Abstract
1,2-Tritium-labeled 3-(O-carboxypropyl)- and 3-(O-carbomethoxypropyl)-oximes of 6α-methyl-16α,17α-cyclohexanopregn-4-ene-3,20-diones were obtained by the homogeneous catalytic hydrogenation of 1,2-dehydroprecursors with gaseous tritium and the subsequent separation of the resulting mixtures by HPLC. The specific radioactivities of 50–55 Ci/mmol were prepared using tris-(triphenylphosphine)-rhodium chloride.
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Abbreviations
- UT:
-
uterine pentaranophilin
- PR:
-
progesterone receptor
References
Smirnov, A.N., (Element of Endocrine Regulation), Moscow: GEODAR-Media, 2006 [in Russian].
Smirnov, A.N., Pokrovskaya, E.V., Shevchenko, V.P., Levina, I.S., and Kamernitskii, A.V., Bioorg. Khim., 1999, vol. 25, pp. 774–781.
Smirnov, A.N., Pokrovskaya, E.V., Kogteva, G.S., Shevchenko, V.P., Levina, I.S., Kulikova, L.E., and Kamernitzky, A.V., Steroids, 2000, vol. 65, pp. 163–170.
Smirnov, A.N., Pokrovskaya, E.V., Shevshenko, V.P., Nagaev, I.Yu., Myasoedov, N.F., Levina, I.S., Kulikova, L.E., and Kamernitzky, A.V., Bioorg. Khim., 2002, vol. 28, pp. 251–257 [Russ. J. Bioorg. Chem. (Engl. Transl.), 2002, vol. 28, pp. 224–230].
Levina, I.S., Pokrovskaya, E.V., Kulikova, L.E., Kamernitzky, A.V., Kachala, V.V., and Smirnov, A.N., Steroids, 2008, vol. 73, pp. 815–827.
Shevchenko, V.P., Nagaev, I.Yu., Potapova, A.V., Myasoedov, N.F., Kamernitsky, A.V., Levina, I.S., Kulikova, L.E., and Smirnov, A.N., J. Label. Comp. Radiopharm, 1998, vol. 41, pp. 919–925.
Makkvillin, F. J., Gomogennoe gidrirovanie v organicheskoi khimii (Homogeneous Hydration in Organic Chemistry), Moscow: Khimiya, 1980.
Shevchenko, V.P., Nagaev, I.Yu., and Myasoedov, N.F., Mechennye tritiem lipofil’nye soedineniya (Tritium-Labeled Lipophylic Compounds), Moscow: Nauka, 2003.
Shevchenko, V.P., Nagaev, I.Yu., Bezuglov, V.V., and Myasoedov, N.F., Radiokhimiya, 1989, vol. 31, pp. 121–125.
Shevchenko, V.P., Nagaev, I.Yu., Myasoedov, N.F., Kamernitskii, A.V., Levina, I.S., and Kulikova, L.E., Radiokhimiya, 2000, vol. 42, pp. 176–179.
Shevchenko, V.P., Nagaev, I.Yu., and Myasoedov, N.F., Usp. Khim., 1999, vol. 68, pp. 944–966.
Kamernitskii, A.V., Levina, I.S., Kulikova, L.E., Galakhova, T.N., Shevchenko, V.P., Nagaev, I.Yu., Myasoedov, N.F., Smirnov, A.N., Pokrovskaya, E.V., and Shchelkunova, T.A., Izv. Ros. Akad. Nauk, Ser. Khim., 1997, no. 8, pp. 1532–1535.
Khomutov, R.M., Karpeiskii, M.Ya., and Severin, E.S., Izv. AN SSSR. Ser. Khim., 1962, no. 5, pp. 1074–1076.
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Original Russian Text © V.P. Shevchenko, I.Yu. Nagaev, I.S. Levina, L.E. Kulikova, N.F. Myasoedov, A.V. Kamernitzky, 2010, published in Bioorganicheskaya Khimiya, 2010, Vol. 36, No. 2, pp. 283–288.
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Shevchenko, V.P., Nagaev, I.Y., Levina, I.S. et al. The synthesis of O-substituted 3-oximes of 6α -methyl-16α,17α-cyclohexanopregn-4-ene-3,20-diones tritium-labeled in the 1,2-position. Russ J Bioorg Chem 36, 263–268 (2010). https://doi.org/10.1134/S1068162010020172
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DOI: https://doi.org/10.1134/S1068162010020172


