Abdellatif, M.; MacLellan, W. R.; Schneider, M. D. p21 Ras as a governor of global gene expression. J. Biol. Chem. 1994, 269, 15423-15426; Wiesmüller, L.; Wittinghofer, F. Signal transduction pathways involving Ras. Mini review. Cell Signal 1994, 6, 247-267; Barbacid, M. ras oncogenes: their role in neoplasia. Eur. J. Clin. Invest. 1990, 20, 225-235.
Signal transduction pathways involving Ras. Mini review
Abdellatif, M.; MacLellan, W. R.; Schneider, M. D. p21 Ras as a governor of global gene expression. J. Biol. Chem. 1994, 269, 15423-15426; Wiesmüller, L.; Wittinghofer, F. Signal transduction pathways involving Ras. Mini review. Cell Signal 1994, 6, 247-267; Barbacid, M. ras oncogenes: their role in neoplasia. Eur. J. Clin. Invest. 1990, 20, 225-235.
Abdellatif, M.; MacLellan, W. R.; Schneider, M. D. p21 Ras as a governor of global gene expression. J. Biol. Chem. 1994, 269, 15423-15426; Wiesmüller, L.; Wittinghofer, F. Signal transduction pathways involving Ras. Mini review. Cell Signal 1994, 6, 247-267; Barbacid, M. ras oncogenes: their role in neoplasia. Eur. J. Clin. Invest. 1990, 20, 225-235.
Altered phosphatidylcholine metabolism in C3H10T1/2 cells transfected with the Harvey-ras oncogene
(a) Teegarden, D.; Taparowsky, E. J.; Kent, C. Altered phosphatidylcholine metabolism in C3H10T1/2 cells transfected with the Harvey-ras oncogene. J. Biol. Chem. 1990, 265, 6042-6047.
Inhibition of ChoK is an efficient antitumor strategy for Harvey-, Kirsten-, and N-ras-transformed cells
(c) Ramirez de Molina, A.; Rodríguez-González, A.; Peñalva, V.; Lucas, L.; Lacal, J. C. Inhibition of ChoK is an efficient antitumor strategy for Harvey-, Kirsten-, and N-ras-transformed cells. Biochem. Biophys. Res. Commun. 2001, 285, 873-879.
Regulation of choline kinase activity by Ras proteins involves RaI-GDS and PI3K
(d) Ramírez de Molina, A.; Peñalva, V.; Lucas, L.; Lacal, J. C. Regulation of choline kinase activity by Ras proteins involves RaI-GDS and PI3K. Oncogene 2002, 21, 937-946.
(b) de Certaines, J. D.; Larsen, V. A.; Podo, F.; Carpinelli, G.; Briot, O.; Henriksen, O. In vivo 31P MRS of experimental tumours. NMR Biomed. 1993, 6, 345-365.
Phospholipid metabolites, prognosis and proliferation in human breast carcinoma
(c) Smith, T. A. D.; Bush, C.; Jameson, C.; Titley, J. C.; Leach, M. O.; Wilman, D. E. V.; McCready, V. R. Phospholipid metabolites, prognosis and proliferation in human breast carcinoma. NMR Biomed. 1993, 6, 318-323.
Phosphorylcholine: A novel second messenger essential for mitogenic activity of growth factors
(a) Cuadrado, A.; Carnero, A.; Dolfi, F.; Jiménez, B.; Lacal, J. C. Phosphorylcholine: a novel second messenger essential for mitogenic activity of growth factors. Oncogene 1993, 8, 2959-2968.
Generation of phosphorylcholine as an essential event in the activation of Raf-1 and MAP-Kinases in growth factors/induced mitogenic stimulation
(b) Jiménez, B.; del Peso, L.; Montaner, S.; Esteve, P.; Lacal, J. C. Generation of phosphorylcholine as an essential event in the activation of Raf-1 and MAP-Kinases in growth factors/induced mitogenic stimulation. J. Cell Biochem. 1995, 57, 141-149.
