish new pyrroles and pyrrolo[2,3-d] pyrimidines with improved antimicrobial activity we report here the synthesis andin vitromicrobiological evaluation of a series of pyrrole derivatives. A series of new 2-aminopyrrole-3-carbonitriles (1a-d) were synthesized from the reaction of benzoin, primary aromatic amines and malononitrile, from which a number of pyrrole derivatives (2a-dto5a-d) and pyrrolo[2,3-d]pyrimidines (6a-dto10a, d) were synthesized. Thein vitroantimicrobial testing of the synthesized compounds
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Hossain, M. I., and M. M. H. Bhuiyan. "Synthesis and Antimicrobial Activities of Some New Thieno and Furopyrimidine Derivatives." Journal of Scientific Research 1, no. 2 (2009): 317–25. http://dx.doi.org/10.3329/jsr.v1i2.2299.

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Fused pyrimidines, 8,9-dimethyl[1,2,4]triazolo[4,3-c]thieno[3,2-e]pyrimidine 5, 3,8,9-trimethyl[1,2,4]triazolo[4,3-c]thieno[3,2-e]pyrimidine 6, 4-benzylidinehydrazono-5,6 dimethylthieno[2,3-d]pyrimidine 7, 4-[4/-hydroxybenzylidine]hydrazono-5,6-dimethylthi-eno[2,3-d]pyrimidine 8, 4-[4/-tolylidin]hydrazono-5,6-dimethylthieno[2,3-d]pyrimidine 9, 4-[4/-nitrobenzylidine]hydrazono-5-ethyl-6-methylthieno[2,3-d]pyrimidine 10 and 4-[4/-chlorobenzylidine]hydrazono-5-ethyl-6-methylthieno[2,3-d]pyrimidine 11 are prepared in good yield by an initial treatment of 2-amino-4,5-dimethylthiophene-3-carbonitril
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Vaghasia, S. J., and V. H. Shah. "Microwave assisted synthesis and antimicrobial activity of some novel pyrimidine derivatives." Journal of the Serbian Chemical Society 72, no. 2 (2007): 109–17. http://dx.doi.org/10.2298/jsc0702109v.

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The synthesis of thiazolo[5,4-d]pyrimidines can be achieved from different 5- thiazolidinones, 2-butyl-1H-imidazole-5-carbaldehyde and thiourea using microwave irradiation within 5 min. The structures of the products were supported by FTIR, PMR and mass spectral data. The in vitro antimicrobial activity of the synthesized thiazolo[5,4-d]pyrimidines 1a-j, having substituents at the 1- and 3-positions, were determined by the cup-plate method against several standard strains chosen to define the spectrum and potency of the new compounds. The antimicrobial activities of the thiazolo[5,4-d]pyrimidi
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Butta, Ragavendra, Sowmya Donthamsetty V, Padmaja Adivireddy, and Padmavathi Venkatapuram. "Synthesis and Antimicrobial Activity of Azolyl Pyrimidines." Journal of Heterocyclic Chemistry 54, no. 1 (2016): 524–30. http://dx.doi.org/10.1002/jhet.2615.

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Mohamed, Mounir A. A., Adnan A. Bekhit, Omyma A. Abd Allah, et al. "Synthesis and antimicrobial activity of some novel 1,2-dihydro-[1,2,4]triazolo[1,5-a]pyrimidines bearing amino acid moiety." RSC Advances 11, no. 5 (2021): 2905–16. http://dx.doi.org/10.1039/d0ra08189b.

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Yadav, Bodke, and S. Sangapure S. "Synthesis and biological activity of some benzofuro[3,2-d]pyrimidines." Journal of Indian Chemical Society Vol. 80, Mar 2003 (2003): 187–89. https://doi.org/10.5281/zenodo.5839259.

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Department of Studies and Research in Chemistry. Gulbarga University, Gulbarga-585 106, India <em>E-mail :</em> bodke___yd@rediffmail.com <em>Manuscript received 21 December 2001 .revised 18 April 2002, accepted 12 December 2002</em> The condensation of ethyl 3-amino-2-benzofuran carboxylate (1) with phenyl isocyanate gave 3-phenylureido-2-benzofuran carboxylate (2), which upon treatment&nbsp;with phosphorus oxychloride gave 2-chloro-3-phenyl-3,4-dihydro-4-oxohenzofnro[3,2-<em>d</em>]pyrimidine (4). The reaction of 4 with alicyclic amines like piperidine and morpholine yielded 2-piperidino/mor
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Gomha, Sobhi, Ikhlass Abbas, Mohamed Elneairy, Mahmoud Elaasser, and Bazada Mabrouk. "Antimicrobial and anticancer evaluation of a novel synthetic tetracyclic system obtained by Dimroth rearrangement." Journal of the Serbian Chemical Society 80, no. 10 (2015): 1251–64. http://dx.doi.org/10.2298/jsc141222022g.

