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The following term was not found in PubMed: -10-phenylsulfanylcyclodec-5-en-1-one
Page 1
Phenolic bisabolane sesquiterpenoids from a Thai mangrove endophytic fungus, Aspergillus sp. xy02.
Wang P, Yu JH, Zhu K, Wang Y, Cheng ZQ, Jiang CS, Dai JG, Wu J, Zhang H. Wang P, et al. Fitoterapia. 2018 Jun;127:322-327. doi: 10.1016/j.fitote.2018.02.031. Epub 2018 Mar 12. Fitoterapia. 2018. PMID: 29544761
Seven new phenolic bisabolane sesquiterpenoids, (7R,10S)-7,10-epoxysydonic acid (1), (7S,10S)-7,10-epoxysydonic acid (2), (7R,11S)-7,12-epoxysydonic acid (3), (7S,11S)-7,12-epoxysydonic acid (4), 7-deoxy-7,14-didehydro-12-hydroxysydonic acid (5), (Z)-7-deoxy-7,8-did …
Seven new phenolic bisabolane sesquiterpenoids, (7R,10S)-7,10-epoxysydonic acid (1), (7S,10S)-7,10-epoxysydonic acid (2), (7R, …
Biochemical characterization of the oxygenation of unsaturated fatty acids by the dioxygenase and hydroperoxide isomerase of Pseudomonas aeruginosa 42A2.
Martínez E, Hamberg M, Busquets M, Díaz P, Manresa A, Oliw EH. Martínez E, et al. J Biol Chem. 2010 Mar 26;285(13):9339-9345. doi: 10.1074/jbc.M109.078147. Epub 2010 Jan 14. J Biol Chem. 2010. PMID: 20075076 Free PMC article.
We have studied oxygenation of fatty acids by cell extract of Pseudomonas aeruginosa 42A2. Oleic acid ((9Z)-18:1) was transformed to (10S)-hydroperoxy-(8E)-octadecenoic acid ((10S)-HPOME) and to (7S,10S)-dihydroxy-(8E)-octadecenoic acid (7,10-DiHOME). ...A se …
We have studied oxygenation of fatty acids by cell extract of Pseudomonas aeruginosa 42A2. Oleic acid ((9Z)-18:1) was transformed to (10S
Metabolites contributing to Rhizoctonia solani AG-1-IA maturation and sclerotial differentiation revealed by UPLC-QTOF-MS metabolomics.
Hu W, Pan X, Abbas HMK, Li F, Dong W. Hu W, et al. PLoS One. 2017 May 10;12(5):e0177464. doi: 10.1371/journal.pone.0177464. eCollection 2017. PLoS One. 2017. PMID: 28489938 Free PMC article.
Our results revealed that during maturation, the metabolic levels of N2-acetyl-L-ornithine, 3,1'-(OH)2-Gamma-carotene, (5Z,7E)-(1S,3R)-24,24-difluoro-24a-homo-9,10-seco-5,7,10(19)-cholestatrien-1,3,25-triol, stoloniferone O, PA(O-18:0/12:0), PA(P-16:0/14:0), PA(P-16:0/16:( …
Our results revealed that during maturation, the metabolic levels of N2-acetyl-L-ornithine, 3,1'-(OH)2-Gamma-carotene, (5Z,7E)-(1S,3R …
Altered SPMs and age-associated decrease in brain DHA in APOE4 female mice.
Martinsen A, Tejera N, Vauzour D, Harden G, Dick J, Shinde S, Barden A, Mori TA, Minihane AM. Martinsen A, et al. FASEB J. 2019 Sep;33(9):10315-10326. doi: 10.1096/fj.201900423R. Epub 2019 Jul 29. FASEB J. 2019. PMID: 31251078
Although no sex*APOE genotype interactions were observed for SPMs expressed as a ratio of their parent compound, higher cortical 18R/S-hydroxy-5Z,8Z,11Z,14Z,16E-EPA, resolvin D3, protectin D1, 10S,17S-dihydroxy-4Z,7Z,11E,13E,15Z,19Z-DHA (10S,17S-diHDHA), mare …
Although no sex*APOE genotype interactions were observed for SPMs expressed as a ratio of their parent compound, higher cortical 18R/S-hydro …
Cytochrome P450-type hydroxylation and epoxidation in a tyrosine-liganded hemoprotein, catalase-related allene oxide synthase.
Boeglin WE, Brash AR. Boeglin WE, et al. J Biol Chem. 2012 Jul 13;287(29):24139-47. doi: 10.1074/jbc.M112.364216. Epub 2012 May 24. J Biol Chem. 2012. PMID: 22628547 Free PMC article.
Here we oxidized cAOS to Compound I (Fe(V)=O) using the oxygen donor iodosylbenzene and investigated the catalytic competence of the enzyme. 8R-hydroxyeicosatetraenoic acid (8R-HETE), the hydroxy analog of the natural substrate, normally unreactive with cAOS, was thereby epoxidiz …
Here we oxidized cAOS to Compound I (Fe(V)=O) using the oxygen donor iodosylbenzene and investigated the catalytic competence of the enzyme. …
Resolvins D1, D2, and other mediators of self-limited resolution of inflammation in human blood following n-3 fatty acid supplementation.
Mas E, Croft KD, Zahra P, Barden A, Mori TA. Mas E, et al. Clin Chem. 2012 Oct;58(10):1476-84. doi: 10.1373/clinchem.2012.190199. Epub 2012 Aug 21. Clin Chem. 2012. PMID: 22912397 Free article.
Plasma or serum was purified by solid-phase chromatography and analyzed with LC-MS/MS. RESULTS: The assay identified 18R/S-hydroxy-5Z,8Z,11Z,14Z,16E-eicosapentaenoic acid (18R/S-HEPE); 17S-hydroxy-4Z,7Z,10Z,13Z,15E,19Z-docosahexaenoic acid (17R/S-HDHA); 7S,8R,17S-trihydrox …
Plasma or serum was purified by solid-phase chromatography and analyzed with LC-MS/MS. RESULTS: The assay identified 18R/S-hydroxy-5Z