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  • 1
    Killmer, L., F. G. Vogt, A. J. Freyer, M. D. Menachery and C. M. Adelman (2003) Lakshminine, a new rare oxoisoaporphine alkaloid from Sciadotenia toxifera, and structural revisions of telazoline and teladiazoline, two related oxoaporphines from Telitoxicum peruvianum and T-glaziovii. J. Nat. Prod. 66, 115118.
  • 2
    Sugimoto, Y., H. A. A. Babiker, S. Inanaga, M. Kato and A. Isogai (1999) Oxoisoaporphines from Menispermum dauricum. Phytochemistry 52, 14311435.
  • 3
    Yu, B. W., L. H. Meng, J. Y. Chen, T. X. Zhou, K. F. Cheng, J. Ding and G. W. Qin (2001) Cytotoxic oxoisoaporphine alkaloids from Menispermum dauricum. J. Nat. Prod. 64, 968970.
  • 4
    Flors, C. and S. Nonell (2006) Light and singlet oxygen in plant defense against pathogens: Phototoxic phenalenone phytoalexins. Accounts. Chem. Res. 39, 293300.
  • 5
    Flors, C., P. R. Ogilby, J. G. Luis, T. A. Grillo, L. R. Izquierdo, P. L. Gentili, L. Bussotti and S. Nonell (2006) Phototoxic phytoalexins. Processes that compete with the photosensitized production of singlet oxygen by 9-phenylphenalenones. Photochem. Photobiol. 82, 95103.
  • 6
    Schmidt, R., C. Tanielian, R. Dunsbach and C. Wolff (1994) Phenalenone, a universal reference compound for the determination of quantum yields of singlet oxygen O2(1Δg) sensitization. J. Photoch. Photobio. A 79, 1117.
  • 7
    Martí, C., O. Jürgens, O. Cuenca, M. Casals and S. Nonell (1996) Aromatic ketones as standards for singlet molecular oxygen O2(1Δg) photosensitization. Time-resolved photoacoustic and near-IR emission studies. J. Photoch. Photobio. A 97, 1118.
  • 8
    Lazzaro, A., M. Corominas, C. Marti, C. Flors, L. R. Izquierdo, T. A. Grillo, J. G. Luis and S. Nonell (2004) Light- and singlet oxygen-mediated antifungal activity of phenylphenalenone phytoalexins. Photoch. Photobio. Sci. 3, 706710.
  • 9
    Flors, C., C. Prat, R. Suau, F. Najera and S. Nonell (2005) Photochemistry of phytoalexins containing phenalenone-like chromophores: Photophysics and singlet oxygen photosensitizing properties of the plant oxoaporphine alkaloid oxoglaucine. Photochem. Photobiol. 81, 120124.
  • 10
    Castro-Castillo, V., M. Rebolledo-Fuentes, C. Theoduloz and B. K. Cassels (2010) Synthesis of lakshminine and antiproliferative testing of related oxoisoaporphines. J. Nat. Prod. 73, 19511953.
  • 11
    Castro-Castillo, V., C. Suarez-Rozas, A. Pabon, E. G. Perez, B. K. Cassels and S. Blair (2013) Synthesis and antiplasmodial activity of some 1-azabenzanthrone derivatives. Bioorgan. Med. Chem. Lett. 23, 327329.
  • 12
    Prado-Prado, F., X. Garcia-Mera, M. Escobar, E. Sobarzo-Sanchez, M. Yanez, P. Riera-Fernandez and H. Gonzalez-Diaz (2011) 2D MI-DRAGON: A new predictor for protein-ligands interactions and theoretic-experimental studies of US FDA drug-target network, oxoisoaporphine inhibitors for MAO-A and human parasite proteins. Eur. J. Med. Chem. 46, 58385851.
  • 13
    Dzieduszycka, M., S. Martelli, M. Arciemiuk, M. M. Bontemps-Gracz, A. Kupiec and E. Borowski (2002) Effect of modification of 6-[(Aminoalkyl)amino]-7H-benzo[e]-perimidin-7-ones on their cytotoxic activity toward sensitive and multidrug resistant tumor cell lines. Synthesis and biological evaluation. Bioorgan. Med. Chem. 10, 10251035.
