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History of Bacterial Chemotherapy
Nomenclature Classification and Synthesis of Sulfanilamide
Activity of Sulfathiazole and Sulfadiarine against
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2-aminopyridine 2-aminothiazole absorption acetylsulfanilyl chloride acid Activities References CH activity in vivo acyl alkyl American Chemical Society amide amine amino anilamide appear aqueous bacterial bacteriostatic blood levels carbonate CH,O CH.CONH CH.O Chapter chemotherapeutic agents chemotherapy CHOH clinical coli compounds concentration condensed Derivatives of Sulfanilamide Derivatives Table dyes effect ences excreted guanidine Heterocyclic Heterocyclic System HOOC HOOCCH hydrolysis hydrolyzed inactive infections isomeric large number literature melting form Melting Range Activities methyl mice Miscellaneous monograph N-Atoms nitro nitrogen Nuclear-substituted p-aminobenzenesulfonamide PABA patent Pharmacology pneumococci Prontosil pyridine R1 Melting Range Range Activities References Ri Ri ring Salts of Sulfanilamide showed SO,N SO,NH SO.NH sodium hydroxide sodium salt soluble solution streptococci structure studied substituted sulfanilamides sulfa drugs sulfadiazine sulfaguanidine sulfamethazine sulfanilamide derivatives Sulfanilamides Table sulfanilic sulfapyridine sulfathiazole sulfonamide sulfonamide drugs sulfones sulfonyl sulfonyl chloride Synthesis tested therapeutic tion treatment vitro vivo activity