Choline kinase inhibitors as a novel approach for antiproliferative drug design
(c) Hernández-Alcoceba, R.; Saniger, L.; Campos, J.; Núñez, M. C.; Khaless, F.; Gallo, M. A.; Espinosa, A.; Lacal, J. C. Choline kinase inhibitors as a novel approach for antiproliferative drug design. Oncogene 1997, 15, 2289-2301.
A novel mechanism for anticancer drug discovery: In vivo antitumor activity by inhibition of phosphorylcholine production
Hernández-Alcoceba, R.; Fernández, F.; Lacal, J. C. A novel mechanism for anticancer drug discovery: in vivo antitumor activity by inhibition of phosphorylcholine production. Cancer Res. 1999, 59, 3112-3118.
QSAR of 1,1′-(1,2-ethylenebisbenzyl)bis(4-substitutedpyridinium) dibromides as choline kinase inhibitors: A different approach for antiproliferative drug design
Campos, J.; Núñez, M. C.; Rodríguez, V.; Gallo, M. A.; Espinosa, A. QSAR of 1,1′-(1,2-ethylenebisbenzyl)bis(4- substitutedpyridinium) dibromides as choline kinase inhibitors: a different approach for antiproliferative drug design. Bioorg. Med. Chem. Lett. 2000, 10, 767-770.
LUMO energy of model compounds of bispyridinium compounds as an index for the inhibition of choline kinase
Campos, J.; Núñez, M. C.; Rodríguez, V.; Entrena, A.; Hernández-Alcoceba, R.; Fernández, F.; Lacal, J. C.; Gallo, M. A.; Espinosa, A. LUMO energy of model compounds of bispyridinium compounds as an index for the inhibition of choline kinase. Eur. J. Med. Chem. 2001, 36, 215-225.
QSAR-derived choline kinase inhibitors: How rational can antiproliferative drug design be?
Campos, J.; Nuñez, M. C.; Conejo-García, A.; Sánchez-Martín, R. M. Hernández-Alcoceba, R.; Rodríguez-González, A.; Lacal, J. C.; Gallo, M. A.; Espinosa, A. QSAR-derived choline kinase inhibitors: how rational can antiproliferative drug design be? Curr. Med. Chem. 2003, 10, 1095-1112.
Overexpression of choline kinase is a frequent feature in human tumor-derived cell lines and in lung, prostate, and colorectal human cancers
Ramírez de Molina, A.; Rodríguez-González, A.; Gutiérrez, R.; Martínez-Piñero, L.; Sánchez, J. J.; Bonilla, F.; Rosell, R.; Lacal, J. C. Overexpression of choline kinase is a frequent feature in human tumor-derived cell lines and in lung, prostate, and colorectal human cancers. Biochem. Biophys. Res. Commun. 2002, 296, 580-583.
Choline kinase inhibitory effect and antiproliferative activity of new 1,1′,1″-(benzene-1,3,5-triylmethylene)tris{4-[(disubstituted)amino] pyridinium} tribromides
Conejo-García, A.; Campos, J.; Sánchez, R. M.; Rodríguez-González, A.; Juan C. Lacal, Gallo, M. A.; Espinosa, A. Choline kinase inhibitory effect and antiproliferative activity of new 1,1′,1″-(benzene-1,3,5-triylmethylene)tris{4-[(disubstituted)amino] pyridinium} tribromides. Eur. J. Med. Chem. 2003, 38, 109-116.
Bispyridmium cyclophanes: Novel templates for human choline kinase inhibitors
Conejo-García, A.; Campos, J. M.; Sánchez-Martín, R. M.; Gallo, M. A.; Espinosa, A. Bispyridmium cyclophanes: novel templates for human choline kinase inhibitors. J. Med. Chem. 2003, 46, 3754-3757.
Conformational dynamics of a bispyridinium cyclophane
Conejo-García, A.; Campos, J. M.; Entrena, A.; Sánchez-Martín, R. M.; Gallo, M. A.; Espinosa, A. Conformational dynamics of a bispyridinium cyclophane. J. Org. Chem. 2003, 68, 8697-8699.
