Espinosa-Jimenez T, Cano A, Sanchez-Lopez E, Olloquequi J, Folch J, Bullo M, Verdaguer E, Auladell C, Pont C, Munoz-Torrero D, Parcerisas A, Camins A, Ettcheto M (2023)
A novel rhein-huprine hybrid ameliorates disease-modifying properties in preclinical mice model of Alzheimer's disease exacerbated with high fat diet
Cell Biosci 13: 52

Codony S, Pont C, Grinan-Ferre C, Di Pede-Mattatelli A, Calvo-Tusell C, Feixas F, Osuna S, Jarne-Ferrer J, Naldi M, Bartolini M, Loza MI, Brea J, Perez B, Bartra C, Sanfeliu C, Juarez-Jimenez J, Morisseau C, Hammock BD, Pallas M, Vazquez S, Munoz-Torrero D (2022)
Discovery and In Vivo Proof of Concept of a Highly Potent Dual Inhibitor of Soluble Epoxide Hydrolase and Acetylcholinesterase for the Treatment of Alzheimer's Disease
Journal of Medicinal Chemistry 65: 4909

Jarne-Ferrer J, Grinan-Ferre C, Bellver-Sanchis A, Vazquez S, Munoz-Torrero D, Pallas M (2022)
A Combined Chronic Low-Dose Soluble Epoxide Hydrolase and Acetylcholinesterase Pharmacological Inhibition Promotes Memory Reinstatement in Alzheimer's Disease Mice Models
Pharmaceuticals (Basel) 15:

Sampietro A, Perez-Areales FJ, Martinez P, Arce EM, Galdeano C, Munoz-Torrero D (2022)
Unveiling the Multitarget Anti-Alzheimer Drug Discovery Landscape: A Bibliometric Analysis
Pharmaceuticals (Basel) 15:

Pont C, Ginex T, Grinan-Ferre C, Scheiner M, Mattellone A, Martinez N, Arce EM, Soriano-Fernandez Y, Naldi M, De Simone A, Barenys M, Gomez-Catalan J, Perez B, Sabate R, Andrisano V, Loza MI, Brea J, Bartolini M, Bolognesi ML, Decker M, Pallas M, Luque FJ, Munoz-Torrero D (2021)
From virtual screening hits targeting a cryptic pocket in BACE-1 to a nontoxic brain permeable multitarget anti-Alzheimer lead with disease-modifying and cognition-enhancing effects
Eur Journal of Medicinal Chemistry 225: 113779

Viayna E, Coquelle N, Cieslikiewicz-Bouet M, Cisternas P, Oliva CA, Sanchez-Lopez E, Ettcheto M, Bartolini M, De Simone A, Ricchini M, Rendina M, Pons M, Firuzi O, Perez B, Saso L, Andrisano V, Nachon F, Brazzolotto X, Garcia ML, Camins A, Silman I, Jean L, Inestrosa NC, Colletier JP, Renard PY, Munoz-Torrero D (2021)
Discovery of a Potent Dual Inhibitor of Acetylcholinesterase and Butyrylcholinesterase with Antioxidant Activity that Alleviates Alzheimer-like Pathology in Old APP/PS1 Mice
Journal of Medicinal Chemistry 64: 812

Zambrano P, Suwalsky M, Jemiola-Rzeminska M, Gallardo-Nelson MJ, Strzalka K, Munoz-Torrero D (2021)
Protective Role of a Donepezil-Huprine Hybrid against the beta-Amyloid (1-42) Effect on Human Erythrocytes
Int J Mol Sci 22:

Perez-Areales FJ, Garrido M, Aso E, Bartolini M, De Simone A, Espargaro A, Ginex T, Sabate R, Perez B, Andrisano V, Puigoriol-Illamola D, Pallas M, Luque FJ, Loza MI, Brea J, Ferrer I, Ciruela F, Messeguer A, Munoz-Torrero D (2020)
Centrally Active Multitarget Anti-Alzheimer Agents Derived from the Antioxidant Lead CR-6
Journal of Medicinal Chemistry 63: 9360

