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Claudiu T. Supuran

University of Florence

ORCID: 0000-0003-4262-0323

Publishes on Enzyme function and inhibition, Synthesis and Catalytic Reactions, Cholinesterase and Neurodegenerative Diseases. 2.8k papers and 131.1k citations.

2.8kPublications
131.1kTotal Citations

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Top publicationsby citations

Natural products in drug discovery: advances and opportunities
Atanas G. Atanasov, Sergey B. Zotchev, Verena M. Dirsch et al.|Nature Reviews Drug Discovery|2021
Cited by 4.9kOpen Access

Natural products and their structural analogues have historically made a major contribution to pharmacotherapy, especially for cancer and infectious diseases. Nevertheless, natural products also present challenges for drug discovery, such as technical barriers to screening, isolation, characterization and optimization, which contributed to a decline in their pursuit by the pharmaceutical industry from the 1990s onwards. In recent years, several technological and scientific developments - including improved analytical tools, genome mining and engineering strategies, and microbial culturing advances - are addressing such challenges and opening up new opportunities. Consequently, interest in natural products as drug leads is being revitalized, particularly for tackling antimicrobial resistance. Here, we summarize recent technological developments that are enabling natural product-based drug discovery, highlight selected applications and discuss key opportunities.

Carbonic anhydrase inhibitors
Claudiu T. Supuran, Andrea Scozzafava, Angela Casini|Medicinal Research Reviews|2002
Cited by 1.4k

At least 14 different carbonic anhydrase (CA, EC 4.2.1.1) isoforms were isolated in higher vertebrates, where these zinc enzymes play crucial physiological roles. Some of these isozymes are cytosolic (CA I, CA II, CA III, CA VII), others are membrane-bound (CA IV, CA IX, CA XII, and CA XIV), CA V is mitochondrial and CA VI is secreted in saliva. Three acatalytic forms are also known, which are denominated CA related proteins (CARP), CARP VIII, CARP X, and CARP XI. Several important physiological and physio-pathological functions are played by many CA isozymes, which are strongly inhibited by aromatic and heterocyclic sulfonamides as well as inorganic, metal complexing anions. The catalytic and inhibition mechanisms of these enzymes are understood in detail, and this helped the design of potent inhibitors, some of which possess important clinical applications. The use of such enzyme inhibitors as antiglaucoma drugs will be discussed in detail, together with the recent developments that led to isozyme-specific and organ-selective inhibitors. A recent discovery is connected with the involvement of CAs and their sulfonamide inhibitors in cancer: several potent sulfonamide inhibitors inhibited the growth of a multitude of tumor cells in vitro and in vivo, thus constituting interesting leads for developing novel antitumor therapies. Furthermore, some other classes of compounds that interact with CAs have recently been discovered, some of which possess modified sulfonamide or hydroxamate moieties. Some sulfonamides have also applications as diagnostic tools, in PET and MRI or as antiepileptics or for the treatment of other neurological disorders. Future prospects for drug design applications for inhibitors of these ubiquitous enzymes are also discussed.

Multiple Binding Modes of Inhibitors to Carbonic Anhydrases: How to Design Specific Drugs Targeting 15 Different Isoforms?
Vincenzo Alterio, Anna Di Fiore, Katia D’Ambrosio et al.|Chemical Reviews|2012
Cited by 1.2kOpen Access

Carbonic anhydrases (CAs, EC 4.2.1.1) are ubiquitous metalloenzymes,
\npresent throughout most living organisms and
\nencoded by five evolutionarily unrelated gene families: the α-,
\nβ-, γ-, δ-, and ζ-CAs The α- β- and δ-CAs contain a Zn(II)
\nion at the active site, the γ-CAs are probably Fe(II) enzymes
\n(but they are active also with Zn(II) or Co(II) ions), while the
\nmetal ion is usually replaced by cadmium in the ζ-CAs. Herein we report a state of the art structural crystallographyc investigation.