1 ug-albumin adduct by a competitive compound, sulfanilamide.

2 coupling reaction, and synthesis of the drug sulfanilamide.

3 as induced by blocking folate synthesis with sulfanilamide.

4  were sulfanilic acid and 3A5MI, followed by sulfanilamide and (5-methylisoxazol-3-yl)-sulfamate, whe

5 h colorimetric detection technique employing sulfanilamide and N-(1-naphthyl)ethylenediamine dihydroc

6  among structurally similar molecules, i.e., sulfanilamide and sulfadimethoxine.

7 totype inhibitors N4-(6-aminopyrimidin-4-yl)-sulfanilamide (APS) and 1-(5-cyclobutyl-thiazol-2-yl)-3-

8 isca Inc) to generate calibration curves and sulfanilamide as an internal standard.

9 umin, and hemoglobin are stable in acidified sulfanilamide as determined by the tri-iodide method, co

10 agent conferring resistance to streptomycin, sulfanilamide, gentamicin, and carbenicillin in 1975.

11 hiazole-based chalcone derivatives bearing a sulfanilamide moiety as the zinc-binding group for selec

12                         Solutions containing sulfanilamide/N-(1-naphthyl)- ethylenediamine dihydrochl

13 otized aminobenzenes namely sulfanilic acid, sulfanilamide, or aniline with TPCs in the extract to fo

14 The discovery of antibiotics, beginning with sulfanilamide, penicillin, and streptomycin, led to addi

15 m is based on the beliefs that (i) acidified sulfanilamide pretreatment, required to remove nitrite,

16 ated its application to activate nitro-caged sulfanilamide prodrug in formate-abundant bacteria, spec

17 aration of a medicinal product, an elixir of sulfanilamide, resulting in deaths, public outcry hasten

18          Released nitrogen oxide reacts with sulfanilamide (SA) and N-(1-napthyl)ethylenediamine (NNE

19  is also extended to the omega-unsaturated N-sulfanilamide to furnish piperidines.