AAAAAA

   
Results: 1-8 |
Results: 8
Easy access to 4-substituted (+/-)-huperzine A analogues
Authors: Camps, P Munoz-Torrero, D Simon, M
Citation: P. Camps et al., Easy access to 4-substituted (+/-)-huperzine A analogues, SYN COMMUN, 31(22), 2001, pp. 3507-3516
The pharmacology of novel acetylcholinesterase inhibitors, (+/-)-huprines Y and X, on the Torpedo electric organ
Authors: Ros, E Aleu, J de Aranda, IG Munoz-Torrero, D Camps, P Badia, A Marsal, J Solsona, C
Citation: E. Ros et al., The pharmacology of novel acetylcholinesterase inhibitors, (+/-)-huprines Y and X, on the Torpedo electric organ, EUR J PHARM, 421(2), 2001, pp. 77-84
Synthesis of polysubstituted bicyclo[3.3.1]nonane-3,7-diones from cyclohexa-2,5-dienones and dimethyl 1,3-acetonedicarboxylate
Authors: Camps, P Gonzalez, A Munoz-Torrero, D Simon, M Zuniga, A Martins, MA Font-Bardia, M Solans, X
Citation: P. Camps et al., Synthesis of polysubstituted bicyclo[3.3.1]nonane-3,7-diones from cyclohexa-2,5-dienones and dimethyl 1,3-acetonedicarboxylate, TETRAHEDRON, 56(41), 2000, pp. 8141-8151
New syntheses of rac-huperzine A and its rac-7-ethyl-derivative. Evaluation of several huperzine A analogues as acetylcholinesterase inhibitors
Authors: Camps, P Contreras, J El Achab, R Morral, J Munoz-Torrero, D Font-Bardia, M Solans, X Badia, A Vivas, NM
Citation: P. Camps et al., New syntheses of rac-huperzine A and its rac-7-ethyl-derivative. Evaluation of several huperzine A analogues as acetylcholinesterase inhibitors, TETRAHEDRON, 56(26), 2000, pp. 4541-4553
Huprine X is a novel high-affinity inhibitor of acetylcholinesterase that is of interest for treatment of Alzheimer's disease
Authors: Camps, P Cusack, B Mallender, WD El Achab, R Morral, J Munoz-Torrero, D Rosenberry, TL
Citation: P. Camps et al., Huprine X is a novel high-affinity inhibitor of acetylcholinesterase that is of interest for treatment of Alzheimer's disease, MOLEC PHARM, 57(2), 2000, pp. 409-417
New tacrine-huperzine A hybrids (huprines): Highly potent tight-binding acetylcholinesterase inhibitors of interest for the treatment of Alzheimer's disease
Authors: Camps, P El Achab, R Morral, J Munoz-Torrero, D Badia, A Banos, JE Vivas, NM Barril, X Orozco, M Luque, FJ
Citation: P. Camps et al., New tacrine-huperzine A hybrids (huprines): Highly potent tight-binding acetylcholinesterase inhibitors of interest for the treatment of Alzheimer's disease, J MED CHEM, 43(24), 2000, pp. 4657-4666
Synthesis of an 11-unsubstituted analogue of (+/-)-huperzine A
Authors: Camps, P Contreras, J Morral, J Munoz-Torrero, D Font-Bardia, M Solans, X
Citation: P. Camps et al., Synthesis of an 11-unsubstituted analogue of (+/-)-huperzine A, TETRAHEDRON, 55(28), 1999, pp. 8481-8496
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
Authors: Camps, P El Achab, R Gorbig, DM Morral, J Munoz-Torrero, D Badia, A Banos, JE Vivas, NM Barril, X Orozco, M Luque, FJ
Citation: P. Camps et al., 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, J MED CHEM, 42(17), 1999, pp. 3227-3242
Risultati: 1-8 |