Perez-Areales FJ, Turcu AL, Barniol-Xicota M, Pont C, Pivetta D, Espargaro A, Bartolini M, De Simone A, Andrisano V, Perez B, Sabate R, Sureda FX, Vazquez S, Munoz-Torrero D (2019)
A novel class of multitarget anti-Alzheimer benzohomoadamantanechlorotacrine hybrids modulating cholinesterases and glutamate NMDA receptors
Eur Journal of Medicinal Chemistry 180: 613

Galdeano C, Coquelle N, Cieslikiewicz-Bouet M, Bartolini M, Perez B, Clos MV, Silman I, Jean L, Colletier JP, Renard PY, Munoz-Torrero D (2018)
Increasing Polarity in Tacrine and Huprine Derivatives: Potent Anticholinesterase Agents for the Treatment of Myasthenia Gravis
Molecules 23:

Relat J, Perez B, Camps P, Munoz-Torrero D, Badia A, Victoria Clos M (2018)
Huprine X Attenuates The Neurotoxicity Induced by Kainic Acid, Especially Brain Inflammation
Basic Clin Pharmacol Toxicol 122: 94

Relat J, Come J, Perez B, Camps P, Munoz-Torrero D, Badia A, Gimenez-Llort L, Clos MV (2018)
Neuroprotective Effects of the Multitarget Agent AVCRI104P3 in Brain of Middle-Aged Mice
Int J Mol Sci 19:

Gimenez-Llort L, Ratia M, Perez B, Camps P, Munoz-Torrero D, Badia A, Clos MV (2017)
Behavioural effects of novel multitarget anticholinesterasic derivatives in Alzheimer's disease
Behav Pharmacol 28: 124

Perez-Areales FJ, Betari N, Viayna A, Pont C, Espargaro A, Bartolini M, De Simone A, Rinaldi Alvarenga JF, Perez B, Sabate R, Lamuela-Raventos RM, Andrisano V, Luque FJ, Munoz-Torrero D (2017)
Design, synthesis and multitarget biological profiling of second-generation anti-Alzheimer rhein-huprine hybrids
Future Med Chem 9: 965

Decker M, Munoz-Torrero D (2016)
Special Issue: Molecules against Alzheimer
Molecules 21:

Serrano FG, Tapia-Rojas C, Carvajal FJ, Cisternas P, Viayna E, Sola I, Munoz-Torrero D, Inestrosa NC (2016)
Rhein-Huprine Derivatives Reduce Cognitive Impairment, Synaptic Failure and Amyloid Pathology in AbetaPPswe/PS-1 Mice of Different Ages
Curr Alzheimer Res 13: 1017

Di Pietro O, Vicente-Garcia E, Taylor MC, Berenguer D, Viayna E, Lanzoni A, Sola I, Sayago H, Riera C, Fisa R, Clos MV, Perez B, Kelly JM, Lavilla R, Munoz-Torrero D (2015)
Multicomponent reaction-based synthesis and biological evaluation of tricyclic heterofused quinolines with multi-trypanosomatid activity
Eur Journal of Medicinal Chemistry 105: 120

Gimenez-Llort L, Ratia M, Perez B, Camps P, Munoz-Torrero D, Badia A, Clos MV (2015)
AVCRI104P3, a novel multitarget compound with cognition-enhancing and anxiolytic activities: Studies in cognitively poor middle-aged mice
Behavioural Brain Research 286: 97

Sola I, Aso E, Frattini D, Lopez-Gonzalez I, Espargaro A, Sabate R, Di Pietro O, Luque FJ, Clos MV, Ferrer I, Munoz-Torrero D (2015)
Novel Levetiracetam Derivatives That Are Effective against the Alzheimer-like Phenotype in Mice: Synthesis, in Vitro, ex Vivo, and in Vivo Efficacy Studies
Journal of Medicinal Chemistry 58: 6018

Sola I, Castella S, Viayna E, Galdeano C, Taylor MC, Gbedema SY, Perez B, Clos MV, Jones DC, Fairlamb AH, Wright CW, Kelly JM, Munoz-Torrero D (2015)
Synthesis, biological profiling and mechanistic studies of 4-aminoquinoline-based heterodimeric compounds with dual trypanocidal-antiplasmodial activity
Bioorganic & Medicinal Chemistry 23: 5156

