Syntheses of Catechol Estrogen 16,17-Ketols, New and Potential Metabolites
スポンサーリンク
概要
- 論文の詳細を見る
In order to characterize the biliary metabolites the catechol estrogen 16,17-ketols and their monomethyl ethers have been synthesized as reference compounds employing the method worked out by Gallagher and his co-workers. The preparation of 2-methoxy-16α-hydroxyestrone 3-glucuronide acetate-methyl ester (Vd) has also been described.
- 公益社団法人日本薬学会の論文
- 1973-12-25
著者
-
本間 誠次郎
Pharmaceutical Institute Tohoku University
-
本間 誠次郎
Research Division, Teikoku Hormone Mfg. Co.
-
野久保 宗孝
Pharmaceutical Institute, Tohoku University
-
川原田 良彦
Pharmaceutical Institute Tohoku University
-
野久保 宗孝
First Laboratory Of Clinical Physiology
関連論文
- Mass Spectral Rearrangement : A Scope of Rearrangement of Alkylaminomethyl Group to the Ring in 1-Alkylamino-3-aryloxy-2-propanol Derivatives
- Studies on Steroid Conjugates. IX. New Synthesis of Estriol 16-and 17-Monoglucuronides
- Studies on Steroid Conjugates. XII. Occurrence of 16-Epiestriol 16-Glucuronide in Human Pregnancy Urine
- Studies on Steroid Conjugates. V. Synthesis of 16-Epiestriol 3-Glucuronide
- Studies on Steroid Conjugates. XIV. Participation of Glucuronidation in Selective O-Methylation of Catechol Estrogen in the Rat
- Evidence for O-Methylation of Catechol Estrogen 2-Glucuronoside with Retention of Conjugate in the Rat
- Isolation and Characterization of Biliary Metabolites of Estrone in the Rat
- Syntheses of Catechol Estrogen 16,17-Ketols, New and Potential Metabolites
- Isomeric 2,16α-Dihydroxyestrone Methyl Ethers : New Metabolites in Rat Bile
- Studies on Steroid Conjugates. X. Significance of Conjugation involved in Biosynthesis of 2-Methoxyestrogen
- 2-Methoxyestrone 3-Glucuronide : A New Biliary Metabolite in the Rat
- C-2 Hydroxylation of 2-Deuterioestrogen in the Rat. Lack of "NIH Shift"
- Studies on Steroid Conjugates. IV. Synthesis of Catechol Estrogen Monoglucuronides
- Studies on Steroid Conjugates. III. New Syntheses of 2-Methoxyestrogens
- Stereoselectivity in the Metabolism of the β-Adrenergic Blocking Agent, (±)-1-tert-Butylamino-3-(2,3-dimethylphenoxy)-2-propanol Hydrochloride (Xibenolol Hydrochloride, D-32), in Man
- Isolation and Characterization of Metabolites derived from 1-tert-Butylamino-3-(2,3-dimethylphenoxy)-2-propanol (D-32), a New β-Blocker
- Syntheses of 16,17-Dihydroxy-17-methyl-5α-androstano [3,2-c] isoxazoles
- The Effects of Phenobarbital, Spironolactone and Diazepam on Hepatic 3-Hydroxy-3-methylglutaryl Coenzyme A Reductase Activity in Male and Female Rats
- Isolation and Characterization of Biliary Metabolites of Estriol in the Rat
- ステロイドの分析化学的研究(第61報)ステロイド系脱コレステロール剤ヒト尿中代謝産物のガスクロマトグラフィー
- Biliary Conjugated Metabolites of Estriol in the Rat
- Syntheses of Methoxyestrogen Glucuronide Acetate-Methyl Esters
- Syntheses of 16β-Oxygenated Catechol Estrogen Methyl Ethers, New and Potential Metabolites
- Conjugated Metabolites of Estriol in Rat Bile
- In Vitro Reduction of 16α-Chloroestrone by Rat Liver
- Syntheses of Epimeric 2-Hydroxy-16-chloroestrone Monomethyl Ethers
- Epimerization of Halogen during in Vivo Transformation of 16α-Chloroestrone Methyl Ether