141 related articles for article (PubMed ID: 2854106)
1. Semi-quinone formation from the catechol and ortho-quinone metabolites of the antitumor agent VP-16-213.
van Maanen JM; Verkerk UH; Broersen J; Lafleur MV; De Vries J; Retèl J; Pinedo HM
Free Radic Res Commun; 1988; 4(6):371-84. PubMed ID: 2854106
[TBL] [Abstract][Full Text] [Related]
2. Effects of the ortho-quinone and catechol of the antitumor drug VP-16-213 on the biological activity of single-stranded and double-stranded phi X174 DNA.
van Maanen JM; Lafleur MV; Mans DR; van den Akker E; de Ruiter C; Kootstra PR; Pappie D; de Vries J; Retèl J; Pinedo HM
Biochem Pharmacol; 1988 Oct; 37(19):3579-89. PubMed ID: 2972290
[TBL] [Abstract][Full Text] [Related]
3. Role of the semi-quinone free radical of the anti-tumour agent etoposide (VP-16-213) in the inactivation of single- and double-stranded phi X174 DNA.
Mans DR; Retèl J; van Maanen JM; Lafleur MV; van Schaik MA; Pinedo HM; Lankelma J
Br J Cancer; 1990 Jul; 62(1):54-60. PubMed ID: 2167725
[TBL] [Abstract][Full Text] [Related]
4. Effects of oxygen radical scavengers on the inactivation of SS phi X174 DNA by the semi-quinone free radical of the antitumor agent etoposide.
Van Maanen JM; Mans DR; Lafleur MV; Van Schaik MA; de Vries J; Vermeulen NP; Retèl J; Lankelma J
Free Radic Res Commun; 1990; 9(2):69-86. PubMed ID: 2161389
[TBL] [Abstract][Full Text] [Related]
5. Reactions of glutathione with the catechol, the ortho-quinone and the semi-quinone free radical of etoposide. Consequences for DNA inactivation.
Mans DR; Lafleur MV; Westmijze EJ; Horn IR; Bets D; Schuurhuis GJ; Lankelma J; Retèl J
Biochem Pharmacol; 1992 Apr; 43(8):1761-8. PubMed ID: 1315544
[TBL] [Abstract][Full Text] [Related]
6. Characterization of free radicals produced during oxidation of etoposide (VP-16) and its catechol and quinone derivatives. An ESR Study.
Kalyanaraman B; Nemec J; Sinha BK
Biochemistry; 1989 May; 28(11):4839-46. PubMed ID: 2548593
[TBL] [Abstract][Full Text] [Related]
7. Inactivation of phi X174 DNA by the ortho-quinone derivative or its reduction product of the antitumor agent VP 16-213.
van Maanen JM; de Ruiter C; Kootstra PR; Lafleur MV; de Vries J; Retèl J; Pinedo HM
Eur J Cancer Clin Oncol; 1985 Oct; 21(10):1215-8. PubMed ID: 2934259
[TBL] [Abstract][Full Text] [Related]
8. Formation of different reaction products with single- and double-stranded DNA by the ortho-quinone and the semi-quinone free radical of etoposide (VP-16-213).
Mans DR; Lafleur MV; Westmijze EJ; van Maanen JM; van Schaik MA; Lankelma J; Retèl J
Biochem Pharmacol; 1991 Nov; 42(11):2131-9. PubMed ID: 1958231
[TBL] [Abstract][Full Text] [Related]
9. Ascorbate is the primary reductant of the phenoxyl radical of etoposide in the presence of thiols both in cell homogenates and in model systems.
Kagan VE; Yalowich JC; Day BW; Goldman R; Gantchev TG; Stoyanovsky DA
Biochemistry; 1994 Aug; 33(32):9651-60. PubMed ID: 8068642
[TBL] [Abstract][Full Text] [Related]
10. Reaction between ortho-semiquinones and oxygen: pulse radiolysis, electron spin resonance, and oxygen uptake studies.