Torrent J, Vilchez-Acosta A, Munoz-Torrero D, Trovaslet M, Nachon F, Chatonnet A, Grznarova K, Acquatella-Tran Van Ba I, Le Goffic R, Herzog L, Beringue V, Rezaei H (2015)
Interaction of prion protein with acetylcholinesterase: potential pathobiological implications in prion diseases
Acta Neuropathologica Commun 3: 18

Di Pietro O, Perez-Areales FJ, Juarez-Jimenez J, Espargaro A, Clos MV, Perez B, Lavilla R, Sabate R, Luque FJ, Munoz-Torrero D (2014)
Tetrahydrobenzo[h][1,6]naphthyridine-6-chlorotacrine hybrids as a new family of anti-Alzheimer agents targeting beta-amyloid, tau, and cholinesterase pathologies
Eur Journal of Medicinal Chemistry 84C: 107

Perez-Areales FJ, Di Pietro O, Espargaro A, Vallverdu-Queralt A, Galdeano C, Ragusa IM, Viayna E, Guillou C, Clos MV, Perez B, Sabate R, Lamuela-Raventos RM, Luque FJ, Munoz-Torrero D (2014)
Shogaol-huprine hybrids: Dual antioxidant and anticholinesterase agents with beta-amyloid and tau anti-aggregating properties
Bioorganic & Medicinal Chemistry 22: 5298

Sola I, Artigas A, Taylor MC, Gbedema SY, Perez B, Clos MV, Wright CW, Kelly JM, Munoz-Torrero D (2014)
Synthesis and antiprotozoal activity of oligomethylene- and p-phenylene-bis(methylene)-linked bis(+)-huprines
Bioorganic & Medicinal Chemistry Lett 24: 5435

Viayna E, Sola I, Bartolini M, De Simone A, Tapia-Rojas C, Serrano FG, Sabate R, Juarez-Jimenez J, Perez B, Luque FJ, Andrisano V, Clos MV, Inestrosa NC, Munoz-Torrero D (2014)
Synthesis and multitarget biological profiling of a novel family of rhein derivatives as disease-modifying anti-Alzheimer agents
Journal of Medicinal Chemistry 57: 2549

Di Pietro O, Viayna E, Vicente-Garcia E, Bartolini M, Ramon R, Juarez-Jimenez J, Clos MV, Perez B, Andrisano V, Luque FJ, Lavilla R, Munoz-Torrero D (2013)
1,2,3,4-Tetrahydrobenzo[h][1,6]naphthyridines as a new family of potent peripheral-to-midgorge-site inhibitors of acetylcholinesterase: Synthesis, pharmacological evaluation and mechanistic studies
Eur Journal of Medicinal Chemistry 73C: 141

Pera M, Camps P, Munoz-Torrero D, Perez B, Badia A, Clos Guillen MV (2013)
Undifferentiated and Differentiated PC12 Cells Protected by Huprines Against Injury Induced by Hydrogen Peroxide
PLoS ONE 8: e74344

Ratia M, Gimenez-Llort L, Camps P, Munoz-Torrero D, Perez B, Clos MV, Badia A (2013)
Huprine X and Huperzine A Improve Cognition and Regulate Some Neurochemical Processes Related with Alzheimer's Disease in Triple Transgenic Mice (3xTg-AD)
Neurodegener Dis 11: 129

Galdeano C, Viayna E, Sola I, Formosa X, Camps P, Badia A, Clos MV, Relat J, Ratia M, Bartolini M, Mancini F, Andrisano V, Salmona M, Minguillon C, Gonzalez-Munoz GC, Rodriguez-Franco MI, Bidon-Chanal A, Luque FJ, Munoz-Torrero D (2012)
Huprine-tacrine heterodimers as anti-amyloidogenic compounds of potential interest against Alzheimer's and prion diseases
Journal of Medicinal Chemistry 55: 661

Munoz-Torrero D, Pera M, Relat J, Ratia M, Galdeano C, Viayna E, Sola I, Formosa X, Camps P, Badia A, Clos MV (2012)
Expanding the multipotent profile of huprine-tacrine heterodimers as disease-modifying anti-Alzheimer agents
Neurodegener Dis 10: 96

