Moi D - Search Results

1

Synthesis and evaluation of antioxidant and antiproliferative activity of 2-arylbenzimidazoles.

Baldisserotto A, Demurtas M, Lampronti I, Tacchini M, Moi D, Balboni G, Pacifico S, Vertuani S, Manfredini S, Onnis V. Baldisserotto A, et al. Among authors: moi d. Bioorg Chem. 2020 Jan;94:103396. doi: 10.1016/j.bioorg.2019.103396. Epub 2019 Oct 24. Bioorg Chem. 2020. PMID: 31677860

2

Recent Advances in SARS-CoV-2 Main Protease Inhibitors: From Nirmatrelvir to Future Perspectives.

Citarella A, Dimasi A, Moi D, Passarella D, Scala A, Piperno A, Micale N. Citarella A, et al. Among authors: moi d. Biomolecules. 2023 Sep 2;13(9):1339. doi: 10.3390/biom13091339. Biomolecules. 2023. PMID: 37759739 Free PMC article. Review.

3

Discovery of thiazolin-4-one-based aromatic sulfamates as a new class of carbonic anhydrase isoforms I, II, IV, and IX inhibitors.

Nocentini A, Moi D, Balboni G, Onnis V, Supuran CT. Nocentini A, et al. Among authors: moi d. Bioorg Chem. 2018 Apr;77:293-299. doi: 10.1016/j.bioorg.2018.01.023. Epub 2018 Jan 31. Bioorg Chem. 2018. PMID: 29421705

4

Synthesis and biological evaluation of novel pyrazoline-based aromatic sulfamates with potent carbonic anhydrase isoforms II, IV and IX inhibitory efficacy.

Nocentini A, Moi D, Balboni G, Salvadori S, Onnis V, Supuran CT. Nocentini A, et al. Among authors: moi d. Bioorg Chem. 2018 Apr;77:633-639. doi: 10.1016/j.bioorg.2018.02.021. Epub 2018 Feb 23. Bioorg Chem. 2018. PMID: 29502024

5

Benzofuran hydrazones as potential scaffold in the development of multifunctional drugs: Synthesis and evaluation of antioxidant, photoprotective and antiproliferative activity.

Baldisserotto A, Demurtas M, Lampronti I, Moi D, Balboni G, Vertuani S, Manfredini S, Onnis V. Baldisserotto A, et al. Among authors: moi d. Eur J Med Chem. 2018 Aug 5;156:118-125. doi: 10.1016/j.ejmech.2018.07.001. Epub 2018 Jul 2. Eur J Med Chem. 2018. PMID: 30006157

6

Indole derivatives as multifunctional drugs: Synthesis and evaluation of antioxidant, photoprotective and antiproliferative activity of indole hydrazones.

Demurtas M, Baldisserotto A, Lampronti I, Moi D, Balboni G, Pacifico S, Vertuani S, Manfredini S, Onnis V. Demurtas M, et al. Among authors: moi d. Bioorg Chem. 2019 Apr;85:568-576. doi: 10.1016/j.bioorg.2019.02.007. Epub 2019 Feb 10. Bioorg Chem. 2019. PMID: 30825715

7

Synthesis and in vitro evaluation of piperazinyl-ureido sulfamates as steroid sulfatase inhibitors.

Moi D, Foster PA, Rimmer LG, Jaffri A, Deplano A, Balboni G, Onnis V, Potter BVL. Moi D, et al. Eur J Med Chem. 2019 Nov 15;182:111614. doi: 10.1016/j.ejmech.2019.111614. Epub 2019 Aug 12. Eur J Med Chem. 2019. PMID: 31422224

8

Structure-activity relationship with pyrazoline-based aromatic sulfamates as carbonic anhydrase isoforms I, II, IX and XII inhibitors: Synthesis and biological evaluation.

Moi D, Nocentini A, Deplano A, Balboni G, Supuran CT, Onnis V. Moi D, et al. Eur J Med Chem. 2019 Nov 15;182:111638. doi: 10.1016/j.ejmech.2019.111638. Epub 2019 Aug 22. Eur J Med Chem. 2019. PMID: 31472471

9

Sulfonamide/sulfamate switch with a series of piperazinylureido derivatives: Synthesis, kinetic and in silico evaluation as carbonic anhydrase isoforms I, II, IV, and IX inhibitors.

Nocentini A, Moi D, Deplano A, Osman SM, AlOthman ZA, Balboni G, Supuran CT, Onnis V. Nocentini A, et al. Among authors: moi d. Eur J Med Chem. 2020 Jan 15;186:111896. doi: 10.1016/j.ejmech.2019.111896. Epub 2019 Nov 21. Eur J Med Chem. 2020. PMID: 31784185

10

Appliance of the piperidinyl-hydrazidoureido linker to benzenesulfonamide compounds: Synthesis, in vitro and in silico evaluation of potent carbonic anhydrase II, IX and XII inhibitors.

Moi D, Nocentini A, Deplano A, Osman SM, AlOthman ZA, Piras V, Balboni G, Supuran CT, Onnis V. Moi D, et al. Bioorg Chem. 2020 May;98:103728. doi: 10.1016/j.bioorg.2020.103728. Epub 2020 Mar 14. Bioorg Chem. 2020. PMID: 32182519

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