Cytochrome P450 Family 1 Inhibitors and Structure-Activity Relationships

被引:76
作者
Liu, Jiawang [1 ]
Sridhar, Jayalakshmi [1 ]
Foroozesh, Maryam [1 ]
机构
[1] Xavier Univ Louisiana, Dept Chem, New Orleans, LA 70125 USA
关键词
cytochrome P450; enzyme inhibitor; stilbenoids; flavonoids; structure activity relationships; mechanism-based inhibitor; ARYL-HYDROCARBON RECEPTOR; POLYCYCLIC AROMATIC-HYDROCARBONS; MECHANISM-BASED INACTIVATION; POTENT INHIBITION; P450; 1A1; CATALYTIC-ACTIVITY; HEPATIC ETHOXYRESORUFIN; PREVENTING ACTIVATION; METABOLIC-ACTIVATION; SELECTIVE INHIBITOR;
D O I
10.3390/molecules181214470
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
With the widespread use of O-alkoxyresorufin dealkylation assays since the 1990s, thousands of inhibitors of cytochrome P450 family 1 enzymes (P450s 1A1, 1A2, and 1B1) have been identified and studied. Generally, planar polycyclic molecules such as polycyclic aromatic hydrocarbons, stilbenoids, and flavonoids are considered to potentially be effective inhibitors of these enzymes, however, the details of the structure-activity relationships and selectivity of these inhibitors are still ambiguous. In this review, we thoroughly discuss the selectivity of many representative P450 family 1 inhibitors reported in the past 20 years through a meta-analysis.
引用
收藏
页码:14470 / 14495
页数:26
相关论文
共 109 条
  • [71] SELECTIVE SEROTONIN REUPTAKE INHIBITORS AND THEOPHYLLINE METABOLISM IN HUMAN LIVER-MICROSOMES - POTENT INHIBITION BY FLUVOXAMINE
    RASMUSSEN, BB
    MAENPAA, J
    PELKONEN, O
    LOFT, S
    POULSEN, HE
    LYKKESFELDT, J
    BROSEN, K
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1995, 39 (02) : 151 - 159
  • [72] Contributions of Human Enzymes in Carcinogen Metabolism
    Rendic, Slobodan
    Guengerich, F. Peter
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 2012, 25 (07) : 1316 - 1383
  • [73] Resveratrol, a natural aryl hydrocarbon receptor antagonist, protects lung from DNA damage and apoptosis caused by benzo[a]pyrene
    Revel, A
    Raanani, H
    Younglai, E
    Xu, J
    Rogers, I
    Han, R
    Savouret, JF
    Casper, RF
    [J]. JOURNAL OF APPLIED TOXICOLOGY, 2003, 23 (04) : 255 - 261
  • [74] MECHANISM-BASED INACTIVATION OF CYTOCHROME-P450 2B1 BY 2-ETHYNYLNAPHTHALENE - IDENTIFICATION OF AN ACTIVE-SITE PEPTIDE
    ROBERTS, ES
    HOPKINS, NE
    ALWORTH, WL
    HOLLENBERG, PF
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1993, 6 (04) : 470 - 479
  • [75] Adaptations for the oxidation of polycyclic aromatic hydrocarbons exhibited by the structure of human P450 1A2
    Sansen, Stefaan
    Yano, Jason K.
    Reynald, Rosamund L.
    Schoch, Guillaume A.
    Griffin, Keith J.
    Stout, C. David
    Johnson, Eric F.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (19) : 14348 - 14355
  • [76] FURAFYLLINE IS A POTENT AND SELECTIVE INHIBITOR OF CYTOCHROME-P450IA2 IN MAN
    SESARDIC, D
    BOOBIS, AR
    MURRAY, BP
    MURRAY, S
    SEGURA, J
    DELATORRE, R
    DAVIES, DS
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1990, 29 (06) : 651 - 663
  • [77] Selectivity of polycyclic inhibitors for human cytochrome P450s 1A1, 1A2, and 1B1
    Shimada, T
    Yamazaki, H
    Foroozesh, M
    Hopkins, NE
    Alworth, WL
    Guengerich, FP
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1998, 11 (09) : 1048 - 1056
  • [78] Tissue-specific induction of cytochromes P450 1A1 and 1B1 by polycyclic aromatic hydrocarbons and polychlorinated biphenyls in engineered C57BL/6J mice of arylhydrocarbon receptor gene
    Shimada, T
    Sugie, A
    Shindo, M
    Nakajima, T
    Azuma, E
    Hashimoto, M
    Inoue, K
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 2003, 187 (01) : 1 - 10
  • [79] Different mechanisms for inhibition of human cytochromes P450 1A1, 1A2, and 1B1 by polycyclic aromatic inhibitors
    Shimada, Tsutomu
    Murayama, Norie
    Okada, Kazushi
    Funae, Yoshihiko
    Yamazaki, Hiroshi
    Guengerich, F. Peter
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 2007, 20 (03) : 489 - 496
  • [80] Structure-Function Relationships of Inhibition of Human Cytochromes P450 1A1, 1A2, 1B1, 2C9, and 3A4 by 33 Flavonoid Derivatives
    Shimada, Tsutomu
    Tanaka, Katsuhiro
    Takenaka, Shigeo
    Murayama, Norie
    Martin, Martha V.
    Foroozesh, Maryam K.
    Yamazaki, Hiroshi
    Guengerich, F. Peter
    Komori, Masayuki
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 2010, 23 (12) : 1921 - 1935