INHIBITOR PROPERTIES OF SOME 5-SUBSTITUTED URACIL ACYCLONUCLEOSIDES, AND 2,2'-ANHYDROURIDINES VERSUS URIDINE PHOSPHORYLASE FROM ESCHERICHIA-COLI AND MAMMALIAN SOURCES

被引：18

作者：

DRABIKOWSKA, AK ^{[1
]}

LISSOWSKA, L ^{[1
]}

VERES, Z ^{[1
]}

SHUGAR, D ^{[1
]}

机构：

[1] HUNGARIAN ACAD SCI,CENT RES INST CHEM,H-1525 BUDAPEST,HUNGARY

来源：

BIOCHEMICAL PHARMACOLOGY | 1987年 / 36卷 / 23期

关键词：

D O I：

10.1016/0006-2952(87)90570-3

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

页码：4125 / 4128

页数：4

共 13 条

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[6] SYNTHESIS OF 1-[[2-HYDROXY-1-(HYDROXYMETHYL)ETHOXY]METHYL]-5-BENZYLURACIL AND ITS AMINO ANALOG, NEW POTENT URIDINE PHOSPHORYLASE INHIBITORS WITH HIGH WATER SOLUBILITY [J].

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[8] PYRIMIDINE ACYCLONUCLEOSIDES, INHIBITORS OF URIDINE PHOSPHORYLASE [J].

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ELKOUNI, MH ;

CHU, SH ;

CHA, S .

BIOCHEMICAL PHARMACOLOGY, 1981, 30 (15) :2097-2101

[9] 5-BENZYLACYCLOURIDINE AND 5-BENZYLOXYBENZYLACYCLOURIDINE, POTENT INHIBITORS OF URIDINE PHOSPHORYLASE [J].

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