Caliskan K

References (3)

Title : Potent soluble epoxide hydrolase inhibitors based on thiazole-5-carboxamide structure with imidazolidinone moiety as a secondary pharmacophore - Lengerli_2025_Bioorg.Chem_163_108644
Author(s) : Lengerli D , Koc B , Jordan PM , Caliskan K , Caliskan B , Werz O , Banoglu E
Ref : Bioorg Chem , 163 :108644 , 2025
Abstract :
PubMedSearch : Lengerli_2025_Bioorg.Chem_163_108644
PubMedID: 40466300

Title : Phenyl-benzyl-ureas with pyridazinone motif: Potent soluble epoxide hydrolase inhibitors with enhanced pharmacokinetics and efficacy in a paclitaxel-induced neuropathic pain model - Lengerli_2025_Eur.J.Med.Chem_290_117510
Author(s) : Lengerli D , Bakht A , Caliskan K , Dahlke P , Bal NB , Jordan PM , Caliskan B , Werz O , Banoglu E
Ref : Eur Journal of Medicinal Chemistry , 290 :117510 , 2025
Abstract :
PubMedSearch : Lengerli_2025_Eur.J.Med.Chem_290_117510
PubMedID: 40101448
Gene_locus related to this paper: human-EPHX2

Title : Harnessing structure-activity relationships to repurpose the FLAP inhibitor BRP-7 into potent and selective sEH inhibitors - Caliskan_2025_Bioorg.Chem_165_108997
Author(s) : Caliskan K , Karatas M , Jordan PM , Caliskan B , Werz O , Banoglu E
Ref : Bioorg Chem , 165 :108997 , 2025
Abstract :
PubMedSearch : Caliskan_2025_Bioorg.Chem_165_108997
PubMedID: 40974655
Gene_locus related to this paper: human-EPHX2