A. Granese

发表

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, semipreparative HPLC separation, biological evaluation, and 3D-QSAR of hydrazothiazole derivatives as human monoamine oxidase B inhibitors.

T. Langer, S. Carradori, J. Kirchmair, 2010, Bioorganic & medicinal chemistry.

A environmentally friendly reversed-phase liquid chromatography method for phthalates determination in nail cosmetics

D. Tonelli, A. Granese, D. Orsi, 2006 .

Synthesis and inhibitory activity against human monoamine oxidase of N1-thiocarbamoyl-3,5-di(hetero)aryl-4,5-dihydro-(1H)-pyrazole derivatives.

S. Carradori, D. Secci, M. Yáñez, 2010, European journal of medicinal chemistry.

Synthesis, stereochemical identification, and selective inhibitory activity against human monoamine oxidase-B of 2-methylcyclohexylidene-(4-arylthiazol-2-yl)hydrazones.

S. Carradori, D. Secci, S. Alcaro, 2008, Journal of medicinal chemistry.

Selective inhibitory activity against MAO and molecular modeling studies of 2-thiazolylhydrazone derivatives.

D. Secci, S. Alcaro, F. Ortuso, 2007, Journal of medicinal chemistry.

Synthesis and in vitro activity of 2-thiazolylhydrazone derivatives compared with the activity of clotrimazole against clinical isolates of Candida spp.

S. Carradori, D. Secci, E. Maccioni, 2007, Bioorganic & medicinal chemistry letters.

Synthesis and evaluation of 4-acyl-2-thiazolylhydrazone derivatives for anti-Toxoplasma efficacy in vitro.

S. Carradori, D. Secci, L. Jones-Brando, 2009, Journal of 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.

Synthesis and Evaluation of Thymol-Based Synthetic Derivatives as Dual-Action Inhibitors against Different Strains of H. pylori and AGS Cell Line

S. Carradori, Cristina Campestre, G. Mincione, 2021, Molecules.

Synthesis and in vitro selective anti-Helicobacter pylori activity of N-substituted-2-oxo-2H-1-benzopyran-3-carboxamides.

S. Carradori, D. Secci, A. Granese, 2006, European journal of medicinal chemistry.

Synthesis and Molecular Modelling of Novel Substituted‐4,5‐dihydro‐(1H)‐pyrazole Derivatives as Potent and Highly Selective Monoamine Oxidase‐A Inhibitors

D. Secci, S. Alcaro, F. Ortuso, 2006, Chemical biology & drug design.

Synthesis and anti-Helicobacter pylori Activity of 4-(Coumarin-3-yl)thiazol-2-ylhydrazone Derivatives.

S. Carradori, D. Secci, F. Sisto, 2011 .

Synthesis and anti-Helicobacter pylori activity of 4-(coumarin-3-yl)thiazol-2-ylhydrazone derivatives

S. Carradori, D. Secci, F. Sisto, 2010 .

Synthesis and biological evaluation of novel conjugated coumarin‐thiazole systems

S. Carradori, D. Secci, A. Granese, 2009 .

Synthesis, selective anti-Helicobacter pylori activity, and cytotoxicity of novel N-substituted-2-oxo-2H-1-benzopyran-3-carboxamides.

S. Carradori, D. Secci, A. Zicari, 2010, Bioorganic & medicinal chemistry letters.

A novel class of selective anti-Helicobacter pylori agents 2-oxo-2H-chromene-3-carboxamide derivatives.

S. Carradori, D. Secci, A. Zicari, 2007, Bioorganic & medicinal chemistry letters.

Synthesis and in vitro selective anti-Helicobacter pylori activity of pyrazoline derivatives.

D. Secci, A. Granese, F. Manna, 2005, Bioorganic & medicinal chemistry letters.

Investigations on the 2-thiazolylhydrazyne scaffold: synthesis and molecular modeling of selective human monoamine oxidase inhibitors.

S. Carradori, D. Secci, S. Alcaro, 2010, Bioorganic & medicinal chemistry.

Synthesis, molecular modeling, and selective inhibitory activity against human monoamine oxidases of 3-carboxamido-7-substituted coumarins.

Stefano Alcaro, Francesco Ortuso, Adriana Bolasco, 2009, Journal of medicinal chemistry.

