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Showing 13 to 18 of 18 entries
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Simultaneous 3-/4-Hydroxybenzoates Biodegradation and Arsenite Oxidation by .

Frontiers in microbiology

Fan X, Nie L, Shi K, Wang Q, Xia X, Wang G.
PMID: 31275273
Front Microbiol. 2019 Jun 18;10:1346. doi: 10.3389/fmicb.2019.01346. eCollection 2019.

Aromatic compounds and arsenic (As) often coexist in the environment. As(III)-oxidizing bacteria can oxidize the more toxic As(III) into the less toxic As(V), and As(V) is easily removed. Microorganisms with the ability to degrade aromatic compounds and oxidize arsenite...

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Fan X, Nie L, Shi K, et al. Simultaneous 3-/4-Hydroxybenzoates Biodegradation and Arsenite Oxidation by . Front Microbiol. 2019;10:1346doi: 10.3389/fmicb.2019.01346.
Fan, X., Nie, L., Shi, K., Wang, Q., Xia, X., & Wang, G. (2019). Simultaneous 3-/4-Hydroxybenzoates Biodegradation and Arsenite Oxidation by . Frontiers in microbiology, 101346. https://doi.org/10.3389/fmicb.2019.01346
Fan, Xia, et al. "Simultaneous 3-/4-Hydroxybenzoates Biodegradation and Arsenite Oxidation by ." Frontiers in microbiology vol. 10 (2019): 1346. doi: https://doi.org/10.3389/fmicb.2019.01346
Fan X, Nie L, Shi K, Wang Q, Xia X, Wang G. Simultaneous 3-/4-Hydroxybenzoates Biodegradation and Arsenite Oxidation by . Front Microbiol. 2019 Jun 18;10:1346. doi: 10.3389/fmicb.2019.01346. eCollection 2019. PMID: 31275273; PMCID: PMC6592069.
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Decarboxylative Coupling Reaction in ESI(-)-MS/MS of 4-Nitrobenzyl 4-Hydroxybenzoates: Triplet Ion-Neutral Complex-Mediated 4-Nitrobenzyl Transfer.

Journal of the American Society for Mass Spectrometry

Zhang X, Bai X, Fang L, Jiang K, Li Z.
PMID: 26926444
J Am Soc Mass Spectrom. 2016 May;27(5):940-3. doi: 10.1007/s13361-016-1339-7. Epub 2016 Feb 29.

In negative electrospray ionization mass spectrometry of 4-nitrobenzyl 4-hydroxybenzoates, a decarboxylation reaction, which was significantly promoted by the presence of a nitro group on the benzyl group, competed with radical elimination reactions. Density functional theory calculations indicated that decarboxylation...

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Zhang X, Bai X, Fang L, et al. Decarboxylative Coupling Reaction in ESI(-)-MS/MS of 4-Nitrobenzyl 4-Hydroxybenzoates: Triplet Ion-Neutral Complex-Mediated 4-Nitrobenzyl Transfer. J Am Soc Mass Spectrom. 2016;27(5):940-3doi: 10.1007/s13361-016-1339-7.
Zhang, X., Bai, X., Fang, L., Jiang, K., & Li, Z. (2016). Decarboxylative Coupling Reaction in ESI(-)-MS/MS of 4-Nitrobenzyl 4-Hydroxybenzoates: Triplet Ion-Neutral Complex-Mediated 4-Nitrobenzyl Transfer. Journal of the American Society for Mass Spectrometry, 27(5), 940-3. https://doi.org/10.1007/s13361-016-1339-7
Zhang, Xiaoping, et al. "Decarboxylative Coupling Reaction in ESI(-)-MS/MS of 4-Nitrobenzyl 4-Hydroxybenzoates: Triplet Ion-Neutral Complex-Mediated 4-Nitrobenzyl Transfer." Journal of the American Society for Mass Spectrometry vol. 27,5 (2016): 940-3. doi: https://doi.org/10.1007/s13361-016-1339-7
Zhang X, Bai X, Fang L, Jiang K, Li Z. Decarboxylative Coupling Reaction in ESI(-)-MS/MS of 4-Nitrobenzyl 4-Hydroxybenzoates: Triplet Ion-Neutral Complex-Mediated 4-Nitrobenzyl Transfer. J Am Soc Mass Spectrom. 2016 May;27(5):940-3. doi: 10.1007/s13361-016-1339-7. Epub 2016 Feb 29. PMID: 26926444.
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Salicylate and liver glutathione.

British journal of pharmacology and chemotherapy

Sproull DH.
PMID: 19108147
Br J Pharmacol Chemother. 1961 Apr;16(2):180-7. doi: 10.1111/j.1476-5381.1961.tb00311.x.

The effects of sodium salicylate, benzoate, gentisate, m- and p-hydroxybenzoates, antipyrine, and 2:4-dinitrophenol on the reduced glutathione concentration of rat liver were determined. An increase in concentration in the male, but not in the female, rats was found after...

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Sproull DH. Salicylate and liver glutathione. Br J Pharmacol Chemother. 1961;16(2):180-7doi: 10.1111/j.1476-5381.1961.tb00311.x.
Sproull, D. H. (1961). Salicylate and liver glutathione. British journal of pharmacology and chemotherapy, 16(2), 180-7. https://doi.org/10.1111/j.1476-5381.1961.tb00311.x
Sproull, D H. "Salicylate and liver glutathione." British journal of pharmacology and chemotherapy vol. 16,2 (1961): 180-7. doi: https://doi.org/10.1111/j.1476-5381.1961.tb00311.x
Sproull DH. Salicylate and liver glutathione. Br J Pharmacol Chemother. 1961 Apr;16(2):180-7. doi: 10.1111/j.1476-5381.1961.tb00311.x. PMID: 19108147; PMCID: PMC1481952.
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Influence of alternate electron acceptors on the metabolic fate of hydroxybenzoate isomers in anoxic aquifer slurries.

