Substituted Amides and Hydrazides of Dicarboxylic Acids. Part 15. Synthesis and Hypoglycemic Activity of Some Amides and Acylhydrazides of Tetrachlorophthalic Acid

Pharmaceutical Chemistry Journal -     

Substituted Amides and Hydrazides of Dicarboxylic Acids. Part 10. Synthesis and Pharmacological Activity of Substituted Amides and Hydrazides of Succinic Acid

Pharmaceutical Chemistry Journal -     

Substituted Amides and Hydrazides of Dicarboxylic Acids. Part 13. Synthesis and Hypoglycemic Activity of Some Substituted Amides and Acylhydrazides of Phthalic Acid

Pharmaceutical Chemistry Journal -     

Substituted Amides and Hydrazides of Dicarboxylic Acids. Part 17. Synthesis and Antibacterial and Anticonvulsant Activity of Some Amides and Acylhydrazides of Phthalic Acid

Pharmaceutical Chemistry Journal -     

Amides of polyene macrolide aureofacin. Synthesis and biological properties

Synthesis and biological properties of a number of amides of polyene macrolide antibiotic aureofacin obtained in the reaction of the antibiotic with various glycine esters are described.     

Synthesis and antiarrhythmic and parasympatholytic properties of substituted phenols. 2. Amides

Thirty amides patterned after the antiarrhythmic drug changrolin were synthesized and their antiarrhythmic and parasympatholytic activities were assessed. There was no correlation between antiarrhythmic and parasympatholytic activities. Several of the amides were found to be potent antiarrhythmic agents that possessed low parasympatholytic activity. All of the compounds appear to act by a class I mechanism.     

Substituted Amides and Hydrazides of Acylpyruvic Acids. Part 9. Synthesis,Antimicrobial and Analgesic Activity of Substituted 4-Aryl-3-halogen-2,4-dioxobutanoic Acid Amides

Pharmaceutical Chemistry Journal -     

Amides and hydrazides of oxalic acid XVI. Basic amides of alkoxyoxanilic acids

Conclusions Some basic amides of alkoxyoxanilic acids, their salts and their quaternary halide salts have been synthesized; and their properties and biological activity have been studied.Translated from Khimiko-Farmatsevticheskii Zhurnal, No. 12, pp, 7–12, December, 1967.