E ve C vitaminlerinin yeniden retimine yardm eder
Antioxidants (Basel) 14 (5), 527
BBR 3-(3-carboxy-benzyloxy)-oleanolic acid - 3-(4-carboxy-benzyloxy)-28-[4-butyric((s)-1-carboxyphenylethyl)-amide]-DELTA12-oleanene - 3-(4-carboxy-benzyloxy)-oleanolic acid - 3-(biphenyl-4-ylmethyl)-6-hydroxy-2-(4-hydroxybenzyl)-4H-chromen-4-one - 3-(carboxy-fluoro-methoxy)-6-chloro-benzo(b)thiophene-2-carboxylic acid - - 3-(carboxymethoxy)-2-naphthoic acid - - 3-(carboxymethoxy)-5-((cyclohexylmethyl)-amino)thieno(3,2-b)(1)benzothiophene-2-carboxylic acid - - 3-(carboxymethoxy)-5-(cyclohexylamino)-thieno(3,2-b)(1)benzothiophene-2-carboxylic acid - - 3-(carboxymethoxy)-5-chlorothieno(3,2-b)(1)benzothiophene-2-carboxylic acid - - 3-(carboxymethoxy)-6-((1-(ethylsulfonyl)-piperidin-4-yl)amino)thieno(3,2-b)(1)benzothiophene-2-carboxylic acid - - 3-(carboxymethoxy)-6-((cyclohexylmethyl)-amino)thieno(3,2-b)(1)benzothiophene-2-carboxylic acid - - 3-(carboxymethoxy)-6-(cyclohexylamino)-thieno(3,2-b)(1)benzothiophene-2-carboxylic acid - - 3-(carboxymethoxy)-6-(tetrahydro-2H-pyran-4-ylamino)thieno(3,2-b)(1)benzothiophene-2-carboxylic acid - - 3-(carboxymethoxy)-6-chlorothieno(3,2-b)(1)benzothiophene-2-carboxylic acid - - 3-(carboxymethoxy)-6-methylthieno(3,2-c)pyridine-2-carboxylic acid - - 3-(carboxymethoxy)benzo(b)thiophene-2-carboxylic acid - - 3-(carboxymethoxy)furo(2,3-b)pyridine-2-carboxylic acid - - 3-(carboxymethoxy)thieno(2,3-b)pyridine-2-carboxylic acid - reversible, competitive 3-(carboxymethoxy)thieno(3,2-b)(1)benzo-thiophene-2-carboxylic acid - - 3-(carboxymethoxy)thieno(3,2-b)pyridine-2-carboxylic acid - - 3-(carboxymethoxy)thieno(3,2-b)thiophene-2-carboxylic acid - - 3-([2-chloro-6-methoxy-4-[(E)-(3-oxo[1,3]thiazolo[3,2-a]benzimidazol-2(3H)-ylidene)methyl]phenoxy]methyl)benzoic acid - 3-benzyl-7-hydroxy-2-(4-hydroxybenzyl)-4H-chromen-4-one 10% inhibition of LMW-PTP isozymes 1 and 2,no inhibition of PTP-B1, at 0.015 mM 3-benzyloxy-oleanolic acid - 3-bromo-4-[(2,3-dibromo-4,5-dihydroxyphenyl)methyl]-5-(propoxymethyl)benzene-1,2-diol 86.15% inhibition at 0.02 mg/ml 3-bromo-4-[(2,3-dibromo-4,5-dihydroxyphenyl)methyl]-5-[(2-methylpropoxy)methyl]benzene-1,2-diol 96.25% inhibition at 0.02 mg/ml 3-bromo-4-[(2,3-dibromo-4,5-dihydroxyphenyl)methyl]-5-[[(propan-2-yl)oxy]methyl]benzene-1,2-diol - 3-butyl-7-(2,4-dihydroxy-6-pentylphenoxy)-3,5-dimethoxy-2-benzofuran-1(3H)-one - a pseudodepsidone-type compound, isolated from a methanol extract of the Antarctic lichen Stereocaulon alpinum 3-carboxymethoxy-6-(4-hydroxyphenyl)-benzo(b)-thiophene-2-carboxylic acid - - 3-carboxymethoxy-6-(5-methyl-1-phenyl-1H-pyrazol-3-ylcarbamoyl)-benzo(b)thiophene-2-carboxylic acid - - 3-carboxymethoxy-6-chloro-benzo(b)-thiophene-2-carboxylic acid - - 3-carboxymethoxy-6-phenylbenzo(b)-thiophene-2-carboxylic acid - - 3-carboxymethoxy-6-thiophen-2-yl-benzo(b)-thiophene-2-carboxylic acid - - 3-carboxymethoxy-7-chloro-benzo(b)-thiophene-2-carboxylic acid - - 3-carboxymethoxy-7-methyl-benzo(b)-thiophene-2-carboxylic acid - - 3-carboxymethoxy-naphtho(1,2-b)thiophene-2-carboxylic acid - - 3-carboxymethoxy-thieno(3,2-c)quinoline-2-carboxylic acid - - 3-carboxypropanoyloxy-oleanolic acid - 3-chlorobenzenecarboperoxoic acid - complete inhibition at 150 mM 3-dehydroxy-oleanolic acid - 3-ethyl oxalyl-oleanolic acid - 3-hydroxy-4-(methoxycarbonyl)-2,5-dimethylphenyl 3-acetyl-2,4-dihydroxy-6-methylbenzoate - isolated from a methanol extract of the Antarctic lichen Stereocaulon alpinum 3-hydroxy-4-(methoxycarbonyl)-5-methylphenyl 4-(beta-D-galactopyranosyloxy)-2-hydroxy-6-pentadecylbenzoate - - 3-methyl-2-butenal - 95% remaining activity at 0.5 mM 3-methylene-oleanolic acid - 3-oxalyl-oleanolic acid - 3-oxo-oleanolic acid - 3-[(1-butyl-1,6-dimethoxy-3-oxo-1,3-dihydro-2-benzofuran-4-yl)oxy]-4,6-dihydroxy-2-pentylbenzoic acid - a pseudodepsidone-type compound, isolated from a methanol extract of the Antarctic lichen Stereocaulon alpinum 3-[(2-nitrophenyl)hydrazono]-2-oxo-2,3-dihydro-1H-indole-5-sulfonamide - - 3-[(2-nitrophenyl)hydrazono]-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid 4-chlorobenzylamide - - 3-[(3-[(E)-[3-(4-carboxybenzyl)-2,4-dioxo-1,3-thiazolidin-5-ylidene]methyl]phenoxy)methyl]benzoic acid - 3-[(4-[(Z)-[3-(4-carboxybenzyl)-2,4-dioxo-1,3-thiazolidin-5-ylidene]methyl]phenoxy)methyl]benzoic acid - 3-[(E)-(3-oxo[1,3]thiazolo[3,2-a]benzimidazol-2(3H)-ylidene)methyl]benzoic acid - 3-[2,5-dimethyl-3-[(3-oxo-2,3-dihydro[1,3]thiazolo[3,2-a]benzimidazol-2-yl)methyl]-1H-pyrrol-1-yl]benzoic acid irreversible inhibition, detailed kinetic analysis of the interaction between E4 and the catalytic domain of enzyme STEP, overview
European Journal of Endocrinology, 151 (4), 433438
These enzymes use endogenous NADPH to affect the redox couple and recycle lipoate to the reduced form: DHLA
2A), suggesting that oxidative stress leads to exhaustion of cellular GSH at earlier treatment which could be rapidly compensated through activated GCLC activity