  • 14
    Bu, X., J. Chen, L. W. Deady, C. L. Smith, B. C. Baguley, D. Greenhalgh, S. Yang and W. A. Denny (2005) Synthesis and cytotoxic activity of N-[(alkylamino)alkyl]carboxamide derivatives of 7-oxo-7H-benz[de]anthracene, 7-oxo-7H-naphtho[1,2,3-de]quinoline, and 7-oxo-7H-benzo[e]perimidine. Bioorgan. Med. Chem. 13, 36573665.
  • 15
    Stefanska, B., M. Dzieduszycka, S. Martelli, J. Tarasiuk, M. Bontempsgracz and E. Borowski (1993) 6-[(Aminoalkyl)Amino]-substituted 7H-benzo[E]perimidin-7-ones as novel antineoplastic agents – Synthesis and biological evaluation. J. Med. Chem. 36, 3841.
  • 16
    Stefanska, B., M. Dzieduszycka, M. M. Bontemps-Gracz, E. Borowski, S. Martelli, R. Supino, G. Pratesi, M. De Cesare, F. Zunino, H. Kusnierczyk and C. Radzikowski (1999) 8,11-dihydroxy-6-[(aminoalkyl)amino]-7H-benzo[e]perimidin-7-ones with activity in multidrug-resistant cell lines: Synthesis and antitumor evaluation. J. Med. Chem. 42, 34943501.
  • 17
    Borovlev, I. V., O. P. Demidov, A. V. Aksenov and A. F. Pozharskii (2004) Heterocyclic analogs of pleiadiene: LXXIV. peri-cyclizations in the perimidine series. Synthesis of 1,3-diazapyrene derivatives. Russ. J. Org. Chem+. 40, 895901.
  • 18
    Tang, H., X. D. Wang, Y. B. Wei, S. L. Huang, Z. S. Huang, J. H. Tan, L. K. An, J. Y. Wu, A. S. C. Chan and L. Q. Gu (2008) Oxoisoaporphine alkaloid derivatives: Synthesis, DNA binding affinity and cytotoxicity. Eur. J. Med. Chem. 43, 973980.
  • 19
    Tang, H., F.-X. Ning, Y.-B. Wei, S.-L. Huang, Z.-S. Huang, A. S.-C. Chan and L.-Q. Gu (2007) Derivatives of oxoisoaporphine alkaloids: A novel class of selective acetylcholinesterase inhibitors. Bioorg. Med. Chem. Lett. 17, 37653768.
  • 20
    Aliaga, C., M. Cerón-Neculpán, C. Saitz, C. Jullian, E. Sobarzo-Sánchez and J. R. De la Fuente (2011) Oxoisoaporphines: Regioselective deuterium labelling involving the metastable hydrogenated photoproduct anions. J. Photoch. Photobio. A 222, 360365.
  • 21
    De la Fuente, J. R., C. Jullian, C. Saitz, V. Neira, O. Poblete and E. Sobarzo-Sanchez (2005) Unexpected formation of 1-diethylaminobutadiene in photosensitized oxidation of triethylamine induced by 2,3-dihydro-oxoisoaporphine dyes. A H1 NMR and isotopic exchange study. J. Org. Chem. 70, 87128716.
  • 22
    De la Fuente, J. R., V. Neira, C. Saitz, C. Jullian and E. Sobarzo-Sanchez (2005) Photoreduction of oxoisoaporphine dyes by amines: Transient-absorption and semiempirical quantum-chemical studies. J. Phys. Chem. A 109, 58975904.
  • 23
    De la Fuente, J. R., C. Jullian, C. Saitz, E. Sobarzo-Sanchez, V. Neira, C. Gonzalez, R. Lopez and H. Pessoa-Mahana (2004) Photoreduction of oxoisoaporphines. Another example of a formal hydride-transfer mechanism. Photoch. Photobio. Sci. 3, 194199.
