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Journal of Pharmacology And Experimental Therapeutics, Vol. 115, Issue 4, 408-412, 1955
Copyright © 1955 by American Society for Pharmacology and Experimental Therapeutics


OBSERVATIONS ON THE RELATION OF CHEMICAL STRUCTURE TO THE PRODUCTION OF ADRENAL CORTICAL ATROPHY OR HYPERTROPHY IN THE DOG BY DERIVATIVES OF 2,2-BIS-(p-CHLOROPHENYL)-1,1-DICHLOROETHANE (DDD, TDE)

P. S. Larson 1, Gordon R. Hennigar 1, J. K. Finnegan 1, R. Blackwell Smith Jr. 1, and H. B. Haag 1

1 Departments of Pharmacology and Pathology, Medical College of Virginia, Richmond, Virginia

A biochemorphologic study of the compound 2,2-bis-(p-chlorophenyl)-1,1-dichloroethane in relation to its ability to produce adrenal cortical atrophy in the dog has shown the following: Both phenyl groups in the molecule are necessary for the production of atrophy, but the paraphenyl substitutions are not. Any change in the number of chlorine substitutions (0, 1 or 3) on the ethane portion of the molecule, substitution of —OH for the —H in the 2-position or desaturation to the ethylene analogue abolishes the ability to produce adrenal cortical atrophy. The latter two compounds gave evidence of production of adrenal cortical hypertrophy and 1,1-p-chlorophenyl ethane produced hyperplasia. In the case of one of the derivatives studied, 2,2-bis(p-ethyl-phenyl)1,1-dichboroethane, it was further shown that administration of cortisone offers some protection against the lethal consequence of the adrenal cortical atrophy produced.

Submitted on July 11, 1955







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Copyright © 1955 by the American Society for Pharmacology and Experimental Therapeutics.