Synthesis of New Chroman‐4‐one Based 1,2,3‐Triazole Analogues as Antioxidant and Anti‐Inflammatory Agents
A library of new chroman‐4‐one based 1,2,3‐triazole analogues were synthesized involving a series of condensation, cyclization, Suzuki coupling and copper catalysed click chemistry protocols. The newly synthesized compounds 8a–l were screened for their invitro antioxidant and anti‐inflammatory activ...
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Veröffentlicht in: | Chemistry & biodiversity 2024-07, Vol.21 (7), p.e202400587-n/a |
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description | A library of new chroman‐4‐one based 1,2,3‐triazole analogues were synthesized involving a series of condensation, cyclization, Suzuki coupling and copper catalysed click chemistry protocols. The newly synthesized compounds 8a–l were screened for their invitro antioxidant and anti‐inflammatory activities by employing Ascorbic acid and Diclofenac as reference drugs respectively. The compound without any substituent on benzyl ring (8a), compound with ‐Cl substituent in para position of benzyl ring (8i), and compound with ethoxy substituent in para position of benzyl ring (8k) exhibited potent antioxidant and anti‐inflammatory activities with higher percentage of inhibition. To understand their binding affinities, molecular docking study of these three compounds performed against NADPH oxidase with presented outstanding docking scores and promising binding interactions like H‐bond and hydrophobic. |
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The newly synthesized compounds 8a–l were screened for their invitro antioxidant and anti‐inflammatory activities by employing Ascorbic acid and Diclofenac as reference drugs respectively. The compound without any substituent on benzyl ring (8a), compound with ‐Cl substituent in para position of benzyl ring (8i), and compound with ethoxy substituent in para position of benzyl ring (8k) exhibited potent antioxidant and anti‐inflammatory activities with higher percentage of inhibition. 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To understand their binding affinities, molecular docking study of these three compounds performed against NADPH oxidase with presented outstanding docking scores and promising binding interactions like H‐bond and hydrophobic.</description><subject>anti-inflammatory</subject><subject>antioxidant</subject><subject>Antioxidants</subject><subject>Ascorbic acid</subject><subject>Binding</subject><subject>Chemical bonds</subject><subject>Chemical synthesis</subject><subject>Chroman-4-one</subject><subject>Diclofenac</subject><subject>Hydrophobicity</subject><subject>Inflammation</subject><subject>Molecular docking</subject><subject>NAD(P)H oxidase</subject><subject>NADPH oxidase</subject><subject>Triazoles</subject><issn>1612-1872</issn><issn>1612-1880</issn><issn>1612-1880</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkblOAzEQhi0E4gi0lMgSDUUSfOxhl0m4IiEoCLSrydobFu3aYG8IoeIReEaeBIdAkGgoLHvG3_yamR-hfUq6lBB2nI_Vc5cRFhESi3QNbdOEsg4Vgqyv3inbQjvePwQ-5MUm2uIipYKSaBs93cxNc6996bEt8JWe4cG9szWYj7f3KBxrNO6D1wrTNmvzkBm5El5tpXHPQGUnU-0x-BA0pX0pFZgGg1FfcYCHpqigrqGxbo57E20av4s2Cqi83vu-W-j27HQ0uOhcXp8PB73LTs7CJJ0oyhMFOqEJJEDzRCRjqXLGhCrCj2RjnoBOpRBSgpJFnOaxEjSKVShUike8hY6Wuo_OPoUum6wufa6rCoy2U59xEnPKRSzTgB7-QR_s1IXxFlTYk0gl4YHqLqncWe-dLrJHV9bg5hkl2cKMbGFGtjIjFBx8y07HtVYr_Gf7AZBLYFZWev6PXDbon9z9in8CRn2Y7Q</recordid><startdate>202407</startdate><enddate>202407</enddate><creator>Ambala, Shankaraiah</creator><creator>Thumma, Vishnu</creator><creator>Mallikanti, Veerabhadraiah</creator><creator>Bathini, Vineesha</creator><creator>K, Jyothi</creator><creator>Pochampally, Jalapathi</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5419-6868</orcidid><orcidid>https://orcid.org/0000-0001-6830-3671</orcidid></search><sort><creationdate>202407</creationdate><title>Synthesis of New Chroman‐4‐one Based 1,2,3‐Triazole Analogues as Antioxidant and Anti‐Inflammatory Agents</title><author>Ambala, Shankaraiah ; Thumma, Vishnu ; Mallikanti, Veerabhadraiah ; Bathini, Vineesha ; K, Jyothi ; Pochampally, Jalapathi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2587-44c6dae616a6a1c686b9dc228df4c692b36ae798899ad9f57c5d8145d44cdd343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>anti-inflammatory</topic><topic>antioxidant</topic><topic>Antioxidants</topic><topic>Ascorbic acid</topic><topic>Binding</topic><topic>Chemical bonds</topic><topic>Chemical synthesis</topic><topic>Chroman-4-one</topic><topic>Diclofenac</topic><topic>Hydrophobicity</topic><topic>Inflammation</topic><topic>Molecular docking</topic><topic>NAD(P)H oxidase</topic><topic>NADPH oxidase</topic><topic>Triazoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ambala, Shankaraiah</creatorcontrib><creatorcontrib>Thumma, Vishnu</creatorcontrib><creatorcontrib>Mallikanti, Veerabhadraiah</creatorcontrib><creatorcontrib>Bathini, Vineesha</creatorcontrib><creatorcontrib>K, Jyothi</creatorcontrib><creatorcontrib>Pochampally, Jalapathi</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry & biodiversity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ambala, Shankaraiah</au><au>Thumma, Vishnu</au><au>Mallikanti, Veerabhadraiah</au><au>Bathini, Vineesha</au><au>K, Jyothi</au><au>Pochampally, Jalapathi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of New Chroman‐4‐one Based 1,2,3‐Triazole Analogues as Antioxidant and Anti‐Inflammatory Agents</atitle><jtitle>Chemistry & biodiversity</jtitle><addtitle>Chem Biodivers</addtitle><date>2024-07</date><risdate>2024</risdate><volume>21</volume><issue>7</issue><spage>e202400587</spage><epage>n/a</epage><pages>e202400587-n/a</pages><issn>1612-1872</issn><issn>1612-1880</issn><eissn>1612-1880</eissn><abstract>A library of new chroman‐4‐one based 1,2,3‐triazole analogues were synthesized involving a series of condensation, cyclization, Suzuki coupling and copper catalysed click chemistry protocols. 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subjects | anti-inflammatory antioxidant Antioxidants Ascorbic acid Binding Chemical bonds Chemical synthesis Chroman-4-one Diclofenac Hydrophobicity Inflammation Molecular docking NAD(P)H oxidase NADPH oxidase Triazoles |
title | Synthesis of New Chroman‐4‐one Based 1,2,3‐Triazole Analogues as Antioxidant and Anti‐Inflammatory Agents |
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