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3. Oxidation of catechol in plants. II. Enzymic conversion of catechol to diphenylenedioxide 2,3-quinone in the leaves of Tecoma stans L. Kandaswami C; Vaidyanathan CS Indian J Biochem Biophys; 1973 Mar; 10(1):23-6. PubMed ID: 4204898 [No Abstract] [Full Text] [Related]
4. Direct evidence for quinone-quinone methide tautomerism during tyrosinase catalyzed oxidation of 4-allylcatechol. Sugumaran M; Bolton J Biochem Biophys Res Commun; 1995 Aug; 213(2):469-74. PubMed ID: 7646501 [TBL] [Abstract][Full Text] [Related]
5. A chromogenic assay for catecholoxidases based on the addition of L-proline to quinones. Rzepecki LM; Waite JH Anal Biochem; 1989 Jun; 179(2):375-81. PubMed ID: 2774185 [TBL] [Abstract][Full Text] [Related]
6. The participation of a quinone in the enzymic reduction of glycine by Clostridium sticklandii. STADTMAN TC Biochem Z; 1958; 331(1):46-8. PubMed ID: 13628592 [No Abstract] [Full Text] [Related]
7. Semiquinone anion radicals from addition of amino acids, peptides, and proteins to quinones derived from oxidation of catechols and catecholamines. An ESR spin stabilization study. Kalyanaraman B; Premovic PI; Sealy RC J Biol Chem; 1987 Aug; 262(23):11080-7. PubMed ID: 3038907 [TBL] [Abstract][Full Text] [Related]
8. Oxidation of dihydrothiamine by quinone derivatives. MITSUDA H; HASHITANI Y; KAWAI F J Vitaminol (Kyoto); 1961 Dec; 7():256-64. PubMed ID: 14474707 [No Abstract] [Full Text] [Related]
9. Radical-pair energetics and decay mechanisms in reaction centers containing anthraquinones, naphthoquinones or benzoquinones in place of ubiquinone. Woodbury NW; Parson WW; Gunner MR; Prince RC; Dutton PL Biochim Biophys Acta; 1986 Aug; 851(1):6-22. PubMed ID: 3524681 [TBL] [Abstract][Full Text] [Related]
10. Semiquinone anion radicals of catechol(amine)s, catechol estrogens, and their metal ion complexes. Kalyanaraman B; Felix CC; Sealy RC Environ Health Perspect; 1985 Dec; 64():185-98. PubMed ID: 3007089 [TBL] [Abstract][Full Text] [Related]
11. 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]
13. The quantum efficiency of the photochemical reduction of quinone and ferricyanide by lyophilized and whole Chlorella cells. SCHWARTZ M Arch Biochem Biophys; 1955 Nov; 59(1):5-16. PubMed ID: 13269151 [No Abstract] [Full Text] [Related]
14. A dopaquinone model that mimics the water addition step of cofactor biogenesis in copper amine oxidases. Ling KQ; Sayre LM J Am Chem Soc; 2005 Apr; 127(13):4777-84. PubMed ID: 15796543 [TBL] [Abstract][Full Text] [Related]
15. Cytochrome P450 isoforms catalyze formation of catechol estrogen quinones that react with DNA. Zhang Y; Gaikwad NW; Olson K; Zahid M; Cavalieri EL; Rogan EG Metabolism; 2007 Jul; 56(7):887-94. PubMed ID: 17570247 [TBL] [Abstract][Full Text] [Related]
16. [On fermentation and quinone in cell metabolism]. KIESOW L Z Naturforsch B; 1960 Mar; 15B():174-9. PubMed ID: 13853379 [No Abstract] [Full Text] [Related]
17. A rapid and sensitive micro-assay to determine the capacity of quinones to undergo redox cycling. Hart LA; van der Wal NA; Koster AS; Labadie RP Toxicol Lett; 1989 Aug; 48(2):151-7. PubMed ID: 2772921 [TBL] [Abstract][Full Text] [Related]
18. p-Quinone methides are the major decomposition products of catechol estrogen o-quinones. Bolton JL; Shen L Carcinogenesis; 1996 May; 17(5):925-9. PubMed ID: 8640939 [TBL] [Abstract][Full Text] [Related]
19. [On orthophosphoric acid and carbon dioxide in quinone catalysis in the living cell]. KIESOW L Z Naturforsch B; 1960 May; 15B():293-7. PubMed ID: 13853381 [No Abstract] [Full Text] [Related]
20. The photochemical reduction of quinone and ferricyanide by lyophilized Chlorella cells. SCHWARTZ M Biochim Biophys Acta; 1956 Dec; 22(3):463-70. PubMed ID: 13382875 [No Abstract] [Full Text] [Related] [Next] [New Search]