<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(7)</volume><submitter>Uma Priya K</submitter><pubmed_abstract>A series of new sulphonamide and carbamate derivatives of Nebivolol drug intermediate (5) were designed and synthesized by reacting various biopotent sulphonylchlorides and chloroformates. The synthesized compounds are structurally characterized by spectral (IR, &lt;sup>1&lt;/sup>H &amp; &lt;sup>13&lt;/sup>C NMR and mass) and screened for their &lt;i>in vitro&lt;/i> antimicrobial activity against four bacterial and three fungal strains, &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i> antiinflammatory activity against LPS-induced inflammation in RAW 264.7, &lt;i>in vitro&lt;/i> COX-1 and COX-2 inhibition potentiality, antagonistic profiles of carrageenan induced paw edema and cotton pellet induced granuloma in rat. Further, the compounds were screened for their antimicrobial and antiinflammatory activity against DNA gyrase A, COX-</pubmed_abstract><journal>RSC advances</journal><pagination>3897-3916</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8694313</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Design, synthesis, characterization and &lt;i>in vitro, in vivo&lt;/i> and &lt;i>in silico&lt;/i> antimicrobial and antiinflammatory activities of a new series of sulphonamide and carbamate derivatives of a nebivolol intermediate.</pubmed_title><pmcid>PMC8694313</pmcid><pubmed_authors>Uma Priya K</pubmed_authors><pubmed_authors>Raju CN</pubmed_authors><pubmed_authors>Sreedhar NY</pubmed_authors><pubmed_authors>Venkataramaiah C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Design, synthesis, characterization and &lt;i>in vitro, in vivo&lt;/i> and &lt;i>in silico&lt;/i> antimicrobial and antiinflammatory activities of a new series of sulphonamide and carbamate derivatives of a nebivolol intermediate.</name><description>A series of new sulphonamide and carbamate derivatives of Nebivolol drug intermediate (5) were designed and synthesized by reacting various biopotent sulphonylchlorides and chloroformates. The synthesized compounds are structurally characterized by spectral (IR, &lt;sup>1&lt;/sup>H &amp; &lt;sup>13&lt;/sup>C NMR and mass) and screened for their &lt;i>in vitro&lt;/i> antimicrobial activity against four bacterial and three fungal strains, &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i> antiinflammatory activity against LPS-induced inflammation in RAW 264.7, &lt;i>in vitro&lt;/i> COX-1 and COX-2 inhibition potentiality, antagonistic profiles of carrageenan induced paw edema and cotton pellet induced granuloma in rat. Further, the compounds were screened for their antimicrobial and antiinflammatory activity against DNA gyrase A, COX-</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jan</publication><modification>2026-05-31T18:48:20.555Z</modification><creation>2024-11-21T09:52:26.122Z</creation></dates><accession>S-EPMC8694313</accession><cross_references><pubmed>35424332</pubmed><doi>10.1039/d0ra08905b</doi></cross_references></HashMap>