Recent advances in synthetic strategies and SAR of thiazolidin-4-one containing molecules in cancer therapeutics

A Sharma, D Sharma, N Saini, SV Sharma… - Cancer and Metastasis …, 2023 - Springer
Cancer is one of the life-threatening diseases accountable for millions of demises globally.
The inadequate effectiveness of the existing chemotherapy and its harmful effects has …

Carbonic anhydrases: An overview

A Nocentini, CT Supuran - Carbonic Anhydrases, 2019 - Elsevier
Abstract Carbonic anhydrases (CAs, EC 4.2. 1.1) catalyze the interconversion between CO 2
and bicarbonate as well as other hydrolytic reactions. Seven genetic families of CAs have …

Steroids interfere with human carbonic anhydrase activity by using alternative binding mechanisms

A Nocentini, A Bonardi, P Gratteri, B Cerra… - Journal of Enzyme …, 2018 - Taylor & Francis
Bile acids have been shown to inhibit human (h) carbonic anhydrases (CA, EC 4.2. 1.1)
along the gastrointestinal tract, including hCA II. The elucidation of the hormonal inhibition …

Development of benzene and benzothiazole-sulfonamide analogues as selective inhibitors of the tumor-associated carbonic anhydrase IX

S Manzoor, A Angeli, S Zara, S Carradori… - European Journal of …, 2022 - Elsevier
With an aim to develop novel potential antitumor agents, two series of benzene-and
benzothiazole-sulfonamide derivatives, acting as effective human carbonic anhydrase (hCA …

4-Hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms IX and XII showing hypoxia-enhanced …

A Nocentini, E Trallori, S Singh… - Journal of Medicinal …, 2018 - ACS Publications
Human carbonic anhydrases (CA, EC, 4.2. 1.1) IX and XII are overexpressed in cancer cells
as adaptive response to hypoxia and acidic conditions characteristic of many tumors. In …

Synthesis, biological and molecular dynamics investigations with a series of triazolopyrimidine/triazole-based benzenesulfonamides as novel carbonic anhydrase …

MA Said, WM Eldehna, A Nocentini, A Bonardi… - European Journal of …, 2020 - Elsevier
In the presented work, we report the design and synthesis of different new sets of
triazolopyrimidine-based (9a-d) and triazole-based (11a-h, 13a-c, 15a, b, 17a, b and 21a-g) …

Synthesis of novel isoindoline-1, 3-dione-based oximes and benzenesulfonamide hydrazones as selective inhibitors of the tumor-associated carbonic anhydrase IX

AM Alaa, AS El-Azab, MAA El-Enin, AA Almehizia… - Bioorganic …, 2018 - Elsevier
The synthesis, characterization and biological evaluation of a library of isoindoline-1, 3-
dione-based oximes and benzenesulfonamide hydrazones is disclosed. The set of …

Investigation on hydrazonobenzenesulfonamides as human carbonic anhydrase I, II, IX and XII inhibitors

D Moi, S Vittorio, A Angeli, G Balboni, CT Supuran… - Molecules, 2022 - mdpi.com
A small series of hydrazonobenzenesulfonamides was designed, synthesized and studied
for their human carbonic anhydrase (hCA) inhibitory activity. The synthesized compounds …

Bioisosteric development of multitarget nonsteroidal anti-inflammatory drug–carbonic anhydrases inhibitor hybrids for the management of rheumatoid arthritis

S Bua, L Lucarini, L Micheli, M Menicatti… - Journal of Medicinal …, 2019 - ACS Publications
Multitarget nonsteroidal anti-inflammatory drug (NSAID)–carbonic anhydrase inhibitor (CAI)
agents for the management of rheumatoid arthritis are reported. The evidence of the plasma …

Human carbonic anhydrases: tissue distribution, physiological role, and druggability

A Nocentini, WA Donald, CT Supuran - Carbonic anhydrases, 2019 - Elsevier
Fifteen different carbonic anhydrase (CA) isoforms have been identified and characterized in
human (h) so far, of which 12 are catalytically active and 3 lack activity (CA-related proteins) …