Publication:
Newly synthesized piperazine derivatives as tyrosinase inhibitors: in vitro and in silico studies

dc.contributor.authorERDEM, SAFİYE
dc.contributor.authorsDokuzparmak C., Oz Tuncay F., Basoglu Ozdemir S., Kurnaz B., Demir I., Colak A., Sag Erdem S., Yildirim N.
dc.date.accessioned2022-03-23T11:41:29Z
dc.date.available2022-03-23T11:41:29Z
dc.date.issued2022
dc.description.abstractIn this study, a series of new organic compounds with piperazine as a fundamental skeleton was synthesized and evaluated for their tyrosinase inhibitory potentials by in vitro and in silico studies. The in vitro studies have shown that compounds 10a and 10b bearing 1,2,4, triazole nucleus could be considered potent tyrosinase inhibitors with IC50 values of 31.2 ± 0.7 and 30.7 ± 0.2 µM, respectively. 10b (Ki = 9.54 µM, mixed type inhibition) with the lowest IC50 value among derivatives was selected to determine kinetic constants and inhibition types. Furthermore, molecular docking analysis was performed for all compounds and it was observed that 4b, 5a, 4c, and 10b showed promising inhibitory effect on tyrosinase activity. Based on docking results, ADME predictions and in vitro studies, 10b might be considered suitable oral drug candidates for further studies. © 2022, Iranian Chemical Society.
dc.identifier.doi10.1007/s13738-021-02487-3
dc.identifier.issn1735207X
dc.identifier.urihttps://hdl.handle.net/11424/254667
dc.language.isoeng
dc.publisherSpringer Science and Business Media Deutschland GmbH
dc.relation.ispartofJournal of the Iranian Chemical Society
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectMolecular docking
dc.subjectPiperazine
dc.subjectTriazole
dc.subjectTyrosinase inhibitor
dc.titleNewly synthesized piperazine derivatives as tyrosinase inhibitors: in vitro and in silico studies
dc.typearticle
dspace.entity.typePublication
local.avesis.id638eec5a-b4e3-48d0-a8ce-0eed030bc87c
local.import.packageSS28
local.import.sourceScopus
local.indexed.atSCOPUS
oaire.citation.titleJournal of the Iranian Chemical Society
relation.isAuthorOfPublication99f2f09c-7e48-402f-9bb9-ccdd73c27ec2
relation.isAuthorOfPublication.latestForDiscovery99f2f09c-7e48-402f-9bb9-ccdd73c27ec2

Files

Collections