Аннотация:
The reactions of methylpheophorbide a with primary and secondary amines have been investigated as a means for the synthesis of sensitizers used in the photodynamic therapy of tumors
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
D. V. Belykh, L. P. Karmanova, L. V. Spirikhin, A. V. Kutchin, “Synthesis of chlorin e6 amide derivatives”, Mendeleev Commun., 12:2 (2002), 77–78
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4100
https://www.mathnet.ru/rus/mendc/v12/i2/p77
Эта публикация цитируется в следующих 31 статьяx:
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L. A. Tulaeva, E. I. Pushkareva, O. V. Tolstikova, D. V. Belykh, “Exo ring opening in methyl pheophorbide a 132-amide derivatives under the action of amines”, Russ Chem Bull, 70:2 (2021), 359
D. V. Belykh, “C–O, C–S, C–N, and C–C Bond Formation at the Periphery of the Macrocycle during Chemical Modification of Phytochlorins: Key Methods and Synthetic Applications”, Russ J Gen Chem, 89:12 (2019), 2604
Dmitrii V. Belykh, Lidiya I. Mazaletskaya, Nataliya I. Sheludchenko, Tatyana K. Rocheva, Irina S. Khudyaeva, Evgeny V. Buravlev, Olga V. Shchukina, Irina Yu. Chukicheva, “Antiradical Activity of Porphyrins with a Diisobornylphenol Fragment at the Macrocycle Periphery”, Molecules, 23:7 (2018), 1718
M. A. Gradova, I. I. Ostashevskaya, O. V. Gradov, A. V. Lobanov, V. S. Lebedeva, A. F. Mironov, “Photophysical properties and photodynamic activity of 13,15-N-methoxy-cycloimide chlorin p6 methyl ester in micellar surfactant solutions”, Mendeleev Commun., 28:6 (2018), 589–591
Elnaz Yaghini, Ruggero Dondi, Kunal M. Tewari, Marilena Loizidou, Ian M. Eggleston, Alexander J. MacRobert, “Endolysosomal targeting of a clinical chlorin photosensitiser for light-triggered delivery of nano-sized medicines”, Sci Rep, 7:1 (2017)
Hitoshi Tamiaki, Keisuke Mizutani, Shin-ichi Sasaki, Tomohiro Tatebe, “Rotational isomerization of 3-substituents in synthetic chlorophyll derivatives”, Tetrahedron, 72:42 (2016), 6626
Yuri N. Antonenko, Elena A. Kotova, Elena O. Omarova, Tatyana I. Rokitskaya, Valentina A. Ol'shevskaya, Valery N. Kalinin, Roza G. Nikitina, Julia S. Osipchuk, Mikhail A. Kaplan, Alla A. Ramonova, Mikhail M. Moisenovich, Igor I. Agapov, Mikhail P. Kirpichnikov, “Photodynamic activity of the boronated chlorin e6 amide in artificial and cellular membranes”, Biochimica et Biophysica Acta (BBA) - Biomembranes, 1838:3 (2014), 793
Gelii V. Ponomarev, Maria N. Solovieva, Nikita O. Dugin, Maria G. Zavialova, Arif R. Mehtiev, Alexander Yu. Misharin, Roman A. Novikov, Yaroslav V. Tkachev, Vladimir I. Popenko, Vladimir P. Timofeev, “Lipophilic derivatives of natural chlorins: Synthesis, mixed micelles with phospholipids, and uptake by cultured cells”, Bioorganic & Medicinal Chemistry, 21:17 (2013), 5420
N. V. S. Dinesh K. Bhupathiraju, M. Graça H. Vicente, Topics in Heterocyclic Chemistry, 34, Applications of Porphyrinoids, 2013, 31
D. V. Belykh, E. V. Buravlev, M. V. Malˈshakova, N. N. Parshukova, E. A. Kopylov, I. V. Gruzdev, A. V. Kuchin, “Reaction of methylpheophorbides d and b with amines”, Chem Nat Compd, 47:1 (2011), 85
M. V. Mal'shakova, D. V. Belykh, V. M. Hudyaev, A. V. Kuchin, “Synthesis of amide-bonded chlorin dimers and trimers without the use of activating agents”, Dokl Chem, 436:2 (2011), 19
D. V. Belykh, M. V. Mal'shakova, Yu. A. Yudina, K. A. Zavadskaya, V. M. Khudyaev, A. V. Kuchin, “Synthesis of potential antitumor agents, dimeric and trimeric chlorins, from methylpheophorbide a”, Russ Chem Bull, 60:4 (2011), 719
D. V. Belykh, E. I. Pushkareva, “Amidation of the ester group of methylpheoforbide a with sterically nonhindered primary and secondary aliphatic amines”, Russ J Gen Chem, 81:6 (2011), 1216
M. A. Grin, R. A. Titeev, D. I. Brittal, O. V. Ulybina, A. G. Tsiprovskiy, M. Ya. Berzina, I. A. Lobanova, I. B. Sivaev, V. I. Bregadze, A. F. Mironov, “New conjugates of cobalt bis(dicarbollide) with chlorophyll a derivatives”, Mendeleev Commun., 21:2 (2011), 84–86
D. V. Belykh, E. A. Kopylov, I. V. Gruzdev, A. V. Kuchin, “Opening of the extra ring in pheophorbide a methyl ester by the action of amines as a one-step method for introduction of additional fragments at the periphery of chlorin macroring”, Russ J Org Chem, 46:4 (2010), 577
D. V. Belykh, E. V. Buravlev, P. A. Slepukhin, A. V. Kuchin, “Atropoisomerism of 13-N,N-dimethylamide-15,17-dimethyl ester of chlorin e 6 from the data of X-ray, 1H NMR, and HPLC”, Russ J Gen Chem, 80:11 (2010), 2382
D. V. Belykh, I. S. Tarabukina, I. V. Gruzdev, A. V. Kuchin, “Transformations of the extra ring in pheophorbide a methyl ester in the reaction with N,N,N′,N′-tetramethylmethanediamine”, Russ J Org Chem, 45:3 (2009), 452
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A. V. Kuchin, M. V. Mal'shakova, D. V. Belykh, V. A. Ol'shevskaya, V. N. Kalinin, “Synthesis of boronated derivatives of chlorin e6 with amide bond”, Dokl Chem, 425:2 (2009), 80