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Alessandro Bonardi
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Enhancement of the tail hydrophobic interactions within the carbonic anhydrase IX active site via structural extension: Design and synthesis of novel N-substituted isatins-SLC …
WM Eldehna, MF Abo-Ashour, A Nocentini, RS El-Haggar, S Bua, ...
European journal of medicinal chemistry 162, 147-160, 2019
892019
Sulfonamide inhibitors of human carbonic anhydrases designed through a three-tails approach: improving ligand/isoform matching and selectivity of action
A Bonardi, A Nocentini, S Bua, J Combs, C Lomelino, J Andring, ...
Journal of medicinal chemistry 63 (13), 7422-7444, 2020
822020
Steroids interfere with human carbonic anhydrase activity by using alternative binding mechanisms
A Nocentini, A Bonardi, P Gratteri, B Cerra, A Gioiello, CT Supuran
Journal of Enzyme Inhibition and Medicinal Chemistry 33 (1), 1453-1459, 2018
792018
3-Hydrazinoisatin-based benzenesulfonamides as novel carbonic anhydrase inhibitors endowed with anticancer activity: Synthesis, in vitro biological evaluation and in silico …
MF Abo-Ashour, WM Eldehna, A Nocentini, A Bonardi, S Bua, HS Ibrahim, ...
European Journal of Medicinal Chemistry 184, 111768, 2019
672019
Dual-tail arylsulfone-based benzenesulfonamides differently match the hydrophobic and hydrophilic halves of human carbonic anhydrases active sites: Selective inhibitors for the …
HS Ibrahim, HA Allam, WR Mahmoud, A Bonardi, A Nocentini, P Gratteri, ...
European Journal of Medicinal Chemistry 152, 1-9, 2018
642018
Sulfonamide-based ring-fused analogues for CAN508 as novel carbonic anhydrase inhibitors endowed with antitumor activity: Design, synthesis, and in vitro biological evaluation
MA Said, WM Eldehna, A Nocentini, SH Fahim, A Bonardi, AA Elgazar, ...
European Journal of Medicinal Chemistry 189, 112019, 2020
522020
3-Methylthiazolo [3, 2-a] benzimidazole-benzenesulfonamide conjugates as novel carbonic anhydrase inhibitors endowed with anticancer activity: Design, synthesis, biological and …
AAM Alkhaldi, MM Al-Sanea, A Nocentini, WM Eldehna, ZM Elsayed, ...
European Journal of Medicinal Chemistry 207, 112745, 2020
512020
Structural investigations on coumarins leading to chromeno [4, 3-c] pyrazol-4-ones and pyrano [4, 3-c] pyrazol-4-ones: New scaffolds for the design of the tumor-associated …
A Bonardi, M Falsini, D Catarzi, F Varano, LDC Mannelli, B Tenci, ...
European Journal of Medicinal Chemistry 146, 47-59, 2018
512018
Inclusion of a 5-fluorouracil moiety in nitrogenous bases derivatives as human carbonic anhydrase IX and XII inhibitors produced a targeted action against MDA-MB-231 and T47D …
A Petreni, A Bonardi, C Lomelino, SM Osman, ZA ALOthman, ...
European Journal of Medicinal Chemistry 190, 112112, 2020
482020
2-Benzylpiperazine: A new scaffold for potent human carbonic anhydrase inhibitors. Synthesis, enzyme inhibition, enantioselectivity, computational and crystallographic studies …
N Chiaramonte, S Bua, M Ferraroni, A Nocentini, A Bonardi, G Bartolucci, ...
European Journal of Medicinal Chemistry 151, 363-375, 2018
472018
Novel 3-substituted coumarins as selective human carbonic anhydrase IX and XII inhibitors: Synthesis, biological and molecular dynamics analysis
MA Abdelrahman, HS Ibrahim, A Nocentini, WM Eldehna, A Bonardi, ...
European Journal of Medicinal Chemistry 209, 112897, 2021
452021
Synthesis, biological and molecular dynamics investigations with a series of triazolopyrimidine/triazole-based benzenesulfonamides as novel carbonic anhydrase inhibitors
MA Said, WM Eldehna, A Nocentini, A Bonardi, SH Fahim, S Bua, ...
European Journal of Medicinal Chemistry 185, 111843, 2020
432020
Selective Inhibition of Helicobacter pylori Carbonic Anhydrases by Carvacrol and Thymol Could Impair Biofilm Production and the Release of Outer Membrane …
R Grande, S Carradori, V Puca, I Vitale, A Angeli, A Nocentini, A Bonardi, ...
International journal of molecular sciences 22 (21), 11583, 2021
352021
The antibiotic furagin and its derivatives are isoform-selective human carbonic anhydrase inhibitors
A Pustenko, A Nocentini, P Gratteri, A Bonardi, I Vozny, R Žalubovskis, ...
Journal of Enzyme Inhibition and Medicinal Chemistry 35 (1), 1011-1020, 2020
322020
Benzoxaboroles: New Potent Inhibitors of the Carbonic Anhydrases of the Pathogenic Bacterium Vibrio cholerae
A Bonardi, A Nocentini, R Cadoni, S Del Prete, P Dumy, C Capasso, ...
ACS Medicinal Chemistry Letters 11 (11), 2277-2284, 2020
272020
N-Nitrosulfonamides as Carbonic Anhydrase Inhibitors: A Promising Chemotype for Targeting Chagas Disease and Leishmaniasis
A Bonardi, AB Vermelho, V da Silva Cardoso, MC de Souza Pereira, ...
ACS Medicinal Chemistry Letters 10 (4), 413-418, 2018
272018
Synthesis, biological evaluation and in silico studies with 4-benzylidene-2-phenyl-5 (4H)-imidazolone-based benzenesulfonamides as novel selective carbonic anhydrase IX …
WM Eldehna, MA Abdelrahman, A Nocentini, S Bua, ST Al-Rashood, ...
Bioorganic Chemistry 90, 103102, 2019
262019
Design and synthesis of benzothiazole-based SLC-0111 analogues as new inhibitors for the cancer-associated carbonic anhydrase isoforms IX and XII
T Al-Warhi, MM Elbadawi, A Bonardi, A Nocentini, AA Al-Karmalawy, ...
Journal of Enzyme Inhibition and Medicinal Chemistry 37 (1), 2635-2643, 2022
252022
Pharmaceutical strategies for preventing toxicity and promoting antioxidant and anti-inflammatory actions of bilirubin
A Nocentini, A Bonardi, S Pratesi, P Gratteri, C Dani, CT Supuran
Journal of Enzyme Inhibition and Medicinal Chemistry 37 (1), 487-501, 2022
242022
Novel benzenesulfonamides aryl and arylsulfone conjugates adopting tail/dual tail approaches: synthesis, carbonic anhydrase inhibitory activity and molecular modeling studies
AH Eldeeb, MF Abo-Ashour, A Angeli, A Bonardi, DS Lasheen, ...
European Journal of Medicinal Chemistry 221, 113486, 2021
222021
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