  • 24
    De la Fuente, J. R., C. Aliaga, C. Poblete, G. Zapata, C. Jullian, C. Saitz, A. Cañete, G. Kciuk, E. Sobarzo-Sanchez and K. Bobrowski (2009) Photoreduction of oxoisoaporphines by amines: Laser flash and steady-state photolysis, pulse radiolysis, and TD-DFT studies. J. Phys. Chem. A, 113, 77377747.
  • 25
    Bu, X., L. W. Deady, G. J. Finlay, B. C. Baguley and W. A. Denny (2001) Synthesis and cytotoxic activity of 7-oxo-7H-dibenz[f, ij]isoquinoline and 7-Oxo-7H-benzo[e]perimidine derivatives. J. Med. Chem. 44, 20042014.
  • 26
    De la Fuente, J. R., G. Kciuk, E. Sobarzo-Sanchez and K. Bobrowski (2008) Transient phenomena in the pulse radiolysis of oxoisoaporphine derivatives in acetonitrile. J. Phys. Chem. A 112, 1016810177.
  • 27
    De la Fuente, J. R., E. Sobarzo-Sanchez and K. Bobrowski (2006) Spectroscopic Characterization of Radical Species from 2,3 dihydro-oxoisoaporphines Generated by Flash Photolysis and Pulse Radiolysis. Proceedings of the 18th Conference on Physical Organic Chemistry, Warsaw University, Poland.
  • 28
    De la Fuente, J. R., A. Cañete, C. Saitz and C. Jullian (2002) Photoreduction of 3-phenylquinoxalin-2-ones by amines: Transient-absorption and semiempirical quantum-chemical studies. J. Phys. Chem. A 106, 71137120.
  • 29
    Viteri, G., A. M. Edwards, J. De la Fuente and E. Silva (2003) Study of the interaction between triplet riboflavin and the α-, β(H)- and β(L)-crystallins of the eye lens. Photochem. Photobiol. 77, 535540.
  • 30
    Mirkowski, J., P. Wisniowski and K. Bobrowski (2001) In INCT Annual Report 2000, (Edited by INCT), pp. 3133. INCT, Warsaw.
  • 31
    Bobrowski, K. (2005) Free radicals in chemistry, biology, and medicine: contribution of radiation chemistry. Nukleonika 50(Suppl 3), S67S76.
  • 32
    Bobrowski, K., G. Dzierzkowska, J. Grodkowski, Z. Stuglik, Z. P. Zagorski and W. L. McLaughlin (1985) A pulse radiolysis study of the leucocyanide of malachite green dye in organic solvents. J. Phys. Chem. 89, 43584366.
  • 33
    Boule, P. and J. F. Pilichowski (1993) Comments about the use of aberchrome (Tm)-540 in chemical actinometry. J. Photoch. Photobio. A 71, 5153.
  • 34
    Reichardt, C. (1990) Solvents and Solvent Effects in Organic Chemistry. VCH, New York.
  • 35
    Sobarzo-Sánchez, E., P. G. Soto, C. Valdés Rivera, G. Sánchez and M. E. Hidalgo (2012) Applied biological and physicochemical activity of isoquinoline alkaloids: Oxoisoaporphine and boldine. Molecules 17, 1095810970.
  • 36
    Sobarzo-Sánchez, E. and E. U. Villares (2011) Patent ES 2357926 Type A1. Preparation of nitrogen based heterocycles for the production of oxygen singlets.. Universidad de Santiago de Compostela, Spain.
  • 37
    Murov, S. L., I. Carmichael and G. L. Hug (1993) Handbook of Photochemistry. Dekker, New York.
  • 38
    Brede, O., D. Beckert, C. Windolph and H. A. Gottinger (1998) One-electron oxidation of sterically hindered amines to nitroxyl radicals: Intermediate amine radical cations, aminyl, alpha-aminoalkyl, and aminylperoxyl radicals. J. Phys. Chem. A 102, 14571464.