| Identification | More | [Name]
Inabenfide | [CAS]
82211-24-3 | [Synonyms]
INABENFIDE
SERITARD
4’-chloro-2’-(alpha-hydroxybenzyl)isonicotinanilide
cgr-811
n-(4-chloro-2-(hydroxyphenylmethyl)phenyl)-4-pyridinecarboxamid
n-(4-chloro-2-(hydroxyphenylmethyl)phenyl)-4-pyridinecarboxamide
4′-Chloro-2′-(α-hydroxybenzyl)isonicotinanilide
N-[4-Chloro-2-(hydroxy-phenylmethyl)phenyl]pyridine-4-carboxamide
N-[4-Chloro-2-(α-hydroxybenzyl)phenyl]isonicotinamide | [Molecular Formula]
C19H15ClN2O2 | [MDL Number]
MFCD00210319 | [Molecular Weight]
338.79 | [MOL File]
82211-24-3.mol |
| Hazard Information | Back Directory | [Definition]
ChEBI:Inabenfide is a diarylmethane. | [Metabolic pathway]
In rats, inabenfide is mainly hydroxylated on the
phenyl ring which is not substituted by a chlorine atom
through epoxidation. Oxidation of the benzyl alcohol
gives benzophenone. The other hydroxylation is the
substitution of the chlorine with hydroxyl of the other phenyl ring possessing a chlorine atom. Also,
hydrolysis of the amide bond resulting in the
corresponding aniline and N-oxidation of the pyridine
nitrogen can be observed. |
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