{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["24(17)"],"submitter":["Lodyga-Chruscinska E"],"pubmed_abstract":["Structure-related biological activities of flavanones are still considered largely unexplored. Since they exhibit various medicinal activities, it is intriguing to enter deeper into their chemical structures, electronic transitions or interactions with some biomolecules in order to find properties that allow us to better understand their effects. Little information is available on biological activity of flavanone and its monohydroxy derivatives in relation to their physicochemical properties as spectral profiles, existence of protonated/deprotonated species under pH changes or interaction with Calf Thymus DNA. We devoted this work to research demonstrating differences in the physicochemical properties of the four flavanones: flavanone, 2'-hydroxyflavanone, 6-hydroxyflavanone and 7-hydroxyf"],"journal":["Molecules (Basel, Switzerland)"],"pagination":["E3049"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6749416"],"repository":["biostudies-literature"],"pubmed_title":["Position Impact of Hydroxy Groups on Spectral, Acid-Base Profiles and DNA Interactions of Several Monohydroxy Flavanones."],"pmcid":["PMC6749416"],"pubmed_authors":["Pilo M","Blazinska P","Korolevich VM","Lodyga-Chruscinska E","Cheshchevik VT","Kowalska-Baron A","Zucca A"],"additional_accession":[]},"is_claimable":false,"name":"Position Impact of Hydroxy Groups on Spectral, Acid-Base Profiles and DNA Interactions of Several Monohydroxy Flavanones.","description":"Structure-related biological activities of flavanones are still considered largely unexplored. Since they exhibit various medicinal activities, it is intriguing to enter deeper into their chemical structures, electronic transitions or interactions with some biomolecules in order to find properties that allow us to better understand their effects. Little information is available on biological activity of flavanone and its monohydroxy derivatives in relation to their physicochemical properties as spectral profiles, existence of protonated/deprotonated species under pH changes or interaction with Calf Thymus DNA. We devoted this work to research demonstrating differences in the physicochemical properties of the four flavanones: flavanone, 2'-hydroxyflavanone, 6-hydroxyflavanone and 7-hydroxyf","dates":{"release":"2019-01-01T00:00:00Z","publication":"2019 Aug","modification":"2025-04-22T19:19:11.419Z","creation":"2019-10-11T07:06:49Z"},"accession":"S-EPMC6749416","cross_references":{"pubmed":["31443449"],"doi":["10.3390/molecules24173049"]}}