C. De Monte

发表

Dual Cyclooxygenase and Carbonic Anhydrase Inhibition by Nonsteroidal Anti-Inflammatory Drugs for the Treatment of Cancer.

C. De Monte, S. Carradori, A. Gentili, 2015, Current medicinal chemistry.

Modern extraction techniques and their impact on the pharmacological profile of Serenoa repens extracts for the treatment of lower urinary tract symptoms

C. De Monte, S. Carradori, C. De Nunzio, 2014, BMC Urology.

Synthesis and Selective Inhibitory Activity Against Human COX‐1 of Novel 1‐(4‐Substituted‐thiazol‐2‐yl)‐3,5‐di(hetero)aryl‐pyrazoline Derivatives

C. De Monte, S. Carradori, D. Secci, 2012, Archiv der Pharmazie.

Novel 1,3-thiazolidin-4-one derivatives as promising anti-Candida agents endowed with anti-oxidant and chelating properties.

C. De Monte, S. Carradori, A. Mollica, 2016, European journal of medicinal chemistry.

Design, synthesis and biological activity of selective hCAs inhibitors based on 2-(benzylsulfinyl)benzoic acid scaffold

C. De Monte, S. Carradori, C. Supuran, 2019, Journal of enzyme inhibition and medicinal chemistry.

Nitric Oxide Donors and Selective Carbonic Anhydrase Inhibitors: A Dual Pharmacological Approach for the Treatment of Glaucoma, Cancer and Osteoporosis

C. De Monte, S. Carradori, A. Mollica, 2015, Molecules.

Design, synthesis and biochemical evaluation of novel multi-target inhibitors as potential anti-Parkinson agents.

C. De Monte, S. Carradori, G. Zengin, 2018, European journal of medicinal chemistry.

Salen and tetrahydrosalen derivatives act as effective inhibitors of the tumor-associated carbonic anhydrase XII--a new scaffold for designing isoform-selective inhibitors.

C. De Monte, S. Carradori, C. Supuran, 2013, Bioorganic & medicinal chemistry letters.

Design, synthesis and biological characterization of thiazolidin-4-one derivatives as promising inhibitors of Toxoplasma gondii.

C. De Monte, S. Carradori, D. Secci, 2014, European journal of medicinal chemistry.

Synthesis, biological evaluation and quantitative structure-active relationships of 1,3-thiazolidin-4-one derivatives. A promising chemical scaffold endowed with high antifungal potency and low cytotoxicity.

C. De Monte, S. Carradori, R. Grande, 2017, European journal of medicinal chemistry.

(Thiazol-2-yl)hydrazone derivatives from acetylpyridines as dual inhibitors of MAO and AChE: synthesis, biological evaluation and molecular modeling studies

C. De Monte, S. Carradori, R. Di Santo, 2015, Journal of enzyme inhibition and medicinal chemistry.

Anti-Candida activity and cytotoxicity of a large library of new N-substituted-1,3-thiazolidin-4-one derivatives.

C. De Monte, S. Carradori, A. Mollica, 2016, European journal of medicinal chemistry.

Evaluation of a large library of (thiazol-2-yl)hydrazones and analogues as histone acetyltransferase inhibitors: enzyme and cellular studies.

C. De Monte, S. Carradori, L. Altucci, 2014, European journal of medicinal chemistry.

Synthesis and biological evaluation of anti-Toxoplasma gondii activity of a novel scaffold of thiazolidinone derivatives

C. De Monte, S. Carradori, Cristina Campestre, 2017, Journal of enzyme inhibition and medicinal chemistry.

Bioactive compounds of Crocus sativus L. and their semi-synthetic derivatives as promising anti-Helicobacter pylori, anti-malarial and anti-leishmanial agents

S. Parapini, C. De Monte, S. Carradori, 2015, Journal of enzyme inhibition and medicinal chemistry.

Identification of the stereochemical requirements in the 4-aryl-2-cycloalkylidenhydrazinylthiazole scaffold for the design of selective human monoamine oxidase B inhibitors.

C. De Monte, S. Carradori, L. Mannina, 2014, Bioorganic & medicinal chemistry.

A novel library of saccharin and acesulfame derivatives as potent and selective inhibitors of carbonic anhydrase IX and XII isoforms.

C. De Monte, S. Carradori, A. Mollica, 2016, Bioorganic & medicinal chemistry.

Synthesis and Selective Human Monoamine Oxidase B Inhibition of Heterocyclic Hybrids Based on Hydrazine and Thiazole Scaffolds

C. De Monte, S. Carradori, D. Secci, 2013, Archiv der Pharmazie.

Design, synthesis and evaluation of N-substituted saccharin derivatives as selective inhibitors of tumor-associated carbonic anhydrase XII.

C. De Monte, S. Carradori, C. Supuran, 2014, Bioorganic & medicinal chemistry.

Computational investigation of the selectivity of salen and tetrahydrosalen compounds towards the tumor-associated hCA XII isozyme

C. De Monte, S. Carradori, C. Supuran, 2015, Journal of enzyme inhibition and medicinal chemistry.

New amide derivatives of Probenecid as selective inhibitors of carbonic anhydrase IX and XII: biological evaluation and molecular modelling studies.

C. De Monte, S. Carradori, A. Mollica, 2015, Bioorganic & medicinal chemistry.

Bladder cancer: innovative approaches beyond the diagnosis.

C. De Monte, S. Carradori, R. Piergentili, 2014, Current medicinal chemistry.

New insights into the biological properties of Crocus sativus L.: chemical modifications, human monoamine oxidases inhibition and molecular modeling studies.

C. De Monte, S. Carradori, L. Mannina, 2014, European journal of medicinal chemistry.

Geographical characterization by MAE-HPLC and NIR methodologies and carbonic anhydrase inhibition of Saffron components.

C. De Monte, S. Carradori, A. Mollica, 2017, Food chemistry.

Synthesis and pharmacological screening of a large library of 1,3,4-thiadiazolines as innovative therapeutic tools for the treatment of prostate cancer and melanoma.

C. De Monte, S. Carradori, A. Mollica, 2015, European journal of medicinal chemistry.

Cyclic tertiary sulfamates: selective inhibition of the tumor-associated carbonic anhydrases IX and XII by N- and O-substituted acesulfame derivatives.

C. De Monte, S. Carradori, C. Supuran, 2014, European journal of medicinal chemistry.