Influence of the linker in bispyridinium compounds on the inhibition of human choline kinase
Conejo-García, A.; Báñez-Coronel, M.; Sánchez-Martín, R. M.; Rodríguez-González, A.; Ramos, A.; Ramírez de Molina, A.; Espinosa, A.; Gallo, M. A.; Campos, J. M.; Lacal, J. C. Influence of the linker in bispyridinium compounds on the inhibition of human choline kinase. J. Med. Chem. 2004, 47, 5433-5440.
Towards a model for the inhibition of choline kinase by a new type of inhibitor
Conejo-García, A.; Entrena, A.; Campos, J. M.; Sánchez-Martín, R. M.; Gallo, M. A.; Espinosa, A. Towards a model for the inhibition of choline kinase by a new type of inhibitor. Eur. J. Med. Chem. 2004, 315-319.
Relative ease of cyclization of 2-, 3- and 4-aminopyridine derivatives. Synthesis of naphthyridines
Hauser, C. R.; Reynolds, G. A. Relative ease of cyclization of 2-, 3- and 4-aminopyridine derivatives. Synthesis of naphthyridines. J. Org. Chem. 1950, 15, 1224-1232.
Synthesis and quantitative structure-activity relationships of dequalinium analogues as K+ channel blockers: Investigation into the role of the substituent at position 4 of the quinoline ring
Galanakis, D.; Calder, J.; Ganellin, C. R.; Owen, C. S.; Dunn, P. M. Synthesis and quantitative structure-activity relationships of dequalinium analogues as K+ channel blockers: investigation into the role of the substituent at position 4 of the quinoline ring. J. Med. Chem. 1995, 38, 3536-3546.
Structural specificity of chloroquine-hematin binding related to inhibition of hematin polymerization and parasite growth
Vippagunta, S. R.; Dorn, A.; Matile, H.; Bhattacharjee, A. K.; Karle, J. M.; Ellis, W. Y.; Ridley, R. G.; Vennerstrom, J. L. Structural specificity of chloroquine-hematin binding related to inhibition of hematin polymerization and parasite growth. J. Med. Chem. 1989, 42, 4630-4639.
The reaction of activated aryl and heteroaryl dihalides with HMPA. A regioselectivity study
Gupton, J. T.; Wysong, E.; Norman, B.; Hertel, G.; Idoux, J. P. The reaction of activated aryl and heteroaryl dihalides with HMPA. A regioselectivity study. Synth. Commun. 1985, 15, 43-52.
Synthesis and antibacterial activity of new 4-alkoxy, 4-aminoalkyl and 4-alkylthioquinoline derivatives
Kayirere, M.-G.; Mahamoud, A.; Chevalier, J.; Soyfer, J.-C.; Crémieux, A.; Barbe, J. Synthesis and antibacterial activity of new 4-alkoxy, 4-aminoalkyl and 4-alkylthioquinoline derivatives. Eur. J. Med. Chem. 1998, 33, 55-64.
Konstitution und eigenschaften des biphenylen-(4,4′)-bis- [methylatropiniumbromids], einer biquartären atropinverbindung
Szendey, G. L.; Munnes, S. Konstitution und eigenschaften des biphenylen-(4,4′)-bis-[methylatropiniumbromids], einer biquartären atropinverbindung. (Constitution and properties of biphenylene-(4,4′)- bis[methylatropinium] bromide, a bisquaternary atropine compound). Chem. Ber. 1881, 94, 38-42.
Synthesen won [2.2](4,4′)biphenylophan, [2.2](2,7)phenanthrenophan und [2](4,4′)biphenylo[2](2,7)-phenanthrenophan
Staab, H. A.; Haenel, M. Synthesen won [2.2](4,4′)biphenylophan, [2.2](2,7)phenanthrenophan und [2](4,4′)biphenylo[2](2,7)- phenanthrenophan. Chem. Ber. 1973, 106, 2190-2202.
