Journal of labelled compounds and radiopharmaceuticals p. 1199 - 1203 (1995)
Update date:2022-08-04
Topics:
Mais
Chen
Wagoner
Scott Hayes
Wang
[3H]RU38486 (RU486) was synthesized from its penultimate precursor, desmethyl RU486, by substitution of the secondary amine with tritiated methyl iodide; specific activity 85 Ci/mmol. Ligand binding studies confirm that RU486 binds with high affinity to human progesterone receptor type A (PR-A) and progesterone receptor type B (PR-B).
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