ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CATALYST;
CRYSTAL STRUCTURE;
DRUG STRUCTURE;
DRUG SYNTHESIS;
INFRARED RADIATION;
MASS SPECTROMETRY;
POLYMERIZATION;
PROTON NUCLEAR MAGNETIC RESONANCE;
STRUCTURE ANALYSIS;
SUBSTITUTION REACTION;
X RAY DIFFRACTION;
Synthesis of acridine-nuclear localization signal (NLS) conjugates and evaluation of their impact on lipoplex and polyplex-based transfection
Boulanger, C.; Giorgio, C.; Vierling, P. Synthesis of acridine-nuclear localization signal (NLS) conjugates and evaluation of their impact on lipoplex and polyplex-based transfection. Eur. J. Med. Chem. 2005, 40 (12), 1295.
Trisubstituted acridines as G-quadruplex telomere targeting agents: Effects of extensions of the 3, 6- and 9-side chains on quadruplex binding, telomerase activity, and cell proliferation
Moor, M. J.; Schultes, C. M.; Cuesta, J.; Cuenca, F.; Gunaratnam, M.; Tanious, F. A. Trisubstituted acridines as G-quadruplex telomere targeting agents: Effects of extensions of the 3, 6- and 9-side chains on quadruplex binding, telomerase activity, and cell proliferation. J. Med. Chem. 2006, 49(2), 582.
Reactivity of the acridine ring: One-pot regioselective single and double bromomethylation of acridine and some derivatives
Chiron, J.; Galy, J. P. Reactivity of the acridine ring: One-pot regioselective single and double bromomethylation of acridine and some derivatives. Synthesis2004, 3, 313.
An efficient one-pot synthesis of N-carboxymethylacridine-1,8- dione derivatives under microwave irradiation
Tu, S. J.; Wang, Q.; Zhang, Y.; Xu, J. N.; Zhang, J. P.; Zhu, X. T.; Shi, F. J. An efficient one-pot synthesis of N-carboxymethylacridine-1,8- dione derivatives under microwave irradiation. Hererocycl. Chem. 2006, 43 (6), 1647.
Shutske, G. M.; Pierrat, F. A.; Kapples, K. J.; Cornfeldt, M. L.; Szewczak, M. R.; Huger, F. P.; Bores, G. M.; Haroutunian, V.; Davis, K. L. 9-Amino-1,2,3,4-tetrahydroacridin-1-ols: Synthesis and evaluation as potential Alzheimer's disease therapeutics. J. Med. Chem. 1989, 32, 1805.
Shutske, G. M.; Pierrat, F. A.; Kapples, K. J.; Cornfeldt, M. L.; Szewczak, M. R.; Huger, F. P.; Bores, G. M.; Haroutunian, V.; Davis, K. L. 9-Amino-1,2,3,4-tetrahydroacridin-1-ols: Synthesis and evaluation as potential Alzheimer's disease therapeutics. J. Med. Chem. 1989, 32, 1805.
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Prazosin-related compounds: Effect of transforming the piperazinylquinazoline moiety into an aminomethyltetrahydroacridine system on the affinity for a1-adrenoreceptors
Rosini, M.; Antonello, A.; Cavalli, A.; Bolognest, M. L.; Minarint, A.; Marucci, G.; Leonardi, A.; Melchiorre, C. Prazosin-related compounds: Effect of transforming the piperazinylquinazoline moiety into an aminomethyltetrahydroacridine system on the affinity for a1-adrenoreceptors. J. Med. Chem. 2003, 46, 4895.
Synthesis and antitumor activity of conjugates of muramyldipeptide, normuramyldipeptide, and desmuramylpeptides with acridine= acridone derivatives
Dzierzbicka, K.; Kolodziejczyk, A. M.; Wysocka-Skrzela, B.; Mysliwski, A.; Sosnowska, D. Synthesis and antitumor activity of conjugates of muramyldipeptide, normuramyldipeptide, and desmuramylpeptides with acridine= acridone derivatives. J. Med. Chem. 2001, 44, 3606.
Synthesis and antitumor activity of conjugates of muramyldipeptide or normuramyldipeptide with hydroxyacridine= acridone derivatives
Dzierzbicka, K.; Kolodziejczyk, A. M. Synthesis and antitumor activity of conjugates of muramyldipeptide or normuramyldipeptide with hydroxyacridine= acridone derivatives. J. Med. Chem. 2003, 46, 183.
Acridine and acridone derivatives, anticancer properties, and synthetic methods: Where are we now?
Philippe, B.; Johann, B.; Thomas, G.; Martin, T. Acridine and acridone derivatives, anticancer properties, and synthetic methods: Where are we now? Anti-Cancer Agents Med. Chem. 2007, 7 (2), 139.