1 ofluorocresol purple and intermolecularly in phenolphthalein (18)F-FDG mixtures.

2                       The laxative action of phenolphthalein (5) is believed to result from induction

3                                              Phenolphthalein (a triphenylmethane derivative) has been

4 e near 540 nm) shows the color change due to phenolphthalein absorption.

5                              In our studies, phenolphthalein administered continuously in the feed fo

6                                              Phenolphthalein alone caused an average fecal potassium

7 ed into four distinct classes (fluoresceins, phenolphthaleins, anthraquinones, and naphthylene sulfon

8  found with phenolphthalein, suggesting that phenolphthalein estrogenic activity alone is not respons

9 der way to identify any potential effects of phenolphthalein exposure at this site in humans.

10                                              Phenolphthalein has been shown to have estrogenic and cl

11 y that the multiple biological properties of phenolphthalein, including its ability to form free radi

12 ei in complex with the nonsubstrate analogue phenolphthalein, inhibitors were designed to take advant

13                      These studies show that phenolphthalein is a multisite/multispecies carcinogen.

14 plus resin caused less potassium output than phenolphthalein plus resin.

15                                              Phenolphthalein regimens were associated with a slight r

16 ance of the mixer is characterized by mixing phenolphthalein solution and sodium hydroxide dissolved

17  of carcinogenic activity as that found with phenolphthalein, suggesting that phenolphthalein estroge

18 er treated for 1 week with magnesium citrate-phenolphthalein to produce chronic osmotic-secretory dia

19 robes and intermolecular quenching by mixing phenolphthalein with (18)F-FDG.