| Unraveling the Structure–Affinity Relationship between Cucurbit[n]urils (n = 7, 8) and Cationic Diamondoids D Sigwalt, M Sekutor, L Cao, PY Zavalij, J Hostas, H Ajani, P Hobza, ... Journal of the American Chemical Society 139 (8), 3249-3258, 2017 | 95 | 2017 |
| Malonate-based inhibitors of mammalian serine racemase: kinetic characterization and structure-based computational study B Vorlová, D Nachtigallová, J Jirásková-Vaníčková, H Ajani, P Jansa, ... European journal of medicinal chemistry 89, 189-197, 2015 | 62 | 2015 |
| Synthesis, structural characterization, docking, lipophilicity and cytotoxicity of 1-[(1R)-1-(6-fluoro-1, 3-benzothiazol-2-yl) ethyl]-3-alkyl carbamates, novel … V Pejchal, Š Štěpánková, M Pejchalová, K Královec, R Havelek, ... Bioorganic & Medicinal Chemistry 24 (7), 1560-1572, 2016 | 43 | 2016 |
| Discovery of N2-(4-Amino-cyclohexyl)-9-cyclopentyl-N6-(4-morpholin-4-ylmethyl-phenyl)-9H-purine-2,6-diamine as a Potent FLT3 Kinase Inhibitor for Acute … T Gucky, E Reznickova, T Radošová Muchová, R Jorda, Z Klejova, ... Journal of Medicinal Chemistry 61 (9), 3855-3869, 2018 | 41 | 2018 |
| Explicit treatment of active-site waters enhances quantum mechanical/implicit solvent scoring: Inhibition of CDK2 by new pyrazolo [1, 5-a] pyrimidines M Hylsová, B Carbain, J Fanfrlík, L Musilová, S Haldar, C Köprülüoğlu, ... European Journal of Medicinal Chemistry 126, 1118-1128, 2017 | 38 | 2017 |
| Synthesis and structure–activity relationship of potent, selective and orally active anthranilamide-based factor Xa inhibitors: Application of weakly basic sulfoximine group as … V Pandya, M Jain, G Chakrabarti, H Soni, B Parmar, B Chaugule, J Patel, ... European journal of medicinal chemistry 58, 136-152, 2012 | 37 | 2012 |
| A Nexus between Theory and Experiment: Non‐Empirical Quantum Mechanical Computational Methodology Applied to Cucurbit[n]uril⋅Guest Binding Interactions J Hostaš, D Sigwalt, M Šekutor, H Ajani, M Dubecký, J Řezáč, PY Zavalij, ... Chemistry–A European Journal 22 (48), 17226-17238, 2016 | 35 | 2016 |
| Characteristics of a σ-hole and the nature of a halogen bond MH Kolář, P Deepa, H Ajani, A Pecina, P Hobza Halogen Bonding II: Impact on Materials Chemistry and Life Sciences, 1-25, 2015 | 34 | 2015 |
| Evaluation of antidiabetic effect of methanolic extract of Inula racemosa root in rats HB Ajani, HP Patel, GB Shah, SR Acharya, SK Shah Pharmacologyonline 3, 118-129, 2009 | 23 | 2009 |
| Superior performance of the SQM/COSMO scoring functions in native pose recognition of diverse protein–ligand complexes in cognate docking H Ajani, A Pecina, SM Eyrilmez, J Fanfrlík, S Haldar, J Řezáč, P Hobza, ... ACS omega 2 (7), 4022-4029, 2017 | 22 | 2017 |
| IDD388 polyhalogenated derivatives as probes for an improved structure-based selectivity of AKR1B10 inhibitors A Cousido-Siah, FX Ruiz, J Fanfrlik, J Gimenez-Dejoz, A Mitschler, ... ACS Chemical Biology 11 (10), 2693-2705, 2016 | 20 | 2016 |
| Tetrahydropyrazolo [1, 5-a] pyridine-fused steroids and their in vitro biological evaluation in prostate cancer R Jorda, SMM Lopes, E Řezníčková, H Ajani, AV Pereira, CSB Gomes, ... European Journal of Medicinal Chemistry 178, 168-176, 2019 | 18 | 2019 |
| Halogen Bonding II: Impact on Materials Chemistry and Life Sciences H Ajani Springer, 2015 | 14 | 2015 |
| Imidazo[1,2‐c]pyrimidin‐5(6H)‐one as a novel core of cyclin‐dependent kinase 2 inhibitors: Synthesis, activity measurement, docking, and quantum mechanical … H Ajani, J Jansa, C Köprülüoğlu, P Hobza, V Kryštof, A Lyčka, M Lepsik Journal of Molecular Recognition 31 (9), e2720, 2018 | 13 | 2018 |
| 3H-Pyrazolo[4,3-f]quinoline-Based Kinase Inhibitors Inhibit the Proliferation of Acute Myeloid Leukemia Cells In Vivo N Dayal, E Reznickova, DE Hernandez, M Perina, S Torregrosa-Allen, ... Journal of Medicinal Chemistry 64 (15), 10981-10996, 2021 | 12 | 2021 |
| The synthesis and cholinesterase inhibitory activities of solasodine analogues with seven-membered F ring U Kiełczewska, R Jorda, G Gonzalez, JW Morzycki, H Ajani, K Svrčková, ... The journal of steroid biochemistry and molecular biology 205, 105776, 2021 | 12 | 2021 |
| Polysubstituted Pyrimidines as mPGES‐1 Inhibitors: Discovery of Potent Inhibitors of PGE2 Production with Strong Anti‐inflammatory Effects in Carrageenan … F Kalčic, V Kolman, H Ajani, Z Zídek, Z Janeba ChemMedChem 15 (15), 1398-1407, 2020 | 11 | 2020 |
| Activity of 2, 6, 9-trisubstituted purines as potent PDGFRα kinase inhibitors with antileukaemic activity E Řezníčková, T Gucký, V Kováčová, H Ajani, R Jorda, V Kryštof European Journal of Medicinal Chemistry 182, 111663, 2019 | 10 | 2019 |
| Activity of 2, 6, 9-trisubstituted purines as potent PDGFR alpha kinase inhibitors with antileukaemic activity E Reznickova, T Gucky, V Kovacova, H Ajani, R Jorda, V Krystof European Journal of Medicinal Chemistry 182, 2019 | 5 | 2019 |
| Optimization of norbornyl‐based carbocyclic nucleoside analogs as cyclin‐dependent kinase 2 inhibitors C Köprülüoğlu, M Dejmek, M Šála, H Ajani, H Hřebabecký, J Fanfrlík, ... Journal of Molecular Recognition 33 (8), e2842, 2020 | 2 | 2020 |
Martin LepsikInst. Org. Chem. Biochem., Czech Acad SciE-mailová adresa ověřena na: uochb.cas.cz