Applied and environmental microbiology

Kuhn EP, Suflita JM, Rivera MD, Young LY.
PMID: 16347868
Appl Environ Microbiol. 1989 Mar;55(3):590-8. doi: 10.1128/aem.55.3.590-598.1989.

The biodegradation of hydroxybenzoate isomers was investigated with samples obtained from two sites within a shallow anoxic aquifer. The metabolic fates of the substrates were compared in denitrifying, sulfate-reducing, and methanogenic incubations. Under the latter two conditions, phenol was...

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Kuhn EP, Suflita JM, Rivera MD, et al. Influence of alternate electron acceptors on the metabolic fate of hydroxybenzoate isomers in anoxic aquifer slurries. Appl Environ Microbiol. 1989;55(3):590-8doi: 10.1128/aem.55.3.590-598.1989.
Kuhn, E. P., Suflita, J. M., Rivera, M. D., & Young, L. Y. (1989). Influence of alternate electron acceptors on the metabolic fate of hydroxybenzoate isomers in anoxic aquifer slurries. Applied and environmental microbiology, 55(3), 590-8. https://doi.org/10.1128/aem.55.3.590-598.1989
Kuhn, E P, et al. "Influence of alternate electron acceptors on the metabolic fate of hydroxybenzoate isomers in anoxic aquifer slurries." Applied and environmental microbiology vol. 55,3 (1989): 590-8. doi: https://doi.org/10.1128/aem.55.3.590-598.1989
Kuhn EP, Suflita JM, Rivera MD, Young LY. Influence of alternate electron acceptors on the metabolic fate of hydroxybenzoate isomers in anoxic aquifer slurries. Appl Environ Microbiol. 1989 Mar;55(3):590-8. doi: 10.1128/aem.55.3.590-598.1989. PMID: 16347868; PMCID: PMC184165.
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Ion mobility and clustering of sodium hydroxybenzoates in aqueous solutions: a molecular dynamics simulation study.

Physical chemistry chemical physics : PCCP

Gujt J, Podlipnik Č, Bešter-Rogač M, Spohr E.
PMID: 25099487
Phys Chem Chem Phys. 2014 Sep 28;16(36):19314-26. doi: 10.1039/c4cp02425g.

The relative position of the hydroxylic and the carboxylic group in the isomeric hydroxybenzoate (HB) anions is known to have a large impact on transport properties of this species. It also influences crucially the self-organisation of cationic surfactants. In...

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Gujt J, Podlipnik Č, Bešter-Rogač M, et al. Ion mobility and clustering of sodium hydroxybenzoates in aqueous solutions: a molecular dynamics simulation study. Phys Chem Chem Phys. 2014;16(36):19314-26doi: 10.1039/c4cp02425g.
Gujt, J., Podlipnik, �. �., Bešter-Rogač, M., & Spohr, E. (2014). Ion mobility and clustering of sodium hydroxybenzoates in aqueous solutions: a molecular dynamics simulation study. Physical chemistry chemical physics : PCCP, 16(36), 19314-26. https://doi.org/10.1039/c4cp02425g
Gujt, Jure, et al. "Ion mobility and clustering of sodium hydroxybenzoates in aqueous solutions: a molecular dynamics simulation study." Physical chemistry chemical physics : PCCP vol. 16,36 (2014): 19314-26. doi: https://doi.org/10.1039/c4cp02425g
Gujt J, Podlipnik Č, Bešter-Rogač M, Spohr E. Ion mobility and clustering of sodium hydroxybenzoates in aqueous solutions: a molecular dynamics simulation study. Phys Chem Chem Phys. 2014 Sep 28;16(36):19314-26. doi: 10.1039/c4cp02425g. PMID: 25099487.
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Geranyl Phenyl Ethers from the New Zealand Liverwort Trichocolea hatcheri.

Journal of natural products

Baek SH, Perry NB, Weavers RT, Tangney RS.
PMID: 9548839
J Nat Prod. 1998 Jan 23;61(1):126-9. doi: 10.1021/np970379b.

Methyl 4-(geranyloxy)-3-hydroxybenzoate (6), previously unreported, has been identified from the New Zealand liverwort Trichocolea hatcheri. Four new related 3-hydroxybenzoates 7-10 were also found, with a carbonyl at C-5 of the geranyl group and various double bond arrangements. Two known...

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Baek SH, Perry NB, Weavers RT, et al. Geranyl Phenyl Ethers from the New Zealand Liverwort Trichocolea hatcheri. J Nat Prod. 1998;61(1):126-9doi: 10.1021/np970379b.
Baek, S. H., Perry, N. B., Weavers, R. T., & Tangney, R. S. (1998). Geranyl Phenyl Ethers from the New Zealand Liverwort Trichocolea hatcheri. Journal of natural products, 61(1), 126-9. https://doi.org/10.1021/np970379b
Baek, et al. "Geranyl Phenyl Ethers from the New Zealand Liverwort Trichocolea hatcheri." Journal of natural products vol. 61,1 (1998): 126-9. doi: https://doi.org/10.1021/np970379b
Baek SH, Perry NB, Weavers RT, Tangney RS. Geranyl Phenyl Ethers from the New Zealand Liverwort Trichocolea hatcheri. J Nat Prod. 1998 Jan 23;61(1):126-9. doi: 10.1021/np970379b. PMID: 9548839.
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Showing 13 to 18 of 18 entries