<HashMap><database>biostudies-literature</database><scores/><additional><submitter>El Mahdaoui A</submitter><funding>Fonds de la Recherche Scientifique—FNRS</funding><funding>COST action</funding><funding>FNRS</funding><funding>European Cooperation in Science and Technology</funding><funding>CNRST</funding><funding>Centre National de la Recherche Scientifique et Technologique</funding><pagination>1186</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10935173</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(5)</volume><pubmed_abstract>In this study, we synthesized two coordination complexes based on pyrazole-based ligands, namely 1,5-dimethyl-&lt;i>N&lt;/i>-phenyl-1H-pyrazole-3-carboxamide (&lt;b>L&lt;sub>1&lt;/sub>&lt;/b>) and 1,5-dimethyl-&lt;i>N&lt;/i>-propyl-1H-pyrazole-3-carboxamide (&lt;b>L&lt;sub>2&lt;/sub>&lt;/b>), with the aim to investigate bio-inorganic properties. Their crystal structures revealed a mononuclear complex [Ni(&lt;b>L&lt;sub>1&lt;/sub>&lt;/b>)&lt;sub>2&lt;/sub>](ClO&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub> (&lt;b>C&lt;sub>1&lt;/sub>&lt;/b>) and a dinuclear complex [Cd&lt;sub>2&lt;/sub>(&lt;b>L&lt;sub>2&lt;/sub>&lt;/b>)&lt;sub>2&lt;/sub>]Cl&lt;sub>4&lt;/sub> (&lt;b>C&lt;sub>2&lt;/sub>&lt;/b>). Very competitive antifungal and anti-Fusarium activities were found compared to the reference standard cycloheximide. Additionally, &lt;b>L&lt;sub>1&lt;/sub>&lt;/b> and &lt;b>L&lt;sub>2&lt;/sub>&lt;/b> present very weak genotoxicity in contrast to the observed increase in genotoxicity for the coordination complexes &lt;b>C&lt;sub>1&lt;/sub>&lt;/b> and &lt;b>C&lt;sub>2&lt;/sub>&lt;/b>.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Synthesis, Crystal Structures, Genotoxicity, and Antifungal and Antibacterial Studies of Ni(II) and Cd(II) Pyrazole Amide Coordination Complexes.</pubmed_title><pmcid>PMC10935173</pmcid><funding_grant_id>CDR J.0064.23</funding_grant_id><funding_grant_id>PPR2-MESRSFC-CNRSTP10</funding_grant_id><funding_grant_id>EQP U.N027.24</funding_grant_id><funding_grant_id>CA21149</funding_grant_id><funding_grant_id>PDR T.0095.21, CDR J.0064.23, J.0168.22, EQP U.N027.24</funding_grant_id><funding_grant_id>J.0168.22</funding_grant_id><funding_grant_id>PDR T.0095.21</funding_grant_id><pubmed_authors>Garcia Y</pubmed_authors><pubmed_authors>Ouahhoud S</pubmed_authors><pubmed_authors>Radi S</pubmed_authors><pubmed_authors>Draoui Y</pubmed_authors><pubmed_authors>El Massaoudi M</pubmed_authors><pubmed_authors>Saalaoui E</pubmed_authors><pubmed_authors>Benabbes R</pubmed_authors><pubmed_authors>El Mahdaoui A</pubmed_authors><pubmed_authors>Bentouhami NE</pubmed_authors><pubmed_authors>Asehraou A</pubmed_authors><pubmed_authors>Robeyns K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis, Crystal Structures, Genotoxicity, and Antifungal and Antibacterial Studies of Ni(II) and Cd(II) Pyrazole Amide Coordination Complexes.</name><description>In this study, we synthesized two coordination complexes based on pyrazole-based ligands, namely 1,5-dimethyl-&lt;i>N&lt;/i>-phenyl-1H-pyrazole-3-carboxamide (&lt;b>L&lt;sub>1&lt;/sub>&lt;/b>) and 1,5-dimethyl-&lt;i>N&lt;/i>-propyl-1H-pyrazole-3-carboxamide (&lt;b>L&lt;sub>2&lt;/sub>&lt;/b>), with the aim to investigate bio-inorganic properties. Their crystal structures revealed a mononuclear complex [Ni(&lt;b>L&lt;sub>1&lt;/sub>&lt;/b>)&lt;sub>2&lt;/sub>](ClO&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub> (&lt;b>C&lt;sub>1&lt;/sub>&lt;/b>) and a dinuclear complex [Cd&lt;sub>2&lt;/sub>(&lt;b>L&lt;sub>2&lt;/sub>&lt;/b>)&lt;sub>2&lt;/sub>]Cl&lt;sub>4&lt;/sub> (&lt;b>C&lt;sub>2&lt;/sub>&lt;/b>). Very competitive antifungal and anti-Fusarium activities were found compared to the reference standard cycloheximide. Additionally, &lt;b>L&lt;sub>1&lt;/sub>&lt;/b> and &lt;b>L&lt;sub>2&lt;/sub>&lt;/b> present very weak genotoxicity in contrast to the observed increase in genotoxicity for the coordination complexes &lt;b>C&lt;sub>1&lt;/sub>&lt;/b> and &lt;b>C&lt;sub>2&lt;/sub>&lt;/b>.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-26T03:25:33.333Z</modification><creation>2025-04-06T14:35:30.958Z</creation></dates><accession>S-EPMC10935173</accession><cross_references><pubmed>38474698</pubmed><doi>10.3390/molecules29051186</doi></cross_references></HashMap>