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7 ed into four distinct classes (fluoresceins, phenolphthaleins, anthraquinones, and naphthylene sulfon
9 found with phenolphthalein, suggesting that phenolphthalein estrogenic activity alone is not respons
12 y that the multiple biological properties of phenolphthalein, including its ability to form free radi
13 ei in complex with the nonsubstrate analogue phenolphthalein, inhibitors were designed to take advant
17 ance of the mixer is characterized by mixing phenolphthalein solution and sodium hydroxide dissolved
18 of carcinogenic activity as that found with phenolphthalein, suggesting that phenolphthalein estroge
19 er treated for 1 week with magnesium citrate-phenolphthalein to produce chronic osmotic-secretory dia
20 s based on methyl red, bromothymol blue, and phenolphthalein, which responded to a pH range from 5.0