STRUCTURE-ACTIVITY RELATIONSHIPS IN POLYCYCLIC AROMATIC-HYDROCARBONS - INDUCTION OF MICROSOMAL ARYL HYDROCARBON HYDROXYLASE AND ITS POSSIBLE IMPORTANCE IN CHEMICAL CARCINOGENESIS

被引：28

作者：

FRANKE, R ^{[1
]}

机构：

[1] GERMAN ACAD SCI,RES CTR MOLEC BIOL & MED,CENT INST MOLEC BIOL,DEPT DRUG RES,BERLIN,EAST GERMANY

来源：

CHEMICO-BIOLOGICAL INTERACTIONS | 1973年 / 6卷 / 01期

关键词：

D O I：

10.1016/0009-2797(73)90081-1

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

页码：1 / 17

页数：17

共 32 条

[21] IMMUNOSUPPRESSION BY POLYCYCLIC AROMATIC-HYDROCARBONS - A STRUCTURE-ACTIVITY RELATIONSHIP IN B6C3F1 AND DBA/2 MICE
WHITE, KL
LYSY, HH
HOLSAPPLE, MP
IMMUNOPHARMACOLOGY, 1985, 9 (03): : 155 - 164
[22] QUANTITATIVE STRUCTURE ACTIVITY RELATIONSHIPS FOR POLYCYCLIC AROMATIC-HYDROCARBONS - CORRELATION BETWEEN MOLECULAR CONNECTIVITY, PHYSICOCHEMICAL PROPERTIES, BIOCONCENTRATION AND TOXICITY IN DAPHNIA-PULEX
GOVERS, H
RUEPERT, C
AIKING, H
CHEMOSPHERE, 1984, 13 (02) : 227 - 236
[23] Vertex indices of molecular graphs in structure-activity relationships. A study of the convulsant-anticonvulsant activity of barbiturates and the carcinogenicity of unsubstituted polycyclic aromatic hydrocarbons
Klopman, G
Raychaudhury, C
1600, (30):
[24] ARYL-HYDROCARBON HYDROXYLASE INDUCTION IN ADULT-RAT HEPATOCYTES IN PRIMARY CULTURE BY SEVERAL CHLORINATED AROMATIC-HYDROCARBONS INCLUDING 2,3,7,8-TETRACHLORODIBENZO-PARA-DIOXIN
JANSING, RL
SHAIN, W
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1985, 5 (04): : 713 - 720
[25] Crystal Structures of trans-Tetrahydrotetrols of Benzo[a]pyrene and Chrysene: A Possible Structure-Activity Relationship in Quasi-Planar Bay-Region Polycyclic Aromatic Hydrocarbons
Fiorella Bachechi
Chiara Polcaro
Structural Chemistry, 1999, 10 : 135 - 148
[26] Crystal structures of trans-tetrahydrotetrols of benzo[a]pyrene and chrysene:: A possible structure-activity relationship in quasi-planar bay-region polycyclic aromatic hydrocarbons
Bachechi, F
Polcaro, C
STRUCTURAL CHEMISTRY, 1999, 10 (02) : 135 - 148
[27] AH RECEPTOR IN MICE GENETICALLY NONRESPONSIVE FOR CYTOCHROME-P4501A1 INDUCTION - CYTOSOLIC AH RECEPTOR, TRANSFORMATION TO THE NUCLEAR-BINDING STATE, AND INDUCTION OF ARYL-HYDROCARBON HYDROXYLASE BY HALOGENATED AND NONHALOGENATED AROMATIC-HYDROCARBONS IN EMBRYONIC-TISSUES AND CELLS
HARPER, PA
GOLAS, CL
OKEY, AB
MOLECULAR PHARMACOLOGY, 1991, 40 (05) : 818 - 826
[28] Mechanistic quantitative structure-activity relationship model for the photoinduced toxicity of polycyclic aromatic hydrocarbons .1. Physical model based on chemical kinetics in a two-compartment system
Krylov, SN
Huang, XD
Zeiler, LF
Dixon, DG
Greenberg, BM
ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY, 1997, 16 (11) : 2283 - 2295
[29] OOCYTE DESTRUCTION BY POLYCYCLIC AROMATIC-HYDROCARBONS IS NOT LINKED TO THE INDUCIBILITY OF OVARIAN ARYL-HYDROCARBON (BENZO(A)PYRENE) HYDROXYLASE-ACTIVITY IN (DBA/2N X C57BL/6N) F1 X DBA/2N BACKCROSS MICE
MATTISON, DR
NIGHTINGALE, MS
PEDIATRIC PHARMACOLOGY, 1982, 2 (01): : 11 - 21
[30] EFFECTS OF SUBSTITUENTS ON THE CYTOSOLIC RECEPTOR-BINDING AVIDITIES AND ARYL-HYDROCARBON HYDROXYLASE INDUCTION POTENCIES OF 7-SUBSTITUTED 2,3-DICHLORODIBENZO-PARA-DIOXINS - A QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP ANALYSIS
DENOMME, MA
HOMONOKO, K
FUJITA, T
SAWYER, T
SAFE, S
MOLECULAR PHARMACOLOGY, 1985, 27 (06) : 656 - 661

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