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Quoted phrases not found in phrase index: "1,5-dihydroxyanthracene-9,10-dione", "anthrarufine"
Page 1
Sulfonated Poly(2,6-dimethyl-1,4-phenylene ether)-Modified Mixed-Matrix Bifunctional Polyelectrolyte Membranes for Long-Run Anthrarufin-Based Redox Flow Batteries.
Sharma J, Gupta R, Mishra S, Ramanujam K, Kulshrestha V. Sharma J, et al. ACS Appl Mater Interfaces. 2023 Sep 27;15(38):44899-44911. doi: 10.1021/acsami.3c08089. Epub 2023 Sep 14. ACS Appl Mater Interfaces. 2023. PMID: 37708403
Herein, we report on studies corroborating the synergistic influence of ionic domain microstructure modification and intercalation of telechelic bis-piperidinium-functionalized graphene oxide (GO) to fabricate stable bifunctional membranes from sulfonated poly(2,6-dimethyl-1,4-ph …
Herein, we report on studies corroborating the synergistic influence of ionic domain microstructure modification and intercalation of telech …
Biosynthesis of Rhamnosylated Anthraquinones in Escherichia coli.
Nguyen TTH, Sin HJ, Pandey RP, Jung HJ, Liou K, Sohng JK. Nguyen TTH, et al. J Microbiol Biotechnol. 2020 Mar 28;30(3):398-403. doi: 10.4014/jmb.1911.11047. J Microbiol Biotechnol. 2020. PMID: 31893599 Free PMC article.
Among the five anthraquinones (alizarin, emodin, chrysazin, anthrarufin, and quinizarin) tested, quinizarin was biotransformed into a rhamoside derivative with the highest conversion ratio by whole cells of engineered E. coli. ...
Among the five anthraquinones (alizarin, emodin, chrysazin, anthrarufin, and quinizarin) tested, quinizarin was biotransformed into a …
Electrocoagulation of quinone pigments.
Chairungsi N, Jumpatong K, Suebsakwong P, Sengpracha W, Phutdhawong W, Buddhasukh D. Chairungsi N, et al. Molecules. 2006 Jul 14;11(7):514-22. doi: 10.3390/11070514. Molecules. 2006. PMID: 17971722 Free PMC article.
Some representative quinones, viz. one naphthoquinone (plumbagin) and five anthraquinones (alizarin, purpurin, chrysazin, emodin, and anthrarufin), were subjected to electrocoagulation. It was found that the rate and extent of coagulation of these compounds appears to corr …
Some representative quinones, viz. one naphthoquinone (plumbagin) and five anthraquinones (alizarin, purpurin, chrysazin, emodin, and ant
Bovine Serum Albumin Amplified Reactive Oxygen Species Generation from Anthrarufin-Derived Carbon Dot and Concomitant Nanoassembly for Combination Antibiotic-Photodynamic Therapy Application.
Mandal S, Prasad SR, Mandal D, Das P. Mandal S, et al. ACS Appl Mater Interfaces. 2019 Sep 11;11(36):33273-33284. doi: 10.1021/acsami.9b12455. Epub 2019 Aug 30. ACS Appl Mater Interfaces. 2019. PMID: 31433943
Derivatization of surface carboxyl functional groups of Anthrarufin-derived, green-emitting CD with the amine functionality of BSA ushers distinct changes in the photophysics of CD including an unprecedented 50 nm shift in its excitation maxima, decrease in fluorescence li …
Derivatization of surface carboxyl functional groups of Anthrarufin-derived, green-emitting CD with the amine functionality of BSA us …
The O/OREOS mission: first science data from the space environment viability of organics (SEVO) payload.
Mattioda A, Cook A, Ehrenfreund P, Quinn R, Ricco AJ, Squires D, Bramall N, Bryson K, Chittenden J, Minelli G, Agasid E, Allamandola L, Beasley C, Burton R, Defouw G, Diaz-Aguado M, Fonda M, Friedericks C, Kitts C, Landis D, McIntyre M, Neumann M, Rasay M, Ricks R, Salama F, Santos O, Schooley A, Yost B, Young A. Mattioda A, et al. Astrobiology. 2012 Sep;12(9):841-53. doi: 10.1089/ast.2012.0861. Astrobiology. 2012. PMID: 22984872
Spectra from the PAH thin film in a water-vapor-containing microenvironment indicate measurable change due to solar irradiation in orbit, while three other nominally water-free microenvironments show no appreciable change. The quinone anthrarufin showed high photostability …
Spectra from the PAH thin film in a water-vapor-containing microenvironment indicate measurable change due to solar irradiation in orbit, wh …
Carbon dot mediated G quadruplex nano-network formation for enhanced DNAzyme activity and easy catalyst reclamation.
Kumari S, Mandal S, Das P. Kumari S, et al. RSC Adv. 2019 Dec 17;9(71):41502-41510. doi: 10.1039/c9ra08290e. eCollection 2019 Dec 13. RSC Adv. 2019. PMID: 35541604 Free PMC article.
Herein, we report the creation of a network array of G-quadruplex (G4)-hemin complexes crosslinked by carbon quantum dots (CDs) that not only significantly improves the G-quadruplex-hemin DNAzyme activity, stability, and catalytic cycle, but also points towards easy catalyst rege …
Herein, we report the creation of a network array of G-quadruplex (G4)-hemin complexes crosslinked by carbon quantum dots (CDs) that not onl …
C-Aryl glycosides via tandem intramolecular benzyne-furan cycloadditions. Total synthesis of vineomycinone B2 methyl ester.
Chen CL, Sparks SM, Martin SF. Chen CL, et al. J Am Chem Soc. 2006 Oct 25;128(42):13696-7. doi: 10.1021/ja0652619. J Am Chem Soc. 2006. PMID: 17044691 Free PMC article.
The synthesis features the use of silicon tethers as disposable linkers to control the regiochemistry in two tandem Diels-Alder reactions of substituted benzynes and glycosyl furans to provide rapid access to the fully intact anthrarufin core of vineomycinone B2 methyl est …
The synthesis features the use of silicon tethers as disposable linkers to control the regiochemistry in two tandem Diels-Alder reactions of …
Naphthoquinones and anthraquinones: Exploring their impact on acetylcholinesterase enzyme activity.
Duran HE, Beydemir Ş. Duran HE, et al. Biotechnol Appl Biochem. 2024 Oct;71(5):1079-1093. doi: 10.1002/bab.2599. Epub 2024 May 7. Biotechnol Appl Biochem. 2024. PMID: 38715453
Furthermore, because it had the lowest K(I) value of any of these substances, 1,5-dihydroxyanthraquinone (1c) was shown to be the most potent inhibitor. The findings will add to the body of knowledge on the creation of fresh, potent, and successful treatment …
Furthermore, because it had the lowest K(I) value of any of these substances, 1,5-dihydroxyanthraquinone (1c) was shown …
Two-dimensional confinement for generating thin single crystals for applications in time-resolved electron diffraction and spectroscopy: an intramolecular proton transfer study.
Hwang H, Tiwari V, Duan HG, Bittmann SF, Tellkamp F, Jha A, Miller RJD. Hwang H, et al. Chem Commun (Camb). 2022 Aug 30;58(70):9774-9777. doi: 10.1039/d2cc02468c. Chem Commun (Camb). 2022. PMID: 35968881
Here, we present a general method based on spatial confinement to grow such crystals using the prototypical proton transfer system, 1,5-dihydroxyanthraquinone, as an example, and provide the protocol for optically characterizing structural dynamics to enable …
Here, we present a general method based on spatial confinement to grow such crystals using the prototypical proton transfer system, 1
32 results