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Mendeleev Communications, 2021, Volume 31, Issue 2, Pages 204–206
DOI: https://doi.org/10.1016/j.mencom.2021.03.019
(Mi mendc879)
 

This article is cited in 17 scientific papers (total in 17 papers)

Communications

Antibacterial activity of new silatrane pyrrole-2-carboxamide hybrids

S. N. Adamovich, E. Kh. Sadykov, I. A. Ushakov, E. N. Oborina, L. A. Belovezhets

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
Abstract: Silatrane-1H-pyrrole-2-carboxamide hybrids conjugated via propane-1,3-diyl linker have been synthesized by the reaction of 1-(3-aminopropyl)silatrane with 2-(trichloroacetyl)pyrroles. Their in silico screening would predict their antitumor activity. Their in vitro screening for antimicrobial activity revealed the representative with R1=R2=R3=H to be the most potent against Gram-positive microorganisms such as E. durans, B. subtilis and E. coli.
Keywords: silatranes, pyrrolecarboxamides, hybrids, antitumor activity, antimicrobial action.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (979.2 Kb)


Citation: S. N. Adamovich, E. Kh. Sadykov, I. A. Ushakov, E. N. Oborina, L. A. Belovezhets, “Antibacterial activity of new silatrane pyrrole-2-carboxamide hybrids”, Mendeleev Commun., 31:2 (2021), 204–206
Linking options:
  • https://www.mathnet.ru/eng/mendc879
  • https://www.mathnet.ru/eng/mendc/v31/i2/p204
  • This publication is cited in the following 17 articles:
    1. Gurjaspreet Singh, Pawan, Manickam Selvaraj, Harshbir Kaur, Brij Mohan, Amarjit Kaur, Sanchita, “Anthracene‐Based Schiff Base Allied Triazolyl Silatranes: A Comparison of Stability and Biological Activity With Open Analog Silane”, Applied Organom Chemis, 39:2 (2025)  crossref
    2. Bhaskar Sahu, Rakesh Sahu, Bina Gidwani, Achal Mishra, “Pyrrole: An Essential Framework in the Development of Therapeutic Agents and Insightful Analysis of Structure‐Active Relationships”, ChemistrySelect, 9:31 (2024)  crossref
    3. Jenny-Lee Panayides, Darren Lyall Riley, Felix Hasenmaile, Willem A. L. van Otterlo, “The role of silicon in drug discovery: a review”, RSC Med. Chem., 15:10 (2024), 3286  crossref
    4. Nadezhda V. Vchislo, Sergey N. Adamovich, Victoria G. Fedoseeva, Elizaveta N. Oborina, Igor B. Rozentsveig, Francis Verpoort, “Schiff Base of 3‐Aminopropylalkoxysilanes and 3‐Aminopropylsilatranes: Importance of Investigations and the Potential Applications”, Applied Organom Chemis, 38:12 (2024)  crossref
    5. Aura Rusu, Octavia-Laura Oancea, Corneliu Tanase, Livia Uncu, “Unlocking the Potential of Pyrrole: Recent Advances in New Pyrrole-Containing Compounds with Antibacterial Potential”, IJMS, 25:23 (2024), 12873  crossref
    6. Anh Thu Nguyen Tran, Zhiyuan Wu, Duy T. M. Chung, Phattananawee Nalaoh, Jonathan S. Lindsey, “Synthesis of model southern rim structures of photosynthetic tetrapyrroles and phyllobilins”, New J. Chem., 47:29 (2023), 13626  crossref
    7. Sergey N. Adamovich, Igor A. Ushakov, Elizaveta N. Oborina, Svetlana V. Lukyanova, Vladislav Y. Komarov, “New 3-Aminopropylsilatrane Derivatives: Synthesis, Structure, Properties, and Biological Activity”, IJMS, 24:12 (2023), 9965  crossref
    8. Ghasem Rezanejade Bardajee, Hossein Mahmoodian, Seyed Ata Boraghi, Fatemeh Aghazadeh, Zahir Rezanejad, “A facile and efficient synthesis of highly functionalized pyrroles via a four-component one-pot reaction in the presence of Ni(II) Schiff base/SBA-15 heterogeneous catalyst”, Res Chem Intermed, 49:5 (2023), 1959  crossref
    9. S. N. Adamovich, E. N. Oborina, M. D. Katerinich, “3-Aminopropyltrietoxysilane and –Silatrane in the Michael Aza-Reaction with Acrylates. Synthesis, Structure, and Properties of Adducts”, Russ J Gen Chem, 93:S1 (2023), S210  crossref
    10. Sergey N. Adamovich, Arailym M. Nalibayeva, Yerlan N. Abdikalykov, Igor A. Ushakov, Elizaveta N. Oborina, Igor B. Rozentsveig, “New Functional Alkoxysilanes and Silatranes: Synthesis, Structure, Properties, and Possible Applications”, IJMS, 24:18 (2023), 13818  crossref
    11. Gurjaspreet Singh, Sushma, Priyanka, Anita Devi, Tamana, Harshbir Kaur, Mithun, Jandeep Singh, Gurleen Singh, “A dual response UV-vis and fluorescence receptor based on acetylenic-indole conjoined silatrane for selective recognition of Co2+ and Cu2+ ions and in silico antidiabetic activity”, New J. Chem., 47:48 (2023), 22441  crossref
    12. I. S. Ignatyev, Yu. A. Kondratenko, D. V. Lezov, V. L. Ugolkov, T. A. Kochina, “Hexacoordinate germanium compounds with BIS-TRIS and amino acid ligands”, Mendeleev Commun., 33:5 (2023), 601–604  mathnet  crossref
    13. Yulia A. Kondratenko, Igor S. Ignatyev, Denis V. Lezov, Maxim Y. Arsent'ev, Andrey A. Zolotarev, Valerii L. Ugolkov, Dmitrii Antuganov, Tatyana A. Kochina, “Synthesis and characterization of hypercoordinated germanium complexes with hydroxyalkylethylenediamines”, Journal of Organometallic Chemistry, 958 (2022), 122188  crossref
    14. Sergey N. Adamovich, Elizaveta N. Oborina, Arailym M. Nalibayeva, Igor B. Rozentsveig, “3-Aminopropylsilatrane and Its Derivatives: A Variety of Applications”, Molecules, 27:11 (2022), 3549  crossref
    15. S. V. Lukyanova, S. N. Adamovich, Zh. A. Konovalova, E. N. Oborina, N. G. Gefan, A. S. Ostyak, V. I. Kuznetsov, N. A. Voichenko, “Silatrane-Sulfonamide Hybrids as Promising Antibacterial Agents”, Bull Exp Biol Med, 174:1 (2022), 66  crossref
    16. Mirela-Fernanda Zaltariov, Mihaela Turtoi, Dragos Peptanariu, Ana-Maria Macsim, Lilia Clima, Corneliu Cojocaru, Nicoleta Vornicu, Bianca-Iulia Ciubotaru, Alexandra Bargan, Manuela Calin, Maria Cazacu, “Chemical Attachment of 5-Nitrosalicylaldimine Motif to Silatrane Resulting in an Organic–Inorganic Structure with High Medicinal Significance”, Pharmaceutics, 14:12 (2022), 2838  crossref
    17. A. Mukherjee, D. S. Kopchuk, S. Santra, A. Majee, G. V. Zyryanov, O. N. Chupakhin, “Iron(iii) chloride-catalyzed mechanochemical cascade synthesis of highly-substituted pyrrolyl indoles”, Mendeleev Commun., 32:5 (2022), 624–626  mathnet  crossref
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