Recent advances in indazole-containing derivatives: synthesis and biological perspectives

SG Zhang, CG Liang, WH Zhang - Molecules, 2018 - mdpi.com
Indazole-containing derivatives represent one of the most important heterocycles in drug
molecules. Diversely substituted indazole derivatives bear a variety of functional groups and …

Multiple Binding Modes of Inhibitors to Human Carbonic Anhydrases: An Update on the Design of Isoform-Specific Modulators of Activity

K D'Ambrosio, A Di Fiore, V Alterio, E Langella… - Chemical …, 2024 - ACS Publications
Human carbonic anhydrases (hCAs) are widespread zinc enzymes that catalyze the
hydration of CO2 to bicarbonate and a proton. Currently, 15 isoforms have been identified, of …

Synthesis of coumarin-sulfonamide derivatives and determination of their cytotoxicity, carbonic anhydrase inhibitory and molecular docking studies

BZ Kurt, F Sonmez, D Ozturk, A Akdemir… - European Journal of …, 2019 - Elsevier
Carbonic anhydrases isoforms CA IX, and XII are known to be highly expressed in various
human tissues and malignancies. CA IX is a prominent target for especially colorectal …

Carbonic anhydrases: Versatile and useful biocatalysts in chemistry and biochemistry

A Angeli, F Carta, CT Supuran - Catalysts, 2020 - mdpi.com
Metalloenzymes such as the carbonic anhydrases (CAs, EC 4.2. 1.1) possess highly
specialized active sites that promote fast reaction rates and high substrate selectivity for the …

Develo** hybrid molecule therapeutics for diverse enzyme inhibitory action: Active role of coumarin-based structural leads in drug discovery

A Ibrar, SA Shehzadi, F Saeed, I Khan - Bioorganic & Medicinal Chemistry, 2018 - Elsevier
Hybrid drugs featuring two or more potentially bioactive pharmacophores have been
recognized as advanced and superior chemical entities to simultaneously modulate multiple …

pH regulators and their inhibitors in tumor microenvironment

S Liao, G Wu, Z **e, X Lei, X Yang, S Huang… - European journal of …, 2024 - Elsevier
As an important characteristic of tumor, acidic tumor microenvironment (TME) is closely
related to immune escape, invasion, migration and drug resistance of tumor. The acidity of …

Synthesis, biological activity and multiscale molecular modeling studies of bis-coumarins as selective carbonic anhydrase IX and XII inhibitors with effective …

BZ Kurt, A Dag, B Doğan, S Durdagi, A Angeli… - Bioorganic …, 2019 - Elsevier
A series of novel bis-coumarin derivatives containing triazole moiety as a linker between the
alkyl chains was synthesized and their inhibitory activity against the human carbonic …

Tail-approach-based design and synthesis of coumarin-monoterpenes as carbonic anhydrase inhibitors and anticancer agents

B Zengin Kurt, G Celebi, D Ozturk Civelek, A Angeli… - ACS …, 2023 - ACS Publications
In this study, sixty novel coumarin-monoterpene compounds were synthesized in two series
[thirty-two compounds (12–43) bearing a triazole ring in the first series, and twenty-eight …

Synthesis and biological evaluation of coumarin-1, 3, 4-oxadiazole hybrids as selective carbonic anhydrase IX and XII inhibitors

SG Narella, MG Shaik, A Mohammed, M Alvala… - Bioorganic …, 2019 - Elsevier
With an aim to develop novel heterocyclic hybrids as potent anticancer agents, we
synthesized a series of coumarin-1, 3, 4-oxadiazole hybrids (7a-t) and evaluated for their …

Discovery of new 6-ureido/amidocoumarins as highly potent and selective inhibitors for the tumour-relevant carbonic anhydrases IX and XII

AK El-Damasy, HJ Kim, A Nocentini… - Journal of Enzyme …, 2023 - Taylor & Francis
A series of 6-ureido/amidocoumarins (5a–p and 7a–c) has been designed and synthesised
to develop potent and isoform-selective carbonic anhydrase h CA XI and XII inhibitors. All …