Abstract:
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.
Document Type:
Article
Language: English
Citation:
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
Linking options:
https://www.mathnet.ru/eng/mendc1806
https://www.mathnet.ru/eng/mendc/v28/i5/p479
This publication is cited in the following 5 articles:
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