Defaux J, Sala M, Formosa X, Galdeano C, Taylor MC, Alobaid WA, Kelly JM, Wright CW, Camps P, Munoz-Torrero D (2011)
Huprines as a new family of dual acting trypanocidal-antiplasmodial agents
Bioorganic & Medicinal Chemistry 19: 1702

Camps P, Formosa X, Galdeano C, Gomez T, Munoz-Torrero D, Ramirez L, Viayna E, Gomez E, Isambert N, Lavilla R, Badia A, Clos MV, Bartolini M, Mancini F, Andrisano V, Bidon-Chanal A, Huertas O, Dafni T, Luque FJ (2010)
Tacrine-based dual binding site acetylcholinesterase inhibitors as potential disease-modifying anti-Alzheimer drug candidates
Chemico-Biological Interactions 187: 411

Galdeano C, Viayna E, Arroyo P, Bidon-Chanal A, Blas JR, Munoz-Torrero D, Luque FJ (2010)
Structural determinants of the multifunctional profile of dual binding site acetylcholinesterase inhibitors as anti-Alzheimer agents
Curr Pharm Des 16: 2818

Hedberg MM, Clos MV, Ratia M, Gonzalez D, Lithner CU, Camps P, Munoz-Torrero D, Badia A, Gimenez-Llort L, Nordberg A (2010)
Effect of huprine X on beta-amyloid, synaptophysin and alpha7 neuronal nicotinic acetylcholine receptors in the brain of 3xTg-AD and APPswe transgenic mice
Neurodegener Dis 7: 379

Viayna E, Gomez T, Galdeano C, Ramirez L, Ratia M, Badia A, Clos MV, Verdaguer E, Junyent F, Camins A, Pallas M, Bartolini M, Mancini F, Andrisano V, Arce MP, Rodriguez-Franco MI, Bidon-Chanal A, Luque FJ, Camps P, Munoz-Torrero D (2010)
Novel huprine derivatives with inhibitory activity toward beta-amyloid aggregation and formation as disease-modifying anti-Alzheimer drug candidates
ChemMedChem 5: 1855

Camps P, Formosa X, Galdeano C, Munoz-Torrero D, Ramirez L, Gomez E, Isambert N, Lavilla R, Badia A, Clos MV, Bartolini M, Mancini F, Andrisano V, Arce MP, Rodriguez-Franco MI, Huertas O, Dafni T, Luque FJ (2009)
Pyrano[3,2-c]quinoline-6-chlorotacrine hybrids as a novel family of acetylcholinesterase- and beta-amyloid-directed anti-Alzheimer compounds
Journal of Medicinal Chemistry 52: 5365

Camps P, Formosa X, Galdeano C, Gomez T, Munoz-Torrero D, Scarpellini M, Viayna E, Badia A, Clos MV, Camins A, Pallas M, Bartolini M, Mancini F, Andrisano V, Estelrich J, Lizondo M, Bidon-Chanal A, Luque FJ (2008)
Novel donepezil-based inhibitors of acetyl- and butyrylcholinesterase and acetylcholinesterase-induced beta-amyloid aggregation
Journal of Medicinal Chemistry 51: 3588

Munoz-Torrero D (2008)
Acetylcholinesterase inhibitors as disease-modifying therapies for Alzheimer's disease
Curr Med Chem 15: 2433

Camps P, Gomez E, Munoz-Torrero D, Badia A, Clos MV, Curutchet C, Munoz-Muriedas J, Luque FJ (2006)
Binding of 13-amidohuprines to acetylcholinesterase: exploring the ligand-induced conformational change of the gly117-gly118 peptide bond in the oxyanion hole
Journal of Medicinal Chemistry 49: 6833

Clos MV, Pera M, Ratia M, Roman S, Camps P, Munoz-Torrero D, Colombo L, Salmona M, Badia A (2006)
Effect of acetylcholinesterase inhibitors on AChE-induced PrP106-126 aggregation
Journal of Molecular Neuroscience 30: 89

Munoz-Torrero D, Camps P (2006)
Dimeric and hybrid anti-Alzheimer drug candidates
Curr Med Chem 13: 399

Pera M, Roman S, Ratia M, Camps P, Munoz-Torrero D, Colombo L, Manzoni C, Salmona M, Badia A, Clos MV (2006)
Acetylcholinesterase triggers the aggregation of PrP 106-126
Biochemical & Biophysical Research Communications 346: 89

