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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">Anti-Inflammatory &amp; Anti-Allergy Agents in Medicinal Chemistry</journal-id><journal-title-group><journal-title xml:lang="en">Anti-Inflammatory &amp; Anti-Allergy Agents in Medicinal Chemistry</journal-title><trans-title-group xml:lang="ru"><trans-title>Anti-Inflammatory &amp; Anti-Allergy Agents in Medicinal Chemistry</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1871-5230</issn><issn publication-format="electronic">1875-614X</issn><publisher><publisher-name xml:lang="en">Bentham Science</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">644650</article-id><article-id pub-id-type="doi">10.2174/0118715230282982240202052127</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">Analgesic and Anti-inflammatory Potential of the New Tetrahydropyran Derivative (2s,6s)-6-ethyl-tetrahydro-2h-pyran-2-yl) Methanol</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Castro</surname><given-names>Gustavo</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>de Souza</surname><given-names>Raquel</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>da Silva</surname><given-names>Alba</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Laureano-Melo</surname><given-names>Roberto</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name><surname>da Silva Côrtes</surname><given-names>Wellington</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name><surname>Capim</surname><given-names>Saulo</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff5"/></contrib><contrib contrib-type="author"><name><surname>de Almeida Vasconcellos</surname><given-names>Mário</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff6"/></contrib><contrib contrib-type="author"><name><surname>Marinho</surname><given-names>Bruno</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff id="aff1"><institution>Laboratório de Farmacologia da Inflamação e Nocicepção, Programa de Pós-Graduação em Medicina Veterinária, Instituto de Veterinária, Universidade Federal Rural do Rio de Janeiro</institution></aff><aff id="aff2"><institution>Laboratório de Cultura de Células, Instituto de Ciências Biológicas e da Saúde, Universidade Federal Rural do Rio de Janeiro</institution></aff><aff id="aff3"><institution>Laboratório de Fisiofarmacologia Comportamental, Centro Universitário de Barra Mansa</institution></aff><aff id="aff4"><institution>Laboratório de Psicofarmacologia e Comportamento, Programa de Pós-Graduação Multicêntrico em Ciências Fisiológicas, Instituto de Ciências Biológicas e da Saúde, Universidade Federal Rural do Rio de Janeiro</institution></aff><aff id="aff5"><institution>Instituto Federal de Educação, Ciência e Tecnologia Baiano, Federal Institute Baiano</institution></aff><aff id="aff6"><institution>Laboratório de Síntese Orgânica Medicinal da Paraíba (LASOM-PB), Departamento de Química, Universidade Federal da Paraíba</institution></aff><pub-date date-type="pub" iso-8601-date="2024-02-01" publication-format="electronic"><day>01</day><month>02</month><year>2024</year></pub-date><volume>23</volume><issue>2</issue><issue-title xml:lang="ru"/><fpage>105</fpage><lpage>117</lpage><history><date date-type="received" iso-8601-date="2025-01-07"><day>07</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/1871-5230/article/view/644650">https://journals.eco-vector.com/1871-5230/article/view/644650</self-uri><abstract xml:lang="en"><p id="idm46041443609680">Background:The development of analgesic and anti-inflammatory drugs plays a crucial role in modern medicine, aiming to alleviate pain and reduce inflammation in patients. Opioids and nonsteroidal anti-inflammatory drugs are groups of drugs conventionally used to treat pain and in-flammation, but a wide range of adverse effects and ineffectiveness in some pathological conditions leads us to search for new drugs with analgesic and anti-inflammatory properties.</p><p id="idm46041443613680">Objectives:In this regard, the authors intend to investigate the ((2s,6s)-6-ethyl-tetrahydro-2h-pyran-2-yl) methanol compound (LS20) on pain and acute inflammation.</p><p id="idm46041443617648">Methods:Male Swiss mice were evaluated using acetic acid-induced abdominal writhing, formalin, and tail-flick as models of nociceptive evaluation and edema paw, air pouch and cell culture as models of inflammatory evaluation besides the rotarod test for assessment of motor impairment.</p><p id="idm46041443622704">Results:The compound showed an effect on the acetic acid-induced abdominal writhing, formalin and tail-flick tests. Studying the mechanism of action, reversion of the antinociceptive effect of the compound was observed from previous intraperitoneal administration of selective and non-selective opioid antagonists on the tail flick test. In addition, the compound induced an antiedematogenic effect and reduced leukocyte migration and the production of pro-inflammatory cytokines in the air pouch model. LS20 was able to maintain cell viability, in addition to reducing cell production of TNF-α and IL-6.</p><p id="idm46041443632080">Conclusion:In summary, the LS20 compound presented an antinociceptive effect, demonstrating the participation of the opioid system and an anti-inflammatory effect related to the inhibition of pro-inflammatory cytokine production. The compound also demonstrated safety at the cellular level.</p></abstract><kwd-group xml:lang="en"><kwd>Tetrahydropyran derivative</kwd><kwd>mice</kwd><kwd>antinociceptive effect</kwd><kwd>opioid system</kwd><kwd>cytokines</kwd><kwd>inflammation.</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Raja, S.N.; Carr, D.B.; Cohen, M.; Finnerup, N.B.; Flor, H.; Gibson, S. The Revised IASP definition of pain: Concepts, challenges, and compromises. Pain, 2020, 161(9), 1976-1982. doi: 10.1097/j.pain.0000000000001939 PMID: 32694387</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Wang, L.H.; Ding, W.Q.; Sun, Y.G. Spinal ascending pathways for somatosensory information processing. Trends Neurosci., 2022, 45(8), 594-607. doi: 10.1016/j.tins.2022.05.005 PMID: 35701247</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Todd, A.J. Neuronal circuitry for pain processing in the dorsal horn. Nat. Rev. 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