Uptake system of lignin-derived aromatic acids in promising Sphingomonadaceae strains for lignin valorization through biological funneling. [PDF]
Fujita M +4 more
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Analysis of bioactive compounds in Gardenia jasminoides from different regions by UFLC/QTRAP-MS and PCA. [PDF]
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Phenolic compounds profiling of nine dogwood species (<i>Cornus</i> L.) leaves. [PDF]
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Profile of Free and Conjugated Phenolic Compounds of Okra Pods Subjected to High-Humidity Hot-Air Impingement Blanching (HHAIB). [PDF]
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The enterobactin biosynthetic intermediate 2,3-dihydroxybenzoic acid is a competitive inhibitor of the Escherichia coli isochorismatase EntB. [PDF]
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TEAC antioxidant activity of 4-hydroxybenzoates
Free Radical Biology and Medicine, 1999The influence of pH, intrinsic electron donating capacity, and intrinsic hydrogen atom donating capacity on the antioxidant potential of series of hydroxy and fluorine substituted 4-hydroxybenzoates was investigated experimentally and also on the basis of computer calculations.
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Solubility of Hydroxybenzoic Acids and Hydroxybenzoates
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Interaction of 3-Hydroxybenzoate with 3-Hydroxybenzoate-6-hydroxylase
Biotechnology Progress, 2001The gradual quenching of the emission fluorescence of 3-HBA in the visible region upon titration with 3-HBA-6-hydroxylase and distinct changes in the near-UV circular dichroic spectrum of the enzyme in the presence of substrate suggest the formation of a stable enzyme-substrate complex.
SURESH, S, DASGUPTA, D
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Excited-state proton transfer of 3-hydroxybenzoic acid and 4-hydroxybenzoic acid
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2010The excited-state proton transfer of 3-hydroxybenzoic acid and 4-hydroxybenzoic acid was studied by time-resolved laser-induced fluorescence spectroscopy with ultra-short laser pulses. The excited-state reactions were identified in aqueous media as a function of the pH value.
Vulpius, D., Geipel, G., Bernhard, G.
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Metabolism of 1-hydroxybenzo[a]pyrene
Chemico-Biological Interactions, 1981Abstract A metabolite of the known carcinogen benzo[ a ]pyrene (BP), 1-hydroxybenzo[ a ]pyrene 1-BPOH, is further metabolized by rat liver homogenate and microsomes. This oxidation is shown to be enzyme-catalyzed and dependent upon the presence of NADH and NADPH. Isolation of the final product yielded the BP-1,6-dione.
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