Kalyanaraman B; Korytowski W; Pilas B; Sarna T; Land EJ; Truscott TG
Arch Biochem Biophys; 1988 Oct; 266(1):277-84. PubMed ID: 2845864
[TBL] [Abstract][Full Text] [Related]
11. Characterization of semiquinone free radicals formed from stilbene catechol estrogens. An ESR spin stabilization and spin trapping study.
Kalyanaraman B; Sealy RC; Liehr JG
J Biol Chem; 1989 Jul; 264(19):11014-9. PubMed ID: 2544580
[TBL] [Abstract][Full Text] [Related]
12. Peroxidative free radical formation and O-demethylation of etoposide(VP-16) and teniposide(VM-26).
Haim N; Roman J; Nemec J; Sinha BK
Biochem Biophys Res Commun; 1986 Feb; 135(1):215-20. PubMed ID: 3006680
[TBL] [Abstract][Full Text] [Related]
13. In vitro metabolism of etoposide (VP-16-213) by liver microsomes and irreversible binding of reactive intermediates to microsomal proteins.
Haim N; Nemec J; Roman J; Sinha BK
Biochem Pharmacol; 1987 Feb; 36(4):527-36. PubMed ID: 3030329
[TBL] [Abstract][Full Text] [Related]
14. Tyrosinase-induced phenoxyl radicals of etoposide (VP-16): interaction with reductants in model systems, K562 leukemic cell and nuclear homogenates.
Stoyanovsky D; Yalowich J; Gantchev T; Kagan V
Free Radic Res Commun; 1993; 19(6):371-86. PubMed ID: 8168727
[TBL] [Abstract][Full Text] [Related]
15. Antioxidant paradoxes of phenolic compounds: peroxyl radical scavenger and lipid antioxidant, etoposide (VP-16), inhibits sarcoplasmic reticulum Ca(2+)-ATPase via thiol oxidation by its phenoxyl radical.
Ritov VB; Goldman R; Stoyanovsky DA; Menshikova EV; Kagan VE
Arch Biochem Biophys; 1995 Aug; 321(1):140-52. PubMed ID: 7639514
[TBL] [Abstract][Full Text] [Related]
16. Bioreductive activation of catechol estrogen-ortho-quinones: aromatization of the B ring in 4-hydroxyequilenin markedly alters quinoid formation and reactivity.
Shen L; Pisha E; Huang Z; Pezzuto JM; Krol E; Alam Z; van Breemen RB; Bolton JL
Carcinogenesis; 1997 May; 18(5):1093-101. PubMed ID: 9163701
[TBL] [Abstract][Full Text] [Related]
17. NADPH-dependent covalent binding of [3H]paroxetine to human liver microsomes and S-9 fractions: identification of an electrophilic quinone metabolite of paroxetine.
Zhao SX; Dalvie DK; Kelly JM; Soglia JR; Frederick KS; Smith EB; Obach RS; Kalgutkar AS
Chem Res Toxicol; 2007 Nov; 20(11):1649-57. PubMed ID: 17907785
[TBL] [Abstract][Full Text] [Related]
18. Free radical formation from the antineoplastic agent VP 16-213.
Van Maanen JM; De Ruiter C; Kootstra PR; De Vries J; Pinedo HM
Free Radic Res Commun; 1986; 1(4):263-72. PubMed ID: 2849583
[TBL] [Abstract][Full Text] [Related]
19. One- and two-electron reduction of 2-methyl-1,4-naphthoquinone bioreductive alkylating agents: kinetic studies, free-radical production, thiol oxidation and DNA-strand-break formation.
Giulivi C; Cadenas E
Biochem J; 1994 Jul; 301 ( Pt 1)(Pt 1):21-30. PubMed ID: 8037673
[TBL] [Abstract][Full Text] [Related]
20. An electron spin resonance study of o-semiquinones formed during the enzymatic and autoxidation of catechol estrogens.
Kalyanaraman B; Sealy RC; Sivarajah K
J Biol Chem; 1984 Nov; 259(22):14018-22. PubMed ID: 6094535
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