Synthesis, molecular modeling, and K+ channel-blocking activity of dequalinium analogues having semirigid linkers
Campos Rosa, J.; Galanakis, D.; Ganellin, C. R.; Dunn, P. M. Synthesis, molecular modeling, and K+ channel-blocking activity of dequalinium analogues having semirigid linkers. J. Med. Chem. 1996, 39, 4247-4254.
Macdonald, J. S., Haller, D. G., Mayer, R. J., Eds.; J. B. Lippincott Co.: Philadelphia
Schnall, S.; Macdonald, J. S. In Manual of Oncologic Therapeutics; Macdonald, J. S., Haller, D. G., Mayer, R. J., Eds.; J. B. Lippincott Co.: Philadelphia, 1995; pp. 170-184.
Atomic physicochemical parameters for three-dimensional structure directed quantitative structure-activity relationships. 4. Additional parameters for hydrophobic and dispersive interactions and their application for an automated superposition of certain naturally occurring nucleoside antibiotics
Viswanadhan, V. N.; Ghose, A. K.; Revankar, G. R.; Robins, P. K. Atomic physicochemical parameters for three-dimensional structure directed quantitative structure-activity relationships. 4. Additional parameters for hydrophobic and dispersive interactions and their application for an automated superposition of certain naturally occurring nucleoside antibiotics. J. Chem. Inf. Comput. Sci. 1989, 29, 163-172.
PALLAS FRAME MODULE, a prediction tool of physicochemical parameters, is supplied by CompuDrug Chemistry, Ltd, PO Box 23196, Rochester, NY 14692.
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0002370147
QSAR hansch analysis and related approaches
Mannhold, R., Krogsgaard-Larsen, P., Timmerman, H., Eds.; VCH: Weinheim
Kubinyi, H. QSAR: Hansch Analysis and Related Approaches. In Methods and Principles in Medicinal Chemistry; Mannhold, R., Krogsgaard-Larsen, P., Timmerman, H., Eds.; VCH: Weinheim. 1993: Vol. 1, pp 40-41.
(Ramsden, C. A., Ed.); Hansch, C., Sammes, P. G., Taylor, J. B., Eds.; Pergamon Press: Oxford
Blaney, J. M.; Hansch, C. Quantitative Drug Design (Ramsden, C. A., Ed.). In Comprehensive Medicinal Chemistry. The Rational Design, Mechanistic Study & Terapeutic Application of Chemical Compounds; Hansch, C., Sammes, P. G., Taylor, J. B., Eds.; Pergamon Press: Oxford, 1990; Vol. 4, pp 459-496.
Seydel J. K., Schaper, K.-J., Eds.; Verlag Chemie: Weinheim
Hansch, C. Blaney, J. M. Chemische Struktur und biologische Aktivität von Wirkstoffen. Methoden der Quantitativen Struckutr-Wirkung- Analyse; Seydel J. K., Schaper, K.-J., Eds.; Verlag Chemie: Weinheim, 1979; pp 185-208.
Quantitative structure-activity relationships for a series of symmetrical bisquaternary anticancer compounds
Campos, J. M.; Núñez, M. C.; Sánchez, R. S.; Gómez-Vidal, J. A.; Rodríguez-González, A.; Báñez, M.; Gallo, M. A.; Lacal, J. C.; Espinosa, A. Quantitative structure-activity relationships for a series of symmetrical bisquaternary anticancer compounds. Bioorg. Med. Chem. 2002, 10, 2215-2231.
Modulation of phospholipase D by hexadecylphosphorylcholine: A putative novel mechanism for its antitumoral activity
Lucas, L.; Hernández-Alcoceba, R.; Rodríguez, P.; Lacal, J. C. Modulation of phospholipase D by hexadecylphosphorylcholine: a putative novel mechanism for its antitumoral activity. Oncogene 2001, 20, 1110-1117.
Regulation of choline kinase activity by Ras proteins involves RaI-GDS and PI3K
Ramírez de Molina, A.; Peñalva, V.; Lucas, L.; Lacal, J. C. Regulation of choline kinase activity by Ras proteins involves RaI-GDS and PI3K. Oncogene 2002, 21, 937-946.