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A series of pyrido[3',2':4,5]thieno[2,3-e][1,2,4]triazolo[4,3-c]pyrimidines were prepared via oxidative cyclization of 4-(2-arylidenehydrazinyl)pyrido [3',2':4,5]thieno[3,2-d] pyrimidines. Dimroth rearrangement of such a series yielded pyrido[3',2':4,5]thieno[2,3-e][1,2,4]triazolo[1,5-c]pyrimidines. The reaction mechanism was proposed and the products were screened for their antimicrobial and anticancer activities. From the antimicrobial screening results, it can be seen that compounds 8c, 9f and 10c showed excellent activity against gram positive bacteria while compounds 10d and 8c showed the
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Dissertations / Theses on the topic "Amino-pyrimidines and Antimicrobial activity"

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Karpin, George W. "Synthesis and Antimicrobial Activity of Half-Sandwich Ir(III), Rh(III), and Co(III) Complexes." Diss., Virginia Tech, 2017. http://hdl.handle.net/10919/79414.

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This dissertation describes the synthesis and antimicrobial use of a series of half-sandwich Ir(III), Rh(III), Co(III) amino acid and ethylenediamine complexes. This investigation focuses on the formulation (ηn-arene)M(L)X, (L = ethylenediamine or α-amino carboxylate), (M= Ir, Rh, Ru, Co). Arene, Ligand and metal center variations were designed to tailor antimicrobial activity specific for each organism studied (Staphylococcus aureus or Mycobacteria). Each of the D/L-amino acids formed a diasteromeric complex with chiral centers on both the metal center and amino acid ligand. The unique chira
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Torres, Alba Fabiola Costa. "AÃÃo antibacteriana antifÃngica e antiparasitÃria de veneno de serpentes do gÃnero Bothrops e suas fraÃÃes fosfolipase A2 e L-AminoÃcido oxidase." Universidade Federal do CearÃ, 2009. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=3129.

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CoordenaÃÃo de AperfeiÃoamento de Pessoal de NÃvel Superior<br>Os venenos de serpentes contem substÃncias biologicamente ativas, primariamente consistindo de proteÃnas (90-95%). Algumas delas apresentam atividade enzimÃtica como as fosfolipases A2 e L-aminoÃcido oxidase. O presente estudo verificou a aÃÃo dos venenos de Bothrops leucurus (BleuVT) e Bothrops marajoensis (BmarVT), e suas fraÃÃes PLA2 (BleuPLA2 e BmarPLA2) e LAAO (BleuLAAO e BmarLAAO) sobre cepas de bactÃria, C. albicans, Leishmania sp e T. cruzi, bem com sua toxicidade sobre macrÃfagos murinos. A susceptibilidade das cepas bacte
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Osei-Boadi, Kate. ""An aliphatic essential amino acid influences the expression of host defense peptides in colonic epithelial cells: in vitro findings and potential clinical implications in Crohn's disease"." Diss., Kansas State University, 2014. http://hdl.handle.net/2097/17629.

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Doctor of Philosophy<br>Department of Human Nutrition<br>Tonatiuh Melgarejo<br>Background and Objective: Crohn’s disease (CD) patients express low levels of host defense peptides (HDPs) especially β-defensins, which may compromise intestinal barrier function. Antibiotic treatment for bacterial infections in CD is limited and rarely curative, making it necessary to find alternative therapeutic approaches. We therefore investigated to what extent an essential amino acid; L-isoleucine (L-ILE) might induce the expression of human β-defensins (HBDs) in colonic epithelial cells as an alternative ap
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Joaquim, Angélica Rocha. "Síntese de derivados de 8-hidroxiquinolina e avaliação da atividade antimicrobiana." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2018. http://hdl.handle.net/10183/181465.

