ANTHRAFLAVIC ACID IS A POTENT AND SPECIFIC INHIBITOR OF CYTOCHROME-P-448 ACTIVITY

被引：15

作者：

AYRTON, AD ^{[1
]}

LEWIS, DFV ^{[1
]}

IOANNIDES, C ^{[1
]}

WALKER, R ^{[1
]}

机构：

[1] UNIV SURREY,DEPT BIOCHEM,GUILDFORD GU2 5XH,SURREY,ENGLAND

来源：

BIOCHIMICA ET BIOPHYSICA ACTA | 1987年 / 916卷 / 03期

关键词：

D O I：

10.1016/0167-4838(87)90177-4

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

收藏

页码：328 / 331

页数：4

相关论文

共 18 条

[1] BURKE MD, 1983, CHEM-BIOL INTERACT, V45, P243
[2] BURKE MD, 1974, DRUG METAB DISPOS, V2, P583
[3] INHIBITION OF CYTOCHROME P-448 MIXED-FUNCTION OXIDASE ACTIVITY FOLLOWING ADMINISTRATION OF 9-HYDROXYELLIPTICINE TO RATS
DELAFORGE, M
IOANNIDES, C
PARKE, DV
[J]. CHEMICO-BIOLOGICAL INTERACTIONS, 1980, 32 (1-2) : 101 - 110
[4] PURIFICATION AND CHARACTERIZATION OF MICROSOMAL CYTOCHROME-P-450S
GUENGERICH, FP
DANNAN, GA
WRIGHT, ST
MARTIN, MV
KAMINSKY, LS
[J]. XENOBIOTICA, 1982, 12 (11) : 701 - 716
[5] MECHANISM OF INDUCTION OF HEPATIC MICROSOMAL DRUG-METABOLIZING ENZYMES BY A SERIES OF BARBITURATES
IOANNIDES, C
PARKE, DV
[J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 1975, 27 (10) : 739 - 746
[6] CYTOCHROME-P-448 AND THE ACTIVATION OF TOXIC-CHEMICALS AND CARCINOGENS
IOANNIDES, C
LUM, PY
PARKE, DV
[J]. XENOBIOTICA, 1984, 14 (1-2) : 119 - 137
[7] IOANNIDES C, 1987, IN PRESS BIOCH PHARM
[8] N-HYDROXYLATION OF CARCINOGENIC AND MUTAGENIC AROMATIC-AMINES
KATO, R
KAMATAKI, T
YAMAZOE, Y
[J]. ENVIRONMENTAL HEALTH PERSPECTIVES, 1983, 49 (MAR) : 21 - 25
[9] ELLIPTICINES AS POTENT INHIBITORS OF ARYL-HYDROCARBON HYDROXYLASE - THEIR BINDING TO MICROSOMAL CYTOCHROMES P450 AND PROTECTIVE EFFECT AGAINST BENZO(A)PYRENE MUTAGENICITY
LESCA, P
LECOINTE, P
PAOLETTI, C
MANSUY, D
[J]. BIOCHEMICAL PHARMACOLOGY, 1978, 27 (08) : 1203 - 1209
[10] MOLECULAR DIMENSIONS OF THE SUBSTRATE BINDING-SITE OF CYTOCHROME-P-448
LEWIS, DFV
IOANNIDES, C
PARKE, DV
[J]. BIOCHEMICAL PHARMACOLOGY, 1986, 35 (13) : 2179 - 2185