Abstract:
The organophosphorus analogues of the biologically significant sulfonium compounds S-adenosylmethionine and S-methylmethionine are much more stable than their carboxylic prototypes.
Document Type:
Article
Language: English
Citation:
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
Linking options:
https://www.mathnet.ru/eng/mendc4044
https://www.mathnet.ru/eng/mendc/v13/i6/p243
This publication is cited in the following 7 articles:
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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