An intelligent persistent luminescence nanoplatform with high-efficiency O2 utilization for continuous hypoxic tumors treatment

P Lin, J Shi, L Ming, Y Sheng, L Song, M Hong… - Chemical Engineering …, 2022 - Elsevier
Hypoxia, which emerges in most solid tumors, significantly restricts therapeutic effect during
treatment. To date, many smart nanoparticles that continuously generate O 2 have been …

Sulphonamides incorporating 1, 3, 5-triazine structural motifs show antioxidant, acetylcholinesterase, butyrylcholinesterase, and tyrosinase inhibitory profile

N Lolak, M Boga, M Tuneg, G Karakoc… - Journal of enzyme …, 2020 - Taylor & Francis
A series of 16 novel benzenesulfonamides incorporating 1, 3, 5-triazine moieties substituted
with aromatic amines, dimethylamine, morpholine and piperidine were investigated. These …

[HTML][HTML] Tumor associated carbonic anhydrase inhibitors: rational approaches, design strategies, structure activity relationship and mechanistic insights

SG Nerella, PS Thacker, M Arifuddin… - European Journal of …, 2024 - Elsevier
The emergence of tumor-associated human carbonic anhydrases (hCA) as promising
therapeutic targets has urged rigorous research into the development of potent and selective …

An overview of carbohydrate-based carbonic anhydrase inhibitors

D Cuffaro, E Nuti, A Rossello - Journal of Enzyme Inhibition and …, 2020 - Taylor & Francis
Carbonic anhydrases (CAs) are metalloenzymes responsible for the reversible hydration of
carbon dioxide to bicarbonate, a fundamental reaction involved in various physiological and …

Modulating the efficacy of carbonic anhydrase inhibitors through fluorine substitution

E Berrino, B Michelet, A Martin‐Mingot… - Angewandte Chemie …, 2021 - Wiley Online Library
The insertion of fluorine atoms and/or fluoroalkyl groups can lead to many beneficial effects
in biologically active molecules, such as enhanced metabolic stability, bioavailability …

Binding site comparison for coumarin inhibitors and amine/amino acid activators of human carbonic anhydrases

A Petreni, SM Osman, FA Alasmary… - European Journal of …, 2021 - Elsevier
The first structural analysis comparing the binding mode to the target carbonic anhydrases
(CAs, EC 4.2. 1.1) of two opposite classes of modulators is presented here: coumarin …

New Hybrids of 4-Amino-2,3-polymethylene-quinoline and p-Tolylsulfonamide as Dual Inhibitors of Acetyl- and Butyrylcholinesterase and Potential Multifunctional …

GF Makhaeva, NV Kovaleva, NP Boltneva… - Molecules, 2020 - mdpi.com
New hybrid compounds of 4-amino-2, 3-polymethylene-quinoline containing different sizes
of the aliphatic ring and linked to p-tolylsulfonamide with alkylene spacers of increasing …

Aromatic sulfonamides including a sulfonic acid tail: new membrane impermeant carbonic anhydrase inhibitors for targeting selectively the cancer-associated isoforms

S Giovannuzzi, M D'Ambrosio, C Luceri… - International Journal of …, 2021 - mdpi.com
We report here a new drug design strategy for producing membrane-impermeant carbonic
anhydrase (CA; EC 4.2. 1.1) inhibitors selectively targeting the tumor-associated, membrane …

Design and synthesis of sulfonamides incorporating a biotin moiety: Carbonic anhydrase inhibitory effects, antiproliferative activity and molecular modeling studies

P Begines, A Bonardi, A Nocentini, P Gratteri… - Bioorganic & Medicinal …, 2023 - Elsevier
Sulfonamides constitute an important class of classical carbonic anhydrase (CA, EC 4.2. 1.1)
inhibitors. Herein we have accomplished the conjugation of biotin with an ample number of …

The management of glaucoma and macular degeneration

CT Supuran - Expert Opinion on Therapeutic Patents, 2019 - Taylor & Francis
Glaucoma [1-8] and macular degeneration [9-11] are among the ophthalmologic diseases
increasingly affecting the aging population worldwide. It is estimated that around 76 million …