Metabolism of Drugs. XXVII. Metabolic Fate of p-Hydroxybenzoic Acid and its Derivatives in Rabbit. (3).
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The ester-type glucuronide of p-hydroxybenzoic acid was isolated as two derivatives from the urine of rabbits receiving p-hydroxybenzoic acid and their structures were established as methyl (p-methoxybenzoyl 2, 3, 4-tri-O-acetyl-β-D-glucopyranosid) uronate and methyl (p-acetoxybenzoyl 2, 3, 4-tri-O-acetyl-β-D-glucopyranosid) uronate. When feeding p-hydroxybenzoic acid to rabbits, similarly as in using the methyl ester, the unchanged acid, p-hydroxyhippuric acid, the ether-type glucuronide, the estertype glucuronide, and p-carboxyphenyl sulfate were excreted as five metabolites in the urine.
収録刊行物
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- CHEMICAL & PHARMACEUTICAL BULLETIN
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CHEMICAL & PHARMACEUTICAL BULLETIN 10 (2), 91-95, 1962
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390001204173996672
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- NII論文ID
- 110003618809
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- NII書誌ID
- AA00602100
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- ISSN
- 13475223
- 00092363
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可