Metabolism of 5 : 5-Diphenylhydantoin in the Rabbit
BUTLER 1 has shown that the metabolism of 5 : 5-diphenylhydantoin in man leads to the excretion of what is presumed to be the pure lævorotatory form of 5-( p -hydroxyphenyl)-5-phenylhydantoin, melting point 326–328° (decomp.), [α] 28 D − 16° ( c . 0.4 in ethanol), through hydroxylation in one ring o...
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Veröffentlicht in: | Nature (London) 1957-06, Vol.179 (4572), p.1248-1248 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | BUTLER
1
has shown that the metabolism of 5 : 5-diphenylhydantoin in man leads to the excretion of what is presumed to be the pure lævorotatory form of 5-(
p
-hydroxyphenyl)-5-phenylhydantoin, melting point 326–328° (decomp.), [α]
28
D
− 16° (
c
. 0.4 in ethanol), through hydroxylation in one ring only. In dogs, however, hydroxylation of either of the two phenyl groups appears to proceed with almost equal facility: the excreted
p
-hydroxy derivative is slightly dextrorotatory. |
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ISSN: | 0028-0836 1476-4687 |
DOI: | 10.1038/1791248a0 |