Аннотация:
The title compounds were prepared in high overall yields from properly protected (Boc, Cbz) 2- , 3- or 8-methyl-4-azaoctane-1,8-diamines. N1-Acetyl-2-methyl- and N1-acetyl-8-methylspermidines, but not N1-acetyl-3-methylspermidine, were the substrates for N1-acetylpolyamine oxidase.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
M. A. Khomutov, M. T. Hyvönen, A. R. Simonian, J. Weisell, J. J. Vepsalainen, L. Alhonen, S. N. Kochetkov, T. A. Keinanen, A. R. Khomutov, “Acetylated derivatives of C-methylated analogues of spermidine: synthesis and interaction with N1-acetylpolyamine oxidase”, Mendeleev Commun., 28:5 (2018), 479–481
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1806
https://www.mathnet.ru/rus/mendc/v28/i5/p479
Эта публикация цитируется в следующих 5 статьяx:
M. A. Khomutov, A. R. Khomutov, “Synthesis of 2-Methylidene Spermidine and its N1-Acetylated Derivative”, Russ J Bioorg Chem, 48:6 (2022), 1202
Maxim Khomutov, Mervi T. Hyvönen, Alina Simonian, Andrey A. Formanovsky, Irina V. Mikhura, Alexander O. Chizhov, Sergey N. Kochetkov, Leena Alhonen, Jouko Vepsäläinen, Tuomo A. Keinänen, Alex R. Khomutov, “Unforeseen Possibilities To Investigate the Regulation of Polyamine Metabolism Revealed by Novel C-Methylated Spermine Derivatives”, J. Med. Chem., 62:24 (2019), 11335
M. A. Khomutov, I. V. Mikhura, S. N. Kochetkov, A. R. Khomutov, “C-Methylated Analogs of Spermine and Spermidine: Synthesis and Biological Activity”, Russ J Bioorg Chem, 45:6 (2019), 463
K. A. Perevoshchikova, A. I. Nichugovskiy, A. K. Isagulieva, N. G. Morozova, I. V. Ivanov, M. A. Maslov, A. A. Shtil, “Synthesis of novel lipophilic tetraamines with cytotoxic activity”, Mendeleev Commun., 29:6 (2019), 616–618
M. A. Khomutov, A. O. Chizhov, S. N. Kochetkov, A. R. Khomutov, “Synthesis of (R)- and (S)-isomers of 2-methylspermidine”, Mendeleev Commun., 29:6 (2019), 678–679