ALZHEIMER DISEASE;
ARTICLE;
CONTROLLED STUDY;
DRUG ACTIVITY;
DRUG DESIGN;
DRUG SCREENING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
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Synthesis, acetylcholinesterase inhibition and neuroprotective activity of new tacrine analogues
Leon, R.; Marco-Contelles, J.; Garcia, A. G.; Villarroya, M. Synthesis, acetylcholinesterase inhibition and neuroprotective activity of new tacrine analogues. Bioorg. Med. Chem., 2005, 13, 1167-1175.
Design and synthesis of N-benzylpiperidine-purine derivatives as new dual inhibitors of acetyl- And butyrylcholinesterase
DOI 10.1016/j.bmc.2005.07.019, PII S0968089605006814
Rodriguez-Franco, M. I.; Fernandez-Bachiller, M. I.; Perez, C.; Castro, A.; Martinez, A. Design and synthesis of Nbenzylpiperidine-purine derivatives as new dual inhibitors of acetyl- and butyrylcholinesterase. Bioorg. Med. Chem., 2005, 13, 6795-6802. (Pubitemid 41571225)
Synthesis and nerve cell protection activities of tetrahydroacridine derivatives
Zhang, H. B.; Zhou, J. P.; Huang, W. L. Synthesis and nerve cell protection activities of tetrahydroacridine derivatives. J. Chin. Pharma. Univ., 2000, 31(6), 403-407.
Synthesis and biological activities of tetrahydroacridine derivatives
Zhou, J. P.; Zhang, H. B.; Huang, W. L. Synthesis and biological activities of tetrahydroacridine derivatives. Chin. J. Med. Chem., 2000, 10(3), 172-176.
A tetrahydroacridine derivative inhibits cerebral ischemia and protects rat cortical neurons against glutamateinduced cytotoxicity
Sheng, R.; Liu, G. Q. A tetrahydroacridine derivative inhibits cerebral ischemia and protects rat cortical neurons against glutamateinduced cytotoxicity. Acta. Pharmacol. Sin., 2003, 24(5), 390-393.
A modified Niementowski reaction for the synthesis of 4-hydroxyquinoline and its realted compounds
Son, J.; Kim S.; Jiang, Y. A modified niementowski reaction for the synthesis of 4-hydroxyquinoline and its realted compounds. Heterocycles, 2001, 55(10), 1981-1986. (Pubitemid 33020464)
(2001)Heterocycles, vol.55, Issue.10, pp. 1981-1986
Donepezil-tacrine hybrid related derivatives as new dual binding site inhibitors of AChE
DOI 10.1016/j.bmc.2005.09.029, PII S0968089605008990
Alonso, D.; Dorronsoro, I.; Rubio, L.; Munoz, P.; Garcia-Palomero, E.; Del Monte, M.; Bidon-Chanal, A.; Orozco, M.; Luque, F. J.; Castro, A.; Medina, M.; Martinez, A. Donepezil-tacrine hybrid related derivatives as new dual binding site inhibitors of AChE. Bioorg. Med. Chem., 2005, 13, 6588-6597. (Pubitemid 41571203)
Fused carbon rings. XIX. Experiments on the synthesis of tetracyclic compounds of the sexual hormone type
Burnop, V.; Elliott, G.; Linstead, R. Fused carbon rings. XIX. Experiments on the synthesis of tetracyclic compounds of the sexual hormone type. J. Chem. Soc., 1940, 727-735.
A new and rapid colorimetric determination of acetylcholinesterase activity
Ellman, G. L.; Courtney, K. D.; Andres, V.; Featherstone, R. M. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem. Pharmacol., 1961, 7 , 88-95.
Protective effects of 9-(4-ethoxycarboxylyphenoxy)-6,7-dimethoxy- 1,2,3, 4-tetrahydroacridine on anoxia and ischemic injury in cultured PC12 cells
Sheng, R.; Liu, G. Q. Protective effects of 9-(4-ethoxycarboxylyphenoxy)- 6,7-dimethoxy- 1,2,3, 4-tetrahydroacridine on anoxia and ischemic injury in cultured PC12 cells. Chin. J. Clin. Pharmacol. Ther., 2001, 6(4), 330-333.