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A prospecção e síntese de novos derivados de 8-hidroxiquinolina está em ascensão devido às suas diversas atividades biológicas. Neste trabalho é relatada a síntese e avaliação da atividade antimicrobiana de novos derivados contendo uma sulfonamida substituída na posição 5 da 8-hidroxiquinolina ou um grupamento aminossubstituído na posição 7 da 5-cloro-8-hidroxiquinolina ou 5-cloro-8-metoxiquinolina. Os derivados 5-sulfonamidas foram preparados por clorossulfonação seguida da reação com a amina apropriada. Os derivados 7-aminossubstituído foram sintetizados através da metilação da hidroxila da
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Wang, Siou Ying, and 王琇塋. "Correlations Between Bulky Non-natural Amino Acid Substitution and Anti-endotoxin Activity in the Antimicrobial Peptide P-113." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/q4sw7y.

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"Specific Amino Acid Substitutions Improve the Activity and Specificity of an Antimicrobial Peptide & Serodiagnosis by Immunosignature: a Multiplexing Tool for Monitoring the Humoral Immune Response to Dengue." Master's thesis, 2013. http://hdl.handle.net/2286/R.I.18114.

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abstract: Random peptide microarrays are a powerful tool for both the treatment and diagnostics of infectious diseases. On the treatment side, selected random peptides on the microarray have either binding or lytic potency against certain pathogens cells, thus they can be synthesized into new antimicrobial agents, denoted as synbodies (synthetic antibodies). On the diagnostic side, serum containing specific infection-related antibodies create unique and distinct "pathogen-immunosignatures" on the random peptide microarray distinct from the healthy control serum, and this different mode of bind
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Riahi, Abdol Majid [Verfasser]. "Synthesis of functionalized arenes based on (3+3) cyclizations of 1,3-bis(silyloxy)-1,3-butadienes with sulfone-, ester-, amino-, and nitro-substituted enones and antimicrobial activity of pyridyl enones / vorgelegt von Abdol Majid Riahi." 2009. http://d-nb.info/998565709/34.

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Book chapters on the topic "Amino-pyrimidines and Antimicrobial activity"

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Hammond, Katharine, Bart W. Hoogenboom, and Maxim G. Ryadnov. "Membrane disrupting peptides: mechanistic elucidation of antimicrobial activity." In Amino Acids, Peptides and Proteins. Royal Society of Chemistry, 2020. http://dx.doi.org/10.1039/9781788017008-00115.

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Tossi, Alessandro, Marco Scocchi, Sotir Zahariev, and Renato Gennaro. "Use of Unnatural Amino Acids to Probe Structure–Activity Relationships and Mode-of-Action of Antimicrobial Peptides." In Methods in Molecular Biology. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-331-8_10.

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Filipowska, Anna, Wojciech Filipowski, Ewaryst Tkacz, and Monika Wujec. "Statistical Analysis of the Impact of Molecular Descriptors on Antimicrobial Activity of Thiourea Derivatives Incorporating 3-amino-1,2,4-triazole Scaffold." In Innovations in Biomedical Engineering. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-70063-2_19.

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Ouertani, Awatef, Amor Mosbah, and Ameur Cherif. "Anti-Microbial Peptides: The Importance of Structure-Function Analysis in the Design of New AMPs." In Antimicrobial Peptides [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.99801.

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In recent years the rapid emergence of drug resistant microorganisms has become a major health problem worldwide. The number of multidrug resistant (MDR) bacteria is in a rapid increase. Therefore, there is an urgent need to develop new antimicrobial agent that is active against MDR. Among the possible candidates, antimicrobial peptides (AMPs) represent a promising alternative. Many AMPs candidates were in clinical development and the Nisin was approved in many food products. Exact mechanism of AMPs action has not been fully elucidated. More comprehensive of the mechanism of action provide a p
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Pushpabai Rajesh, Rajaian, and Grace Vanathi M. "Antimicrobial Peptides Derived from Ascidians and Associated Cyanobacteria." In Insights on Antimicrobial Peptides. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.99183.

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Ascidians belonging to Phylum Chordata are the most largest and diverse of the Sub-phylum Tunicata (Urochordata). Marine ascidians are one of the richest sources of bioactive peptides. These bioactive peptides from marine ascidians are confined to various types of structures such as cyclic peptides, acyclic peptides (depsipeptides), linear helical peptides with abundance of one amino acid (proline, trytophane, histidine), peptides forming hairpin like beta sheets or α-helical/β-sheet mixed structures stabilized by intra molecular disulfide bonding. Cyanobactins are fabricated through the prote
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Bie, Xiaomei. "Fengycin Production and Its Applications in Plant Growth and Postharvest Quality." In Bio-Based Antimicrobial Agents to Improve Agricultural and Food Safety. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815256239124010006.

