| Structure-based discovery of substituted 4, 5′-bithiazoles as novel DNA gyrase inhibitors M Brvar, A Perdih, M Renko, G Anderluh, D Turk, T Solmajer Journal of medicinal chemistry 55 (14), 6413-6426, 2012 | 185 | 2012 |
| Recent advances in the synthesis of unnatural α-amino acids A Perdih, MS Dolenc Current Organic Chemistry 11 (9), 801-832, 2007 | 111 | 2007 |
| Discovery of novel benzene 1, 3-dicarboxylic acid inhibitors of bacterial MurD and MurE ligases by structure-based virtual screening approach A Perdih, A Kovač, G Wolber, D Blanot, S Gobec, T Solmajer Bioorganic & medicinal chemistry letters 19 (10), 2668-2673, 2009 | 83 | 2009 |
| In silico discovery of 2-amino-4-(2, 4-dihydroxyphenyl) thiazoles as novel inhibitors of DNA gyrase B M Brvar, A Perdih, M Oblak, LP Mašič, T Solmajer Bioorganic & Medicinal Chemistry Letters 20 (3), 958-962, 2010 | 80 | 2010 |
| Recent developments of DNA poisons-human DNA topoisomerase IIα inhibitors-as anticancer agents B Pogorelcnik, A Perdih, T Solmajer Current pharmaceutical design 19 (13), 2474-2488, 2013 | 76 | 2013 |
| Binding free energy calculations of N-sulphonyl-glutamic acid inhibitors of MurD ligase A Perdih, U Bren, T Solmajer Journal of molecular modeling 15, 983-996, 2009 | 69 | 2009 |
| Targeted molecular dynamics simulation studies of binding and conformational changes in E. coli MurD A Perdih, M Kotnik, M Hodoscek, T Solmajer PROTEINS: Structure, Function, and Bioinformatics 68 (1), 243-254, 2007 | 68 | 2007 |
| Recent advances in the development of catalytic inhibitors of human DNA topoisomerase IIα as novel anticancer agents B Pogorelcnik, A Perdih, T Solmajer Current medicinal chemistry 20 (5), 694-709, 2013 | 63 | 2013 |
| The application of Freidinger lactams and their analogs in the design of conformationally constrained peptidomimetics A Perdih, D Kikelj Current medicinal chemistry 13 (13), 1525-1556, 2006 | 61 | 2006 |
| In silico discovery and biophysical evaluation of novel 5-(2-hydroxybenzylidene) rhodanine inhibitors of DNA gyrase B M Brvar, A Perdih, V Hodnik, M Renko, G Anderluh, R Jerala, T Solmajer Bioorganic & medicinal chemistry 20 (8), 2572-2580, 2012 | 58 | 2012 |
| Small molecule antagonists of integrin receptors A Perdih, M Sollner Dolenc Current medicinal chemistry 17 (22), 2371-2392, 2010 | 55 | 2010 |
| Flavonoids and cinnamic acid esters as inhibitors of fungal 17β-hydroxysteroid dehydrogenase: A synthesis, QSAR and modelling study M Sova, A Perdih, M Kotnik, K Kristan, TL Rižner, T Solmajer, S Gobec Bioorganic & medicinal chemistry 14 (22), 7404-7418, 2006 | 52 | 2006 |
| 1, 3‐Diamine‐Derived Bifunctional Organocatalyst Prepared from Camphor S Ričko, J Svete, B Štefane, A Perdih, A Golobič, A Meden, U Grošelj Advanced Synthesis & Catalysis 358 (23), 3786-3796, 2016 | 50 | 2016 |
| Benzene-1, 3-dicarboxylic acid 2, 5-dimethylpyrrole derivatives as multiple inhibitors of bacterial Mur ligases (MurC–MurF) A Perdih, M Hrast, H Barreteau, S Gobec, G Wolber, T Solmajer Bioorganic & medicinal chemistry 22 (15), 4124-4134, 2014 | 43 | 2014 |
| 4,6-Substituted-1,3,5-triazin-2(1H)-ones as monocyclic catalytic inhibitors of human DNA topoisomerase IIα targeting the ATP binding site B Pogorelčnik, M Janežič, I Sosič, S Gobec, T Solmajer, A Perdih Bioorganic & medicinal chemistry 23 (15), 4218-4229, 2015 | 42 | 2015 |
| Discovery of Mono‐ and Disubstituted 1H‐Pyrazolo[3,4]pyrimidines and 9H‐Purines as Catalytic Inhibitors of Human DNA Topoisomerase IIα B Pogorelčnik, M Brvar, B Žegura, M Filipič, T Solmajer, A Perdih ChemMedChem 10 (2), 345-359, 2015 | 42 | 2015 |
| Recent advances in the synthesis of unnatural α-amino acids-An updated version A Perdih, M Sollner Dolenc Current Organic Chemistry 15 (22), 3750-3799, 2011 | 39 | 2011 |
| Discovery of the first inhibitors of bacterial enzyme D-aspartate ligase from Enterococcus faecium (Aslfm) V Škedelj, A Perdih, M Brvar, A Kroflič, V Dubbée, V Savage, AJ O'Neill, ... European Journal of Medicinal Chemistry 67, 208-220, 2013 | 37 | 2013 |
| Farmacevtska kemija III: Vaje in seminarji M Anderluh, J Mravljak, A Perdih, M Sova, S Pečar Fakulteta za farmacijo, 2010 | 37 | 2010 |
| Monocyclic 4-amino-6-(phenylamino)-1, 3, 5-triazines as inhibitors of human DNA topoisomerase IIα B Pogorelčnik, M Brvar, I Zajc, M Filipič, T Solmajer, A Perdih Bioorganic & Medicinal Chemistry Letters 24 (24), 5762-5768, 2014 | 33 | 2014 |
