Progress in the development of human carbonic anhydrase inhibitors and their pharmacological applications: Where are we today?

CB Mishra, M Tiwari, CT Supuran - Medicinal Research …, 2020 - Wiley Online Library
Abstract Carbonic anhydrases (CAs, EC 4.2. 1.1) are widely distributed metalloenzymes in
both prokaryotes and eukaryotes. They efficiently catalyze the reversible hydration of carbon …

Synthetic approaches and pharmaceutical applications of chloro-containing molecules for drug discovery: A critical review

WY Fang, L Ravindar, KP Rakesh… - European Journal of …, 2019 - Elsevier
At present more than 250 FDA approved chlorine containing drugs were available in the
market and many pharmaceutically important drug candidates in pre-clinical trials. Thus, it is …

New Benzimidazole-, 1,2,4-Triazole-, and 1,3,5-Triazine-Based Derivatives as Potential EGFRWT and EGFRT790M Inhibitors: Microwave-Assisted Synthesis …

HE Hashem, AEGE Amr, ES Nossier, MM Anwar… - ACS …, 2022 - ACS Publications
A new series of benzimidazole, 1, 2, 4-triazole, and 1, 3, 5-triazine derivatives were
designed and synthesized using a microwave irradiation synthetic approach utilizing 2 …

Recent advances in the biological activity of s-triazine core compounds

D Maliszewski, D Drozdowska - Pharmaceuticals, 2022 - mdpi.com
An effective strategy for successful chemotherapy relies on creating compounds with high
selectivity against cancer cells compared to normal cells and relatively low cytotoxicity. One …

Recent updates on 1, 2, 3‐, 1, 2, 4‐, and 1, 3, 5‐triazine hybrids (2017–present): The anticancer activity, structure–activity relationships, and mechanisms of action

G Dong, Y Jiang, F Zhang, F Zhu, J Liu… - Archiv der …, 2023 - Wiley Online Library
Cancer is one of the leading causes of death across the world, and the prevalence and
mortality rates of cancer will continue to grow. Chemotherapeutics play a critical role in …

4-(3-Alkyl/benzyl-guanidino) benzenesulfonamides as selective carbonic anhydrase VII inhibitors

M Abdoli, S Giovannuzzi, CT Supuran… - Journal of Enzyme …, 2022 - Taylor & Francis
The treatment of chronic neuropathic pain remains one of the most challenging of all
neurological diseases and very much an art. There exists no consensus for the optimal …

Unraveling the mechanism of carbonic anhydrase IX inhibition by alkaloids from Ruta chalepensis: A synergistic analysis of in vitro and in silico data

HA Alqhtani, SI Othman, FFA Alkhayl, NG Altoom… - Biochemical and …, 2024 - Elsevier
Due to the pivotal role of carbonic anhydrase IX (CA IX) in pathological conditions, there's a
pressing need for novel inhibitors to improve patient outcomes and clinical management …

Synthetic and pharmacological developments in the hybrid s-triazine moiety: A review

D Bareth, S Jain, J Kumawat, D Kishore, J Dwivedi… - Bioorganic …, 2024 - Elsevier
This article summarizes the most recent advancements in the synthetic and pharmacological
approaches along with the structure activity relationship towards the s-triazine and its …

Continued exploration and tail approach synthesis of benzenesulfonamides containing triazole and dual triazole moieties as carbonic anhydrase I, II, IV and IX …

L Vats, R Kumar, S Bua, A Nocentini, P Gratteri… - European Journal of …, 2019 - Elsevier
A library of twenty two novel 1, 2, 3-triazole benzenesulfonamides incorporating
thiosemicarbazide, 5 (4 H)-thione-1, 2, 4-triazole and variously substituted phenacyl …

Synthesis of novel benzenesulfonamide bearing 1, 2, 3-triazole linked hydroxy-trifluoromethylpyrazolines and hydrazones as selective carbonic anhydrase isoforms IX …

V Sharma, R Kumar, S Bua, CT Supuran… - Bioorganic …, 2019 - Elsevier
A series of twenty four hydroxy-trifluoromethylpyrazoline-carbonyl-1, 2, 3-triazoles and four
hydrazones bearing benzenesulfonamide moieties was obtained by condensation of …