Camps P, Formosa X, Munoz-Torrero D, Petrignet J, Badia A, Clos MV (2005)
Synthesis and pharmacological evaluation of huprine-tacrine heterodimers: subnanomolar dual binding site acetylcholinesterase inhibitors
Journal of Medicinal Chemistry 48: 1701

Roman S, Badia A, Camps P, Munoz-Torrero D, Clos MV (2005)
Nicotinic-receptor potentiator drugs, huprine X and galantamine, increase ACh release by blocking AChE activity but not acting on nicotinic receptors
Brain Research 1061: 73

Jorda EG, Verdaguer E, Jimenez A, Canudas AM, Rimbau V, Camps P, Munoz-Torrero D, Camins A, Pallas M (2004)
(+/-)-huprine Y, (-)-huperzine A and tacrine do not show neuroprotective properties in an apoptotic model of neuronal cytoskeletal alteration
J Alzheimers Dis 6: 577

Alcala Mdel M, Vivas NM, Hospital S, Camps P, Munoz-Torrero D, Badia A (2003)
Characterisation of the anticholinesterase activity of two new tacrine-huperzine A hybrids
Neuropharmacology 44: 749

Camps P, Munoz-Torrero D (2002)
Cholinergic drugs in pharmacotherapy of Alzheimer's disease
Mini Rev Med Chem 2: 11

Dvir H, Wong DM, Harel M, Barril X, Orozco M, Luque FJ, Munoz-Torrero D, Camps P, Rosenberry TL, Silman I, Sussman JL (2002)
3D structure of Torpedo californica acetylcholinesterase complexed with huprine X at 2.1 A resolution: kinetic and molecular dynamic correlates
Biochemistry 41: 2970

Camps P, Gomez E, Munoz-Torrero D, Badia A, Vivas NM, Barril X, Orozco M, Luque FJ (2001)
Synthesis, in Vitro Pharmacology, and Molecular Modeling of syn-Huprines as Acetylcholinesterase Inhibitors
Journal of Medicinal Chemistry 44: 4733

Camps P, Munoz-Torrero D (2001)
Tacrine-huperzine A hybrids (huprines): a new class of highly potent and selective acetylcholinesterase inhibitors of interest for the treatment of Alzheimer's disease
Mini Rev Med Chem 1: 163

Ros E, Aleu J, Gomez de Aranda I, Munoz-Torrero D, Camps P, Badia A, Marsal J, Solsona C (2001)
The pharmacology of novel acetylcholinesterase inhibitors, (+/-)- huprines Y and X, on the Torpedo electric organ
European Journal of Pharmacology 421: 77

Camps P, Cusack B, Mallender WD, Achab RE, Morral J, Munoz-Torrero D, Rosenberry TL (2000)
Huprine X is a Novel High-Affinity Inhibitor of Acetylcholinesterase That Is of Interest for Treatment of Alzheimer's Disease
Molecular Pharmacology 57: 409

Camps P, El Achab R, Morral J, Munoz-Torrero D, Badia A, Banos JE, Vivas NM, Barril X, Orozco M, Luque FJ (2000)
New tacrine-huperzine A hybrids (huprines): highly potent tight-binding acetylcholinesterase inhibitors of interest for the treatment of Alzheimer's disease
Journal of Medicinal Chemistry 43: 4657

Camps P, El Achab R, Gorbig DM, Morral J, Munoz-Torrero D, Badia A, Eladi Banos J, Vivas NM, Barril X, Orozco M, Luque FJ (1999)
Synthesis, in vitro pharmacology, and molecular modeling of very potent tacrine-huperzine A hybrids as acetylcholinesterase inhibitors of potential interest for the treatment of Alzheimer's disease
Journal of Medicinal Chemistry 42: 3227

Badia A, Banos JE, Camps P, Contreras J, Gorbig DM, Munoz-Torrero D, Simon M, Vivas NM (1998)
Synthesis and evaluation of tacrine-huperzine A hybrids as acetylcholinesterase inhibitors of potential interest for the treatment of Alzheimer's disease
Bioorganic & Medicinal Chemistry 6: 427