Inhibitors of NADH-ubiquinone reductase: an overview

被引:431
作者
Esposti, MD [1 ]
机构
[1] Monash Univ, Dept Biochem & Mol Biol, Clayton, Vic 3168, Australia
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 1998年 / 1364卷 / 02期
关键词
NADH-ubiquinone reductase; respiratory inhibitor; ubiquinone;
D O I
10.1016/S0005-2728(98)00029-2
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
This article provides an updated overview of the plethora of complex I inhibitors. The inhibitors are presented within the broad categories of natural and commercial compounds and their potency is related to that of rotenone, the classical inhibitor of complex I. Among commercial products, particular attention is dedicated to inhibitors of pharmacological or toxicological relevance. The compounds that inhibit the NADH-ubiquinone reductase activity of complex I are classified according to three fundamental types of action on the basis of available evidence and recent insights: type A are antagonists of the ubiquinone substrate, type B displace the ubisemiquinone intermediate, and type C are antagonists of the ubiquinol product. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:222 / 235
页数:14
相关论文
共 144 条
  • [1] MODE OF ACTION OF BULLATACIN - A POTENT ANTITUMOR AND PESTICIDAL ANNONACEOUS ACETOGENIN
    AHAMMADSAHIB, KI
    HOLLINGWORTH, RM
    MCGOVREN, JP
    HUI, YH
    MCLAUGHLIN, JL
    [J]. LIFE SCIENCES, 1993, 53 (14) : 1113 - 1120
  • [2] THE NON-EQUIVALENCE OF BINDING-SITES OF COENZYME QUINONE AND ROTENONE IN MITOCHONDRIAL NADH-COQ REDUCTASE
    AHMED, I
    KRISHNAMOORTHY, G
    [J]. FEBS LETTERS, 1992, 300 (03) : 275 - 278
  • [3] ANOMALOUS RESPONSE OF OXONOL-V TO MEMBRANE-POTENTIAL IN MITOCHONDRIAL PROTON PUMPS
    AHMED, I
    KRISHNAMOORTHY, G
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1994, 1188 (1-2): : 131 - 138
  • [4] MITOCHONDRIAL RESPIRATORY INHIBITION BY N-METHYLATED BETA-CARBOLINE DERIVATIVES STRUCTURALLY RESEMBLING N-METHYL-4-PHENYLPYRIDINE
    ALBORES, R
    NEAFSEY, EJ
    DRUCKER, G
    FIELDS, JZ
    COLLINS, MA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (23) : 9368 - 9372
  • [5] ANDERSON WM, 1995, BBA-BIOENERGETICS, V1230, P186
  • [6] INHIBITION OF MITOCHONDRIAL AND PARACOCCUS-DENITRIFICANS NADH UBIQUINONE REDUCTASE BY OXACARBOCYANINE DYES - A STRUCTURE-ACTIVITY STUDY
    ANDERSON, WM
    WOOD, JM
    ANDERSON, AC
    [J]. BIOCHEMICAL PHARMACOLOGY, 1993, 45 (10) : 2115 - 2122
  • [7] ANDERSON WM, 1989, BIOCHEM INT, V19, P673
  • [8] ANDERSON WM, 1993, BIOCHEM PHARMACOL, V45, P91
  • [9] 3-(2-THIENYLVINYL)INDOLES AS POTENTIAL SPECIFIC INHIBITORS OF THE ENERGY-METABOLISM IN HELMINTHIC PARASITES
    ANDREANI, A
    RAMBALDI, M
    LOCATELLI, A
    ANDREANI, F
    POGLAYEN, G
    DEGLIESPOSTI, M
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1992, 27 (07) : 729 - 734
  • [10] THIENYLIMIDAZO[2,1-B]THIAZOLES AS INHIBITORS OF MITOCHONDRIAL NADH DEHYDROGENASE
    ANDREANI, A
    RAMBALDI, M
    LEONI, A
    LOCATELLI, A
    GHELLI, A
    RATTA, M
    BENELLI, B
    ESPOSTI, MD
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (07) : 1090 - 1097