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Fengycin is a cyclic lipopeptide produced mainly by the Bacillus genus, which is structurally composed of a β-hydroxy fatty acid and 10 amino acids. The biosynthesis of fengycin is catalyzed by large non-ribosomal peptide synthetases. Fengycin is an amphiphilic molecule with strong surface activity and displays strong antimicrobial activity. In this chapter, the molecular structure and biological properties of fengycin, and the function and catalyzing mechanism of fengycin multienzyme were summarized. Multiple antimicrobial mechanisms of fengycin and the strategies for increasing the productio
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Alhaj, Omar Amin. "Exploring Potential Therapeutic Properties of Camel Milk." In Handbook of Research on Health and Environmental Benefits of Camel Products. IGI Global, 2020. http://dx.doi.org/10.4018/978-1-7998-1604-1.ch007.

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This chapter highlights the potential health benefits of camel milk including antioxidant, anti-cancer activity, antihypertensive properties, antidiabetic activity, antimicrobial activity, hypoallergenicity activity, and anti-Crohn's disease. In addition to the most recent identified functional properties of camel milk. The bioactivity of conjugated linoleic acid (CLA), D and L amino acid, as well as oligosaccharide in camel milk will be also discussed. The proposed mechanisms behind these properties and potential health benefits are explained. This chapter also describes composition and nutri
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Jafeena, A. A., M. R. Ezhilarasi, and M. Suganthi. "SYNTHESIS, SPECTRAL CHARACTERIZATION, INSILCOMOLECULAR DOCKING STUDIES AND IN-VITRO ANTIMICROBIAL STUDIES OF 5-(4-SUBSTITUTED PHENYL)-3-(THIOPHEN-2-YL)-4, 5-DIHYDROPYRAZOLE-1-CARBOTHOAMIDE DERIVATIVES." In Futuristic Trends in Chemical Material Sciences & Nano Technology Volume 3 Book 11. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3becs11p2ch5.

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Using the melting point, Infra-red, 1-D1H and 13C NMR spectroscopic data, a new series of pyrimidines were harmonized and characterized. In vitro biological activities of all the harmonized compounds are tested. Also the same compound is tested by zone of inhibition against set of bacterial and fungal strains; by this the compound 2a tested against S.Aureus,S.Pyogenes, E.Coli, 4b against P.Aeruginosa, and this shows an excellent antibacterial activity. Similarly the compound 2c can show inhibition against C.albicans. And also all the compounds were undergone in-silico molecular docking predict
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Kreil, Gunther. "Skin secretions of Xenopus laevis." In The Biology of Xenopus. Oxford University PressOxford, 1996. http://dx.doi.org/10.1093/oso/9780198549741.003.0014.

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Abstract A variety of peptides, enzymes and other proteins have been isolated from skin secretions of Amphibia. Among the peptides at least three different groups can be discerned: (1) those with structural and functional homology to mammalian hormones and neurotransmitters; (2) antimicrobial peptides of different types, one being characterized by the propensity to form amphipathic helices; and (3) opioid peptides containing a D-amino acid essential for biological activity, for which no mammalian counterparts have so far been found. Of the first group, thyrotropin releasing hormone, caerulein
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Katas, Haliza. "Chitosan-Based Nanoparticles in Tissue Regeneration." In Functional Bio-based Materials for Regenerative Medicine: From Bench to Bedside (Part 1). BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815123104123010006.

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Chitosan is a unique polymer owing to its cationic property that allows interactions with various biological entities and is subsequently produced into novel functional products for biomedical applications, including tissue regeneration. Its cationic nature is conferred by amino groups present in its structure that are also responsible for various properties, including antibacterial activity. Chitosan is a biomaterial that has been extensively used in tissue engineering due to its ability to facilitate three-dimensional (3D) cell growth and proliferation as well as organize the deposition of c
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Conference papers on the topic "Amino-pyrimidines and Antimicrobial activity"

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Basha, N. Hussain, T. Rekha, G. Sravya, N. Bakthavatchala Reddy, Grigory V. Zyryanov, and V. Padmavathi. "Azolyl pyrimidines-synthesis and antimicrobial activity." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0070395.

