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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Infectious Disorders - Drug Targets</journal-id><journal-title-group><journal-title xml:lang="en">Infectious Disorders - Drug Targets</journal-title><trans-title-group xml:lang="ru"><trans-title>Infectious Disorders - Drug Targets</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1871-5265</issn><issn publication-format="electronic">2212-3989</issn><publisher><publisher-name xml:lang="en">Bentham Science</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">645762</article-id><article-id pub-id-type="doi">10.2174/0118715265274067240223040333</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Medicine</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Imidazo[1,2-A]Pyridine: Potent Biological Activity, SAR and Docking Investigations (2017-2022)</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Narayan</surname><given-names>Aditya</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Patel</surname><given-names>Shivkant</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Baile</surname><given-names>Sunil</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Jain</surname><given-names>Surabhi</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name><surname>Sharma</surname><given-names>Smriti</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff4"/></contrib></contrib-group><aff id="aff1"><institution>Centre for Pharmaceutical Engineering Science, School of Pharmacy and Medical Sciences, University of Bradford</institution></aff><aff id="aff2"><institution>Department of Pharmacy, Sumandeep Vidyapeeth Deemed to be University</institution></aff><aff id="aff3"><institution>B. Pharmacy College Rampura-kakanpur, Gujarat Technological University</institution></aff><aff id="aff4"><institution>Amity Institute of Pharmacy,, Amity University</institution></aff><pub-date date-type="pub" iso-8601-date="2024-08-01" publication-format="electronic"><day>01</day><month>08</month><year>2024</year></pub-date><volume>24</volume><issue>8</issue><issue-title xml:lang="ru"/><history><date date-type="received" iso-8601-date="2025-01-11"><day>11</day><month>01</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Bentham Science Publishers</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Bentham Science Publishers</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://journals.eco-vector.com/1871-5265/article/view/645762">https://journals.eco-vector.com/1871-5265/article/view/645762</self-uri><abstract xml:lang="en"><p id="idm46466589573568">Background:Regarding scientific research, Imidazo[1,2-a] pyridine derivatives are constantly being developed due to the scaffolds intriguing chemical structure and varied bio-logical activity. They are distinctive organic nitrogen-bridged heterocyclic compounds that have several uses in medicines, organometallics and natural products. It has become a vital tool for medicinal chemists.</p><p id="idm46466589577568">Methods:In order to gather scientific information on Imidazo[1,2-a] pyridines derivative, Google, PubMed, Scopus, Google Scholar, and other databases were searched. In the current study, the medicinal value and therapeutic effect of Imidazo[1,2-a] pyridines were investigated using above mentioned databases. The current study analyzed the detailed pharmacological ac-tivities of Imidazo[1,2-a] pyridine analogs through literature from diverse scientific research works.</p><p id="idm46466589581536">Results:Due to its wide range of biological activities, including antiulcer, anticonvulsant, anti-protozoal, anthelmintic, antiepileptic, antifungal, antibacterial, analgesic, antiviral, anticancer, anti-inflammatory, antituberculosis, and antitumor properties, imidazopyridine is one of the most significant structural skeletons in the field of natural and pharmaceutical products. An imidazopyridine scaffold serves as the basis for a number of therapeutically utilized medica-tions, including zolpidem, alpidem, olprinone, zolimidine, and necopidem.</p><p id="idm46466589586592">Conclusion:This comprehensive study covers the period of the last five years, and it sheds light on the developments and emerging pharmacological actions of Imidazo[1,2-a] pyridines. Additionally, the structure-activity relationship and molecular docking studies are carefully documented throughout the paper, providing medicinal chemists with a clear picture for devel-oping new drugs.</p></abstract><kwd-group xml:lang="en"><kwd>Nitrogen-based heterocycle</kwd><kwd>imidazo[1,2-a] pyridine</kwd><kwd>biological sctivities</kwd><kwd>synthesis</kwd><kwd>SAR analysis</kwd><kwd>antimicrobial</kwd><kwd>anticancer</kwd><kwd>anticonvulsant</kwd><kwd>antiviral.</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Bagdi AK, Mitra S, Ghosh M, Hajra A. Iodine-catalyzed regioselective thiolation of imidazo1,2-apyridines using sulfonyl hydrazides as a thiol surrogate. Org Biomol Chem 2015; 13(11): 3314-20. doi: 10.1039/C5OB00033E PMID: 25644749</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Kang S, Kim YM, Kim RY, et al. 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