LC Determination of Coumarin-3-Acyl Derivatives for Evaluation of the Stability and Monoamine Oxidase Inhibition Mechanism

D. Secci, A. Granese, D. Orsi, 2005 .

Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)- pyrazole derivatives.

D. Secci, S. Alcaro, R. Cirilli, 2005, Journal of medicinal chemistry.

Synthesis and biological evaluation of novel 2,4-disubstituted-1,3-thiazoles as anti-Candida spp. agents.

S. Carradori, D. Secci, A. Granese, 2011, European journal of medicinal chemistry.

A novel histone acetyltransferase inhibitor modulating Gcn5 network: cyclopentylidene-[4-(4'-chlorophenyl)thiazol-2-yl)hydrazone.

S. Carradori, P. Ballario, P. Filetici, 2009, 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.

Synthesis and inhibitory activity against human monoamine oxidase of N1-thiocarbamoyl-3,5-di(hetero)aryl-4,5-dihydro-(1H)-pyrazole derivatives.

S. Carradori, D. Secci, M. Yáñez, 2010, European journal of medicinal chemistry.

Inhibition of monoamine oxidases by coumarin-3-acyl derivatives: biological activity and computational study.

D. Secci, S. Alcaro, F. Ortuso, 2004, Bioorganic & medicinal chemistry letters.

Synthesis of New Diethynylbenzene Derivatives

D. Secci, A. Granese, F. Chimenti, 2004 .

Phytochemical analyses and pharmacological screening of Neem oil

G. Zengin, M. Locatelli, F. Cacciagrano, 2019, South African Journal of Botany.

Synthesis and characterization of new 3‐acyl‐7‐hydroxy‐6,8‐substituted‐coumarin and 3‐acyl‐7‐benzyloxy‐6,8‐substituted‐coumarin derivatives

S. Carradori, D. Secci, A. Granese, 2010 .

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.

Antimicrobial activity, synergism and inhibition of germ tube formation by Crocus sativus-derived compounds against Candida spp.

S. Carradori, L. Angiolella, A. Granese, 2016, Journal of enzyme inhibition and medicinal chemistry.

Synthesis and selective inhibition of human monoamine oxidases of a large scaffold of (4,5-substituted-thiazol-2-yl)hydrazones

S. Carradori, D. Secci, M. Yáñez, 2010 .

Synthesis, stereochemical separation, and biological evaluation of selective inhibitors of human MAO-B: 1-(4-arylthiazol-2-yl)-2-(3-methylcyclohexylidene)hydrazines.

S. Carradori, D. Secci, R. Cirilli, 2010, Journal of medicinal chemistry.

A Novel Class of Dual-Acting DCH-CORMs Counteracts Oxidative Stress-Induced Inflammation in Human Primary Tenocytes

S. Carradori, Cristina Campestre, M. Gallorini, 2021, Antioxidants.

Quercetin as the active principle of Hypericum hircinum exerts a selective inhibitory activity against MAO-A: extraction, biological analysis, and computational study.

Stefano Alcaro, Francesco Ortuso, Adriana Bolasco, 2006, Journal of natural products.

Synthesis, biological evaluation and 3D-QSAR of 1,3,5-trisubstituted-4,5-dihydro-(1H)-pyrazole derivatives as potent and highly selective monoamine oxidase A inhibitors.

T. Langer, D. Secci, S. Alcaro, 2006, Current Medicinal Chemistry.

Novel therapeutic opportunities for Toxoplasma gondii, Trichomonas vaginalis, and Giardia intestinalis infections

A. Granese, P. Chimenti, Paolo Guglielmi, 2023, Expert opinion on therapeutic patents.

Analysis of corticosteroids by high performance liquid chromatography-electrospray mass spectrometry.

D. Tonelli, E. Camera, M. Picardo, 2004, The Analyst.

Development of an HPLC method for the identification and dosage of non-allowed substances in cosmetic products. Part I: local anaesthetics and antihistaminics

D. Tonelli, A. Granese, D. Orsi, 2004, Analytical and bioanalytical chemistry.

Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of N,N'-bis[2-oxo-2H-benzopyran]-3-carboxamides.

S. Carradori, D. Secci, S. Alcaro, 2006, Bioorganic & medicinal chemistry letters.

Recent developments of agents targeting Vibrio cholerae: patents and literature data

Cristina Campestre, A. Granese, Francesco Melfi, 2024, Expert opinion on therapeutic patents.