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Mangalagiu, Violeta, Dumitrela Diaconu, and Ionel Mangalagiu. "Quinoline - sulfonamide - complexes with antimicrobial activity." In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab26.

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Quinoline-sulfonamide-complexes with variously metals, especially M2+, are a relatively new class of compounds with potential practical interest as fluorescent materials (having fotoluminiscent properties) and also as drugs (having a large variety of biological activities such as antibacterial, antifungal, antiprotozoals, etc.). The emphasis of this work was to obtain hybrid quinoline – sulfonamide - complexes with antimicrobial activity. The synthesis of the hybrid derivatives is direct and efficient, in two steps: acylation of variously amino-quinoline followed by metal complexation with dif
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Avdović, Edina, Žiko B. Milanović, Milanka Radulović, and Dušan S. Dimić. "ANTIMICROBIAL ACTIVITY OF 3- (1- (3- HYDROXYPHENYL) AMINO) ETHYLIDENE) CHROMAN-2,4-DIONE AND ITS CORRESPONDING PALLADIUM(II) COMPLEX." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.387a.

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In this manuscript, the in vitro antimicrobial activity of the previously synthesized coumarin derivative 3- (1- (3-hydroxyphenyl) amino) ethylidene) chroman-2,4-dione (L) and its corresponding palladium (II) complex (C) were examined. Their antimicrobial activity was screened against four strains of bacteria Bacillus cereus (ATCC 11778) G+; Staphylococcus aureus (ATCC 13709) G+; Klebsiella pneumoniae (ATCC 27736) G-; and Escherichia coli (ATCC 2592) G-) and three strains of fungi (Aspergillus flavus (ATCC15517); Candida albicans (ATCC 10231); Fusarium oxysporum (ATCC 695) using disc diffusion
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Biondi, Barbara, Fernando Formaggio, Cristina Peggion, et al. "Synthesis and biological activity of ultra-short antimicrobial peptides bearing a novel non-coded amino acid." In 37th European Peptide Symposium. The European Peptide Society, 2024. http://dx.doi.org/10.17952/37eps.2024.p1036.

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Bhanjana, Gaurav, Neeraj Kumar, Rajesh Thakur та ін. "Antimicrobial Activity of Metal & Metal Oxide Nanoparticles Interfaced With Ligand Complexes Of 8-Hydroxyquinoline And α-Amino Acids". У INTERNATIONAL CONFERENCE ON ADVANCES IN CONDENSED AND NANO MATERIALS (ICACNM-2011). AIP, 2011. http://dx.doi.org/10.1063/1.3653665.

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Ganapathy, Ramanan, and Ahmet Aykaç. "Depolymerisation of High Molecular Weight Chitosan and Its Impact on Purity and Deacetylation." In 6th International Students Science Congress. Izmir International Guest Student Association, 2022. http://dx.doi.org/10.52460/issc.2022.048.

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Chitosan (poly[β-(1-4)-2-amino-2-deoxy-d-glucopyranose]) is a non-toxic and biocompatible cationic polysaccharide produced by partial deacetylation of chitin isolated from naturally occurring crustacean shells. Its low solubility limits its application, improving the solubility by reducing the molecular weight, increases its wide application in food, agriculture, pharmaceutical and other technical applications. Low molecular weight chitosan, acts as a potent biotic elicitor, induce plant defense responses, activating different pathways that increase the crop resistance to diseases. Antimicrobi
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Reports on the topic "Amino-pyrimidines and Antimicrobial activity"

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Verkleij, T. J., and P. Voudouris. Determination of the antimicrobial activity of the amino acid L-isoleucine. Wageningen Food & Biobased Research, 2022. https://doi.org/10.18174/581250.

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Verkleij, T. J., P. Voudouris, Jeroen Hugenholtz, and Marieke Bruins. Determination of the antimicrobial activity of amino acid zootechnical mix : Three different batches examined. Wageningen Food & Biobased Research, 2022. http://dx.doi.org/10.18174/566497.

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Alexandar, Irina, Diana Zasheva, and Nikolay Kaloyanov. Antimicrobial Activity of New Molecular Complexes of 1,10‑Phenanthroline and 5‑Amino‑1,10‑Phenanthroline on Escherichia coli and Saccharomyces cerevisiae Strains. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, 2019. http://dx.doi.org/10.7546/crabs.2019.01.10.

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