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
Glucocorticoid: a word used to describe a class of steroid compounds that was derived from gluco se + cort ex + ster oid to reflect their: a) role in regulating glucose metabolism, b) adrenal cortex origin, and c) steroidal structure
By constantly draining the host's SAMe reserves for its own replication, the virus creates a severe systemic deficiency
Growth Factor Signaling BPC-157 enhances the activity of multiple growth factors, including VEGF (vascular endothelial growth factor) , TGF- (transforming growth factor beta) , and FGF (fibroblast growth factor)
European Journal of Endocrinology, 151 (4), 433438
2A), suggesting that oxidative stress leads to exhaustion of cellular GSH at earlier treatment which could be rapidly compensated through activated GCLC activity
