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Letters to Nature
Nature 177, 478 - 479 (10 March 1956); doi:10.1038/177478b0

Comparative Antio eligstrogenic Potencies of Progesterone and 17alpha-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 antistrogenic actions: it prevents strogen-induced abdominal fibroids, strogen-induced growth of the myometrium, and strogen-induced excessive luteinization1. The antistrogenic 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 11beta-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 17alpha-OH-11-deoxycorticosterone2. Thus the conclusion as to loss of antistrogenic potencies due to oxidation at C17 in the alpha-position has been so far an indirect one; a comparison of progesterone with 17alpha-hydroxyprogesterone was still lacking. Results with the latter are given in the present communication.

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  2. Mardones, E. , Iglesias, R. and Lipschutz, A. , Nature, 174, 839 (1954). | Article | PubMed | ISI | ChemPort |
  3. Mardones, E. , Iglesias, R. , and Lipschutz, A. , Endocrin. (in the press).
  4. Mardones, E. , Iglesias, R. , and Lipschutz, A. , Experientia, 9, 303 (1953). | Article | PubMed | ISI | ChemPort |
  5. 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 |
  6. 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 |



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