Quinoids, quinoid radicals, and phenoxyl radicals formed from estrogens and antiestrogens

被引:98
|
作者
Bolton, JL [1 ]
机构
[1] Univ Illinois, Coll Pharm, Dept Med Chem & Pharmacognosy, Chicago, IL 60612 USA
关键词
estrogen; antiestrogen; catechol; o-quinone; semiquinone radical; phenoxyl radical;
D O I
10.1016/S0300-483X(02)00195-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Estrogens have a variety of beneficial effects in vivo including protection against osteoporosis, coronary heart disease, Alzheimer's disease, and stroke. Similarly, antiestrogens have been shown to be effective both in treating breast cancer as well as preventing this disease. Despite the health benefits of these drugs adverse side effects have been reported including increased risk for developing certain hormone dependent cancers. Although an estrogenic mechanism likely contributes to mechanism of estrogen/antiestrogen carcinogenesis there is substantial evidence to suggest that metabolism to reactive intermediates is also involved. Both estrogens and antiestrogens can be metabolized to phenoxyl radicals, o-quinones, and semiquinone radicals, all of which could cause damage in cells either through alkylation or oxidation of cellular macromolecules including DNA. In contrast, there are several reports that estrogens and antiestrogens can act as antioxidants which could protect cells against free radical mediated damage and contribute to the beneficial effects of these compounds discussed above. The focus of this review is the role of quinoids, quinoid radicals, and phenoxyl radicals in the biological effects of estrogens and antiestrogens. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:55 / 65
页数:11
相关论文
共 50 条
  • [41] DEHYDRATION MECHANISM OF ALIPHATIC-ALCOHOLS BY PHENOXYL RADICALS
    VOEVODSKAIA, MV
    PROKOFIEV, AI
    KHUDIAKOV, IV
    DOKLADY AKADEMII NAUK SSSR, 1981, 258 (06): : 1390 - 1393
  • [42] CALCULATIONS ON ELECTRONIC SPECTRA OF ANILINO PHENOXYL AND BENZYL RADICALS
    HINCHLIFFE, A
    STAINBAN.RE
    ALI, MA
    THEORETICA CHIMICA ACTA, 1966, 5 (02): : 95 - +
  • [43] SUBSTITUENT EFFECTS IN ESR-SPECTRA OF PHENOXYL RADICALS
    DIXON, WT
    MOGHIMI, M
    MURPHY, D
    JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1974, 70 (10): : 1713 - 1720
  • [44] Proton reactivity and electronic structure of phenoxyl radicals in water
    Tripathi, GNR
    JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (13): : 2388 - 2397
  • [45] Redox properties and bond dissociations energies of phenoxyl radicals
    Grampp, G
    Landgraf, S
    Muresanu, C
    ELECTROCHIMICA ACTA, 2004, 49 (04) : 537 - 544
  • [46] INTERACTION OF PHENOXYL RADICALS WITH OXIDATION-PRODUCTS OF POLYPROPYLENE
    ROGINSKII, VA
    KOROLEVA, GP
    MILLER, VB
    BULLETIN OF THE ACADEMY OF SCIENCES OF THE USSR DIVISION OF CHEMICAL SCIENCE, 1974, 23 (06): : 1205 - 1208
  • [47] SINGLE-ELECTRON REDUCTION OF STABLE PHENOXYL RADICALS
    POKHODEN.VD
    BIDZILYA, VA
    KHIZHNYI, VA
    DOKLADY AKADEMII NAUK SSSR, 1969, 185 (03): : 644 - &
  • [48] RELATIVE ELECTRON SPIN DISTRIBUTIONS IN ANILINO AND PHENOXYL RADICALS
    ATHERTON, NM
    LAND, EJ
    PORTER, G
    TRANSACTIONS OF THE FARADAY SOCIETY, 1963, 59 (484): : 818 - &
  • [49] REVERSIBLE DIMERIZATION OF PHENOXYL RADICALS FORMED BY ANODIC-OXIDATION OF PHENOLATES - A QUANTITATIVE STUDY BY CYCLIC VOLTAMMETRY
    EVANS, DH
    JIMENEZ, PJ
    KELLY, MJ
    JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1984, 163 (1-2): : 145 - 157
  • [50] ADDITION OF RADICALS TO QUINONES .1. ESR STUDIES ON RADICALS FORMED FROM CHLOROQUINONES
    SIMANDI, TL
    ROCKENBAUER, A
    TUDOS, F
    MAGYAR KEMIAI FOLYOIRAT, 1979, 85 (01): : 7 - 14