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J Pharm Sci ; 66(2): 263-4, 1977 Feb.
Article in English | MEDLINE | ID: mdl-839425

ABSTRACT

Several derivatives of 2-indolyl 5-(1,2,3,6-tetrahydropyridyl) ketone with various substituents on the pyridine nitrogen and with or without a benzenesulfonyl group on the indole nitrogen were synthesized and characterized by spectroscopic and analytical data. Only one showed erratic but confirmed activity in the P-388 screen. The other derivatives were inactive in the L-1210 leukemia screen.


Subject(s)
Antineoplastic Agents/chemical synthesis , Indoles/chemical synthesis , Alkylation , Animals , Antineoplastic Agents/therapeutic use , Cell Survival/drug effects , Cells, Cultured , Indoles/pharmacology , Leukemia L1210/drug therapy , Leukemia, Experimental/drug therapy , Mice , Oxidation-Reduction , Pyridines/chemical synthesis , Pyridines/pharmacology
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