论文信息 - Inhibitors of human placental C19 and C21 3β-hydroxysteroid dehydrogenases - 字舞流文

Inhibitors of human placental C19 and C21 3β-hydroxysteroid dehydrogenases

A. Goldman | K. Sheth

[1] J. C. Warren,et al. Synthesis of 2 -, 6 -, and 6 -bromoprogesterone and study of the binding site of 20 -hydroxysteroid dehydrogenase. , 1972, Biochemistry.

[2] R. E. Oakey,et al. The role of 3 -hydroxysteroid dehydrogenase-isomerase in the conversion of dehydroepiandrosterone to estrogens by a preparation of human placental microsomes in vitro. , 1972, Steroids.

[3] P. Talalay,et al. An active-site-directed irreversible inhibitor of 5 -3-ketosteroid isomerase. , 1971, Biochimica et biophysica acta.

[4] E. Bloch,et al. Studies on the inhibition of fetal androgen formation. Inhibition of testosterone synthesis in rat and rabbit fetal testes with observations on reproductive tract development. , 1971, Endocrinology.

[5] A. Goldman. Specific retention of an inhibitor of 3-beta-hydroxysteroid dehydrogenase in enzyme-containing tissues of the rat. , 1970, Endocrinology.

[6] A. Goldman. Maternal and Fetal Effects of Two Inhibitors of 3β-Hydroxysteroid Dehydrogenase and Δ5–4,3-Ketosteroid Isomerase in the Rat , 1969 .

[7] A. Neville,et al. Inhibition of - and -Hydroxysteroid Dehydrogenases and Steroid -Isomerase by Substrate Analogues , 1968 .

[8] A. Burger. Design of Active-Site-Directed Irreversible Enzyme Inhibitors. , 1967 .