ORTHO-QUINONE FORMATION IN THE BIOCHEMICAL OXIDATION OF THE ANTI-TUMOR DRUG N2-METHYL-9-HYDROXYELLIPTICINIUM ACETATE

被引：48

作者：

BERNADOU, J

MEUNIER, G

PAOLETTI, C

MEUNIER, B

机构：

[1] CNRS,CHIM COORDINAT LAB,F-31400 TOULOUSE,FRANCE

[2] CNRS,PHARMACOL & TOXICOL FONDAMENTALES LAB,F-31400 TOULOUSE,FRANCE

来源：

JOURNAL OF MEDICINAL CHEMISTRY | 1983年 / 26卷 / 04期

关键词：

D O I：

10.1021/jm00358a022

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

引用

页码：574 / 579

页数：6

共 20 条

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[6] CHEMISTRY OF ORTHO BENZOQUINONES .4. ADDITION OF PRIMARY AROMATIC AMINES TO 1,2-BENZOQUINONE
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[7] REDUCTION OF KETO ACIDS AND DIFFERENTIATION BETWEEN ISOMERS BY CHEMICAL IONIZATION MASS-SPECTROMETRY
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[J]. ANALYTICAL CHEMISTRY, 1980, 52 (01) : 49 - 52
[8] SYNTHESIS AND ANTI-TUMOR ACTIVITY OF CYSTEINYL-3,4-DIHYDROXYPHENYLALANINES AND RELATED-COMPOUNDS
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[J]. JOURNAL OF MEDICINAL CHEMISTRY, 1981, 24 (06) : 673 - 677
[9] NEW ANTITUMORAL AGENT - 9-HYDROXYELLIPTICINE - POSSIBILITY OF A RATIONAL DESIGN OF ANTI-CANCEROUS DRUGS IN SERIES OF DNA INTERCALATING DRUGS
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[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (12) : 5078 - 5082
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