[DOI] [PMC free article] [PubMed] [Google Scholar] Hong R, Zhou Y, Tian X
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
It also helps your immune system, mental health, and more
Monitoring & Adjustments Functional Markers: VO max, mitochondrial DNA copy number (optional), and fatigue scales
Acetaldehyde increases skin temperature, making you feel hot and flushed
