Sulfonamide drugs: Structure, antibacterial property, toxicity, and biophysical interactions

A Ovung, J Bhattacharyya - Biophysical reviews, 2021 - Springer
Sulfonamide (or sulphonamide) functional group chemistry (SN) forms the basis of several
groups of drug. In vivo sulfonamides exhibit a range of pharmacological activities, such as …

[HTML][HTML] Targeting matrix metalloproteinases in cancer: bringing new life to old ideas

J Cathcart, A Pulkoski-Gross, J Cao - Genes & diseases, 2015 - Elsevier
Since the identification of matrix metalloproteinases (MMPs), a family of zinc-dependent
endopeptidases, as being a driving factor for cancer progression and patient prognosis …

Synthesis of sulfonamide and their synthetic and therapeutic applications: Recent advances

S Mondal, S Malakar - Tetrahedron, 2020 - Elsevier
A sulfonamide is a functional group that is the basis of several sulfa drugs and thereby are
very much important scaffolds in medicinal as well as in synthetic organic chemistry …

Sulfa and trimethoprim-like drugs–antimetabolites acting as carbonic anhydrase, dihydropteroate synthase and dihydrofolate reductase inhibitors

C Capasso, CT Supuran - Journal of enzyme inhibition and …, 2014 - Taylor & Francis
Recent advances in microbial genomics, synthetic organic chemistry and X-ray
crystallography provided opportunities to identify novel antibacterial targets for the …

Bacterial, fungal and protozoan carbonic anhydrases as drug targets

C Capasso, CT Supuran - Expert opinion on therapeutic targets, 2015 - Taylor & Francis
Introduction: The carbonic anhydrases (CAs, EC 4.2. 1.1), a group of ubiquitously expressed
metalloenzymes, are involved in numerous physiological and pathological processes, as …

Structure, function and applications of carbonic anhydrase isozymes

MI Hassan, B Shajee, A Waheed, F Ahmad… - Bioorganic & medicinal …, 2013 - Elsevier
The carbonic anhydrases enzymes (CAs, EC 4.2. 1.1) are zinc containing metalloproteins,
which efficiently catalyse the reversible conversion of carbon dioxide to bicarbonate and …

Vinyl sulfones: Synthetic preparations and medicinal chemistry applications

DC Meadows, J Gervay‐Hague - Medicinal research reviews, 2006 - Wiley Online Library
Vinyl sulfones have long been known for their synthetic utility in organic chemistry, easily
participating in 1, 4‐addition reactions and cycloaddition reactions. This functional group …

The development of BTK inhibitors: a five-year update

B Tasso, A Spallarossa, E Russo, C Brullo - Molecules, 2021 - mdpi.com
Bruton's tyrosine kinase (BTK) represented, in the past ten years, an important target for the
development of new therapeutic agents that could be useful for cancer and autoimmune …

Pd-Catalyzed Conversion of Aryl Iodides to Sulfonyl Fluorides Using SO2 Surrogate DABSO and Selectfluor

AL Tribby, I Rodríguez, S Shariffudin… - The Journal of organic …, 2017 - ACS Publications
A one-pot Pd-catalyzed conversion of aryl iodide to aryl sulfonyl fluorides using DABSO and
Selectfluor has been developed generating aryl sulfonyl fluorides in good to excellent yields …

Synthesis, Antimicrobial, Anti-Virulence and Anticancer Evaluation of New 5(4H)-Oxazolone-Based Sulfonamides

AJ Almalki, TS Ibrahim, ES Taher, MFA Mohamed… - Molecules, 2022 - mdpi.com
Since the synthesis of prontosil the first prodrug shares their chemical moiety, sulfonamides
exhibit diverse modes of actions to serve as antimicrobials, diuretics, antidiabetics, and other …