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J Med Chem ; 20(4): 591-4, 1977 Apr.
Article in English | MEDLINE | ID: mdl-850246

ABSTRACT

A series of 27 hydantoins was prepared and tested as antitumor agents. These were variously substituted in the 5 position but with special emphasis on the substituents (chloro, acetyl, chloroacetyl, and methyl) in the 1 and/or 3 positions. The most active compound was 5,5-bis(4-chlorophenyl)-1,3-dichlorohydantoin with a T/C value of 190% against P-388 lymphocytic leukemia in mice.


Subject(s)
Antineoplastic Agents/chemical synthesis , Hydantoins/chemical synthesis , Animals , Antineoplastic Agents/therapeutic use , Hydantoins/pharmacology , Hydantoins/therapeutic use , Leukemia L1210/drug therapy , Leukemia, Experimental/drug therapy , Methods , Mice
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