Matuszczak B

References (5)

Title : Novel thiazolopyridine derivatives of diflapolin as dual sEH\/FLAP inhibitors with improved solubility - Schoenthaler_2023_Bioorg.Chem_139_106685
Author(s) : Schoenthaler M , Waltl L , Hasenoehrl T , Seher D , Lutz A , Aulinger L , Temml V , Konig S , Siller A , Braun DE , Garscha U , Werz O , Schuster D , Schennach H , Koeberle A , Matuszczak B
Ref : Bioorg Chem , 139 :106685 , 2023
Abstract : Schoenthaler_2023_Bioorg.Chem_139_106685
ESTHER : Schoenthaler_2023_Bioorg.Chem_139_106685
PubMedSearch : Schoenthaler_2023_Bioorg.Chem_139_106685
PubMedID: 37418786

Title : Synthesis and structure-activity relationships for some novel diflapolin derivatives with benzimidazole subunit - Vieider_2022_J.Enzyme.Inhib.Med.Chem_37_1752
Author(s) : Vieider L , Zoeller E , Romp E , Schoenthaler M , Hernandez-Olmos V , Temml V , Hasenoehrl T , Schuster D , Werz O , Garscha U , Matuszczak B
Ref : J Enzyme Inhib Med Chem , 37 :1752 , 2022
Abstract : Vieider_2022_J.Enzyme.Inhib.Med.Chem_37_1752
ESTHER : Vieider_2022_J.Enzyme.Inhib.Med.Chem_37_1752
PubMedSearch : Vieider_2022_J.Enzyme.Inhib.Med.Chem_37_1752
PubMedID: 36124840

Title : Synthesis, Biological Evaluation and Structure-Activity Relationships of Diflapolin Analogues as Dual sEH\/FLAP Inhibitors - Vieider_2019_ACS.Med.Chem.Lett_10_62
Author(s) : Vieider L , Romp E , Temml V , Fischer J , Kretzer C , Schoenthaler M , Taha A , Hernandez-Olmos V , Sturm S , Schuster D , Werz O , Garscha U , Matuszczak B
Ref : ACS Med Chem Lett , 10 :62 , 2019
Abstract : Vieider_2019_ACS.Med.Chem.Lett_10_62
ESTHER : Vieider_2019_ACS.Med.Chem.Lett_10_62
PubMedSearch : Vieider_2019_ACS.Med.Chem.Lett_10_62
PubMedID: 30655948

Title : Discovery of the first dual inhibitor of the 5-lipoxygenase-activating protein and soluble epoxide hydrolase using pharmacophore-based virtual screening - Temml_2017_Sci.Rep_7_42751
Author(s) : Temml V , Garscha U , Romp E , Schubert G , Gerstmeier J , Kutil Z , Matuszczak B , Waltenberger B , Stuppner H , Werz O , Schuster D
Ref : Sci Rep , 7 :42751 , 2017
Abstract : Temml_2017_Sci.Rep_7_42751
ESTHER : Temml_2017_Sci.Rep_7_42751
PubMedSearch : Temml_2017_Sci.Rep_7_42751
PubMedID: 28218273

Title : On the prodrug potential of novel aldose reductase inhibitors with diphenylmethyleneaminooxycarboxylic acid structure - Rakowitz_2002_Eur.J.Pharm.Sci_15_11
Author(s) : Rakowitz D , Matuszczak B , Gritsch S , Hofbauer P , Krassnigg A , Costantino L
Ref : Eur J Pharm Sci , 15 :11 , 2002
Abstract : Rakowitz_2002_Eur.J.Pharm.Sci_15_11
ESTHER : Rakowitz_2002_Eur.J.Pharm.Sci_15_11
PubMedSearch : Rakowitz_2002_Eur.J.Pharm.Sci_15_11
PubMedID: 11803127