Аннотация:
The organophosphorus analogues of the biologically significant sulfonium compounds S-adenosylmethionine and S-methylmethionine are much more stable than their carboxylic prototypes.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
K. V. Alferov, Yu. N. Zhukov, E. N. Khurs, R. M. Khomutov, “Stable organophosphorus analogues of S-adenosylmethionine and S-methylmethionine”, Mendeleev Commun., 13:6 (2003), 243–244
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4044
https://www.mathnet.ru/rus/mendc/v13/i6/p243
Эта публикация цитируется в следующих 7 статьяx:
K. A. Kochetkov, M. A. Tsvetikova, O. N. Gorunova, N. A. Bystrova, V. S. Yufriakov, “Enantioselective synthesis of 5-fluoro-L-DOPA via chemoenzymatic route”, Mendeleev Commun., 34:1 (2024), 11–12
V. L. Filonov, M. A. Khomutov, A. V. Sergeev, A. L. Khandazhinskaya, S. N. Kochetkov, E. S. Gromova, A. R. Khomutov, “Interaction of DNA Methyltransferase Dnmt3a with Phosphorus Analogues of S-Adenosylmethionine and S-Adenosylhomocysteine”, Molekulârnaâ biologiâ, 57:4 (2023), 717
V. L. Filonov, M. A. Khomutov, A. V. Sergeev, A. L. Khandazhinskaya, S. N. Kochetkov, E. S. Gromova, A. R. Khomutov, “Interaction of DNA Methyltransferase Dnmt3a with Phosphorus Analogs of S-Adenosylmethionine and S-Adenosylhomocysteine”, Mol Biol, 57:4 (2023), 747
A. Yu. Rudenko, S. S. Mariasina, P. V. Sergiev, V. I. Polshakov, “Analogs of S-Adenosyl-L-Methionine in Studies of Methyltransferases”, Mol Biol, 56:2 (2022), 229
R. M. Khomutov, A. I. Shchipanova, E. N. Khurs, “Phosphoanalogues of amino acids involved in methionine metabolism as a new source of antiviral compounds”, Dokl Biochem Biophys, 425:1 (2009), 84
Marta Zarandi, Amino Acids, Peptides and Proteins, 2007, 19
Kirill V. Alferov, Yurii N. Zhukov, Elena N. Khurs, Radii M. Khomutov, “Stable Organophosphorus Analogues of S‐Adenosylmethionine and S‐Methylmethionine.”, ChemInform, 35:20 (2004)
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