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Year Number of Results
1964 1
1979 1
1980 1
1981 1
1982 3
1985 1
1986 2
1988 1
1993 1
1995 1
1996 1
1997 1
1998 1
1999 2
2001 1
2002 1
2003 3
2004 1
2006 1
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2008 1
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2011 1
2012 1
2013 3
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39 results

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Page 1
Metabolism of 2,6-dimethylnaphthalene by rat liver microsomes and effect of its administration on glutathione depletion in vivo.
Shamsuddin ZA, Rahimtula AD. Shamsuddin ZA, et al. Drug Metab Dispos. 1986 Nov-Dec;14(6):724-32. Drug Metab Dispos. 1986. PMID: 2877834
Metabolism of the environmental contaminant 2,6-dimethylnaphthalene (2,6-DMN) by rat liver microsomes and an NADPH-regenerating system led to the formation of three ring oxidation metabolites--2,6-dimethyl-3-naphthol, 2,6-dimethyl-3,4-naphthoquinone, and 3,4- …
Metabolism of the environmental contaminant 2,6-dimethylnaphthalene (2,6-DMN) by rat liver microsomes and an NADPH-rege …
Metabolism of 2,6-dimethylnaphthalene by flavobacteria.
Barnsley EA. Barnsley EA. Appl Environ Microbiol. 1988 Feb;54(2):428-33. doi: 10.1128/aem.54.2.428-433.1988. Appl Environ Microbiol. 1988. PMID: 3355133 Free PMC article.
Flavobacteria that were able to grow on 2,6-dimethylnaphthalene (2,6-DMN) were isolated from soil. Most were able to oxidize a broad range of aromatic hydrocarbons after growth on 2,6-DMN at rates comparable to that of the oxidation of 2,6-DMN itself. ...
Flavobacteria that were able to grow on 2,6-dimethylnaphthalene (2,6-DMN) were isolated from soil. Most were able to ox …
Structures of 2,6-disubstituted naphthalenes.
Kaduk JA, Golab JT. Kaduk JA, et al. Acta Crystallogr B. 1999 Feb 1;55(Pt 1):85-94. doi: 10.1107/s0108768198008945. Acta Crystallogr B. 1999. PMID: 10927342
The crystal structures of 2,6-naphthalenedicarboxylic acid (NDA) and dimethyl 2,6-naphthalenedicarboxylate (NDC) have been solved ab initio using a combination of X-ray powder diffraction and computational chemistry techniques. These two crystal structures, and that of 2, …
The crystal structures of 2,6-naphthalenedicarboxylic acid (NDA) and dimethyl 2,6-naphthalenedicarboxylate (NDC) have been solved ab initio …
Biotransformation of p-xylene and 2,6-dimethylnaphthalene by xylene monooxygenase cloned from a Sphingomonas isolate.
Bramucci M, Singh M, Nagarajan V. Bramucci M, et al. Appl Microbiol Biotechnol. 2002 Sep;59(6):679-84. doi: 10.1007/s00253-002-1068-7. Epub 2002 Jul 13. Appl Microbiol Biotechnol. 2002. PMID: 12226724
Sphingomonas strain ASU1 was isolated from an industrial wastewater bioreactor and grew on 2,6-dimethylnaphthalene (2,6-DMN) as the sole carbon/energy source. ...
Sphingomonas strain ASU1 was isolated from an industrial wastewater bioreactor and grew on 2,6-dimethylnaphthalene (2,6 …
Vapor pressures, thermodynamic stability, and fluorescence properties of three 2,6-alkyl naphthalenes.
Santos AF, Oliveira JA, Ribeiro da Silva MD, Monte MJ. Santos AF, et al. Chemosphere. 2016 Mar;146:173-81. doi: 10.1016/j.chemosphere.2015.11.114. Epub 2015 Dec 21. Chemosphere. 2016. PMID: 26716880
The thermodynamic stability of the compounds in both the crystalline and gaseous phases was evaluated by the determination of the Gibbs energies of formation and compared with the ones reported in the literature for 2,6-dimethylnaphthalene. From fluorescence …
The thermodynamic stability of the compounds in both the crystalline and gaseous phases was evaluated by the determination of the Gibbs ener …
Microbial oxidation of dimethylnaphthalene isomers.
Miyachi N, Tanaka T, Suzuki T, Hotta Y, Omori T. Miyachi N, et al. Appl Environ Microbiol. 1993 May;59(5):1504-6. doi: 10.1128/aem.59.5.1504-1506.1993. Appl Environ Microbiol. 1993. PMID: 8517744 Free PMC article.
Three bacterial strains, identified as Alcaligenes sp. strain D-59 and Pseudomonas sp. strains D-87 and D-186, capable of growing on 2,6-dimethylnaphthalene (2,6-DMN) as the sole source of carbon and energy were isolated from soil samples. 2,6-Naphthalene dic …
Three bacterial strains, identified as Alcaligenes sp. strain D-59 and Pseudomonas sp. strains D-87 and D-186, capable of growing on 2 …
BETA-CAROTENE: THERMAL DEGRADATION.
MADER I. MADER I. Science. 1964 May 1;144(3618):533-4. doi: 10.1126/science.144.3618.533. Science. 1964. PMID: 14194098
Thermal treatment of crystalline beta-carotene (240 degrees C in a vacuum) results in the formation of a volatile fraction containing chiefly aromatic hydrocarbons such as toluene, m- and p-xylene, 2,6-dimethylnaphthalene, and ionene. These compounds have bee …
Thermal treatment of crystalline beta-carotene (240 degrees C in a vacuum) results in the formation of a volatile fraction containing chiefl …
39 results