<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li X</submitter><funding>National Natural Science Foundation of China (NSFC)</funding><pagination>12521</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10420152</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(15)</volume><pubmed_abstract>To better understand the potential toxicity risks of isoflucypram in humans, The interaction between isoflucypram and HSA (human serum albumin) was studied through molecular docking, molecular dynamics simulations, ultraviolet-visible absorption, fluorescence, synchronous fluorescence, three-dimensional fluorescence, Fourier transform infrared spectroscopies, and circular dichroism spectroscopies. The interaction details were studied using the molecular docking method and molecular dynamics simulation method. The results revealed that the effect of isoflucypram on human serum albumin was mixed (static and dynamic) quenching. Additionally, we were able to obtain important information on the number of binding sites, binding constants, and binding distance. The interaction between isoflucypra</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Probing the Interaction between Isoflucypram Fungicides and Human Serum Albumin: Multiple Spectroscopic and Molecular Modeling Investigations.</pubmed_title><pmcid>PMC10420152</pmcid><funding_grant_id>32072468</funding_grant_id><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Yang D</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Yuan H</pubmed_authors><pubmed_authors>Yan X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Probing the Interaction between Isoflucypram Fungicides and Human Serum Albumin: Multiple Spectroscopic and Molecular Modeling Investigations.</name><description>To better understand the potential toxicity risks of isoflucypram in humans, The interaction between isoflucypram and HSA (human serum albumin) was studied through molecular docking, molecular dynamics simulations, ultraviolet-visible absorption, fluorescence, synchronous fluorescence, three-dimensional fluorescence, Fourier transform infrared spectroscopies, and circular dichroism spectroscopies. The interaction details were studied using the molecular docking method and molecular dynamics simulation method. The results revealed that the effect of isoflucypram on human serum albumin was mixed (static and dynamic) quenching. Additionally, we were able to obtain important information on the number of binding sites, binding constants, and binding distance. The interaction between isoflucypra</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Aug</publication><modification>2025-04-27T00:09:03.225Z</modification><creation>2025-04-06T17:49:51.602Z</creation></dates><accession>S-EPMC10420152</accession><cross_references><pubmed>37569896</pubmed><doi>10.3390/ijms241512521</doi></cross_references></HashMap>