|
Comparative Anti strogenic Potencies of Progesterone and 17 -Hydroxyprogesterone ELVIRA MARDONES, DUSAN JADRIJEVIC & A. LIPSCHUTZ
Instituto de Medicina Experimental, Servicio Nacional de Salud, Av. Irarrázaval 849, Santiago, Chile. October 15.
PROGESTERONE is known to be not only a progestational compound but also to exert various anti strogenic actions: it prevents strogen-induced abdominal fibroids, strogen-induced growth of the myometrium, and strogen-induced excessive luteinization1. The anti strogenic potency of progesterone is diminished by oxidation at C21, C11 and C17
2,3. The validity of this rule has been demonstrated by comparing progesterone with C11-derivatives such as 11 -hydroxyprogesterone and 11-keto-progesterone, and with a C21-derivative such as deoxycorticosterone. As to oxidation at C17, comparison was made between deoxycorticosterone and Reichstein's compound S or 17 -OH-11-deoxycorticosterone2. Thus the conclusion as to loss of anti strogenic potencies due to oxidation at C17 in the -position has been so far an indirect one; a comparison of progesterone with 17 -hydroxyprogesterone was still lacking. Results with the latter are given in the present communication.
-
Lipschutz, A.
, "Steroid Hormones and Tumors" (Williams and Wilkins Co., Baltimore, 1950).
Mardones, E.
,
Bruzzone, S.
,
Iglesias, R.
, and
Lipschutz, A.
, Endocrin., 49, 817 (1951). | ISI |
-
Mardones, E.
,
Iglesias, R.
and
Lipschutz, A.
, Nature, 174, 839 (1954). | Article | PubMed | ISI | ChemPort |
-
Mardones, E.
,
Iglesias, R.
, and
Lipschutz, A.
, Endocrin. (in the press).
-
Mardones, E.
,
Iglesias, R.
, and
Lipschutz, A.
, Experientia, 9, 303 (1953). | Article | PubMed | ISI | ChemPort |
-
Levy, H.
,
Jeanloz, W.
,
Jacobsen, R. P.
,
Hechter, O.
,
Schenker, V.
and
Pincus, G.
, J. Biol. Chem., 211, 867 (1954).
Brownie, A. C.
Grant, J. K.
, and
Davidson, D. W.
, Biochem. J., 58, 218 (1954). | PubMed | ISI | ChemPort |
-
Junkmann, K.
, Arch. Exp. Path. u. Pharmakol., 223, 244 (1954).,
Davies, M. E.
, and
Wied, G. L.
, J. Clin. Endocrinol. and Metab., 15, 923 (1955). | ChemPort |
© 1956 Nature Publishing Group Privacy Policy |