Peptide derivatives of tylosin-related macrolides

Russian Journal of Bioorganic Chemistry

Volumn 33, Issue 2, 2007, Pages 218-226

  Korshunova, G A ^a   Sumbatyan, N V ^a   Fedorova, N V ^a   Kuznetsova, I V ^a   Shishkina, A V ^a   Bogdanov, A A ^a  

^a MOSCOW STATE UNIVERSITY   (Russian Federation)

Author keywords

Desmycosin; O mycaminosyltylonolide; Peptide derivatives of macrolides; Tylosin

Indexed keywords

EID: 34247223610     PISSN: 10681620     EISSN: None     Source Type: Journal    
DOI: 10.1134/S1068162007020033     Document Type: Article

References (25)

1. Gale, E.F., Candliffe, E., Reynolds, P.E., Richmond, M.H., and Waring, M.J., The Molecular Basis of Antibiotic Action, London: John Wiley and Sons, 1981.
2. Hansen, J.L., Ippolito, A., Ban, N., Nissen, P., Moore, P.B., and Steitz, A., Mol. Cell, 2002, vol. 10, pp. 117-128.
3. Schlunzen, F., Zarivach, R., Harms, J., Bashan, A., Tocilj, A., Albrecht, R., Yonath, A., and Franceschi, F., Nature, 2001, vol. 413, pp. 814-821.
4. Schlunzen, F., Harms, J., Franceschi, F., Hansen, H.A., Bartels, H., Zarivach, R., and Yonath, A., Structure, 2003, vol. 11, pp. 329-338.
5. Bogdanov, A.A., Mol. Biol. (Moscow), 2003, vol. 37, pp. 1-4.
6. Sumbatyan, N.V., Korshunova, G.A., and Bogdanov, A.A., Biokhimiya (Moscow), 2003, vol. 68, pp. 1436-1438.
7. Hamill, R.L., Haney, M.E., McGuire, J.M., and Stamper, M.C., US Patent 3178341, 1965.
8. Morin, R. and Gorman, M., US Patent 3 459 853, 1969.
9. Tanaka, A., Watanabe, A., Tsuchiya, T., and Umezawa, S., J. Antibiot., 1981, vol. 34, pp. 1381-1384.
10. Gisin, B.F., Helv. Chim. Acta, 1973, vol. 56, pp. 1476-1482.
11. Kirst, H., GB Patent 2111497, 1983
12. Kirst, H. and Toth, J., US Patent 4459290, 1984.
13. Finkel'shtein, A.V. and Ptitsyn, O.B., Fizika belka: Kurs lektsii (Physics of Proteins: A Course of Lectures), 3rd Ed., Moscow: Knizhnyi dom Universitet, 2005.
14. Konig, W. and Geiger, R., Chem. Ber., 1970, vol. 103, pp. 788-798.
15. Wang, S.S., Gisin, B.F., Winter, D.P., Makofske, R., Kulesha, I.D., Tzograki, C., and Meienhofer, I., J. Org. Chem., 1977, vol. 42, pp. 1286-1290.
16. Merrifield, R.B., J. Am. Chem. Soc., 1963, vol. 85, pp. 2149-2154.
17. Kohli, V., Blocker, H., and Koster, H., Tetrahedron Lett., 1980, vol. 21, pp. 2683-2686.
18. Jian, T., Phanly, T., Busuyek, M., Hou, Y., Or, Y., Qiu, Y., and Vo, N., US Patent 6753415 B2, 2003.
19. Fujiwara, T., Watanabe, H., Hirano, T., and Sakakibara, H., GB Patent 2116170A, 1983.
20. Sheehan, J.C. and Hess, G.P., J. Am. Chem. Soc., 1955, vol. 77, pp. 1067-1068.
21. Kessler, H. and Siegmeier, R., Tetrahedron Lett., 1983, vol. 24, pp. 281-282.
22. McDermott, J.R. and Benoiton, N.L., Can. J. Chem., 1973, vol. 51, pp. 2555-2561.
23. Knorr, R., Trzeciak, A., Bannwarth, W., and Gillessen, D., Tetrahedron Lett., 1989, vol. 30, pp. 1927-1932.
24. Medvedkin, V.N., Zabolotskikh, V.F., Permyakov, E.A., Mitin, Yu.V., Sorokina, M.N., and Klimenko, L.V., Bioorg. Khim., 1995, vol. 21, pp. 684-690.
25. Kaiser, E., Colescott, R.L., Bossinger, C.D., and Cook, P.I., Anal. Biochem., 1970, vol. 34, pp. 595-598.