Kagan VE - Search Results

1

Interactions of phenoxyl radical of antitumor drug, etoposide, with reductants in solution and in cell and nuclear homogenates: electron spin resonance and high-performance liquid chromatography.

Gantchev TG, van Lier JE, Stoyanovsky DA, Yalowich JC, Kagan VE. Gantchev TG, et al. Among authors: kagan ve. Methods Enzymol. 1994;234:631-42. doi: 10.1016/0076-6879(94)34134-6. Methods Enzymol. 1994. PMID: 7808339 No abstract available.

2

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. Stoyanovsky D, et al. Free Radic Res Commun. 1993;19(6):371-86. doi: 10.3109/10715769309056527. Free Radic Res Commun. 1993. PMID: 8168727

3

Assay of ubiquinones and ubiquinols as antioxidants.

Kagan VE, Serbinova EA, Stoyanovsky DA, Khwaja S, Packer L. Kagan VE, et al. Methods Enzymol. 1994;234:343-54. doi: 10.1016/0076-6879(94)34104-4. Methods Enzymol. 1994. PMID: 7808306 No abstract available.

4

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. Kagan VE, et al. Biochemistry. 1994 Aug 16;33(32):9651-60. doi: 10.1021/bi00198a034. Biochemistry. 1994. PMID: 8068642

5

Phenoxyl radical-induced thiol-dependent generation of reactive oxygen species: implications for benzene toxicity.

Stoyanovsky DA, Goldman R, Claycamp HG, Kagan VE. Stoyanovsky DA, et al. Among authors: kagan ve. Arch Biochem Biophys. 1995 Mar 10;317(2):315-23. doi: 10.1006/abbi.1995.1169. Arch Biochem Biophys. 1995. PMID: 7893144

6

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. Ritov VB, et al. Among authors: kagan ve. Arch Biochem Biophys. 1995 Aug 1;321(1):140-52. doi: 10.1006/abbi.1995.1379. Arch Biochem Biophys. 1995. PMID: 7639514

7

Reduction of phenoxyl radicals by thioredoxin results in selective oxidation of its SH-groups to disulfides. An antioxidant function of thioredoxin.

Goldman R, Stoyanovsky DA, Day BW, Kagan VE. Goldman R, et al. Among authors: kagan ve. Biochemistry. 1995 Apr 11;34(14):4765-72. doi: 10.1021/bi00014a034. Biochemistry. 1995. PMID: 7718583

8

Phenoxyl radicals of etoposide (VP-16) can directly oxidize intracellular thiols: protective versus damaging effects of phenolic antioxidants.

Tyurina YY, Tyurin VA, Yalowich JC, Quinn PJ, Claycamp HG, Schor NF, Pitt BR, Kagan VE. Tyurina YY, et al. Among authors: kagan ve. Toxicol Appl Pharmacol. 1995 Apr;131(2):277-88. doi: 10.1006/taap.1995.1070. Toxicol Appl Pharmacol. 1995. PMID: 7716769

9

Endogenous ascorbate regenerates vitamin E in the retina directly and in combination with exogenous dihydrolipoic acid.

Stoyanovsky DA, Goldman R, Darrow RM, Organisciak DT, Kagan VE. Stoyanovsky DA, et al. Among authors: kagan ve. Curr Eye Res. 1995 Mar;14(3):181-9. doi: 10.3109/02713689509033513. Curr Eye Res. 1995. PMID: 7796601

10

Ascorbate/iron activates Ca(2+)-release channels of skeletal sarcoplasmic reticulum vesicles reconstituted in lipid bilayers.

Stoyanovsky DA, Salama G, Kagan VE. Stoyanovsky DA, et al. Among authors: kagan ve. Arch Biochem Biophys. 1994 Jan;308(1):214-21. doi: 10.1006/abbi.1994.1030. Arch Biochem Biophys. 1994. PMID: 8311455

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