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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1965 1
1978 1
1979 2
1981 1
1982 1
1989 1
1991 1
1998 1
2000 1
2001 1
2005 1
2009 1
2015 1
2021 1
2022 1
2024 0

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16 results

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Page 1
2,5-Diphenylfuran-based pure antiestrogens with selectivity for the estrogen receptor alpha.
Zimmermann J, Liebl R, von Angerer E. Zimmermann J, et al. J Steroid Biochem Mol Biol. 2005 Feb;94(1-3):57-66. doi: 10.1016/j.jsbmb.2004.12.018. Epub 2005 Feb 24. J Steroid Biochem Mol Biol. 2005. PMID: 15862950
Several chemical structures with selective binding affinity for ERalpha have been identified and might be useful for the synthesis of ERalpha-selective pure antiestrogens. In this study we applied the 2,5-diphenylfuran system which is closely related to the t …
Several chemical structures with selective binding affinity for ERalpha have been identified and might be useful for the synthesis of ERalph …
Spectroscopic (FT-IR, (1)H, (13)C NMR and UV-vis) characterization and DFT studies of novel 8-((4-(methylthio)-2,5-diphenylfuran-3-yl)methoxy)quinoline.
Diwaker, Chidan Kumar CS, Kumar A, Chandraju S. Diwaker, et al. Spectrochim Acta A Mol Biomol Spectrosc. 2015 Nov 5;150:602-13. doi: 10.1016/j.saa.2015.06.003. Epub 2015 Jun 10. Spectrochim Acta A Mol Biomol Spectrosc. 2015. PMID: 26079516
In this study, computational calculations of a new quinoline derivative: 8-((4-(methylthio)-2,5-diphenylfuran-3-yl)methoxy)quinoline is carried out using ab initio methods. ...
In this study, computational calculations of a new quinoline derivative: 8-((4-(methylthio)-2,5-diphenylfuran-3-yl)meth …
Lifetime broadening in the rotationally resolved electronic spectra of dibenzothiophene, 2,5-diphenylfuran, and 2,5-diphenyl-1,3,4-oxadiazole in the gas phase. Intersystem crossing dynamics in the statistical limit.
Alvarez-Valtierra L, Yi JT, Pratt DW. Alvarez-Valtierra L, et al. J Phys Chem A. 2009 Mar 19;113(11):2261-7. doi: 10.1021/jp807397t. J Phys Chem A. 2009. PMID: 19220022
Two other heterocyclic molecules manifest similar photophysical properties; 2,5-diphenylfuran and 2,5-diphenyl-1,3,4-oxadiazole. Lorentzian line shape broadenings of approximately 76 MHz were observed in the high-resolution spectra of their origin bands. ...
Two other heterocyclic molecules manifest similar photophysical properties; 2,5-diphenylfuran and 2,5-diphenyl-1,3,4-ox …
NOTE ON DERIVATIVES OF 2,5-DIPHENYLFURAN.
BAVIN PM. BAVIN PM. J Pharm Pharmacol. 1965 Apr;17:236-8. doi: 10.1111/j.2042-7158.1965.tb07651.x. J Pharm Pharmacol. 1965. PMID: 14327712 No abstract available.
Approaching the Spin-Statistical Limit in Visible-to-Ultraviolet Photon Upconversion.
Olesund A, Johnsson J, Edhborg F, Ghasemi S, Moth-Poulsen K, Albinsson B. Olesund A, et al. J Am Chem Soc. 2022 Mar 2;144(8):3706-3716. doi: 10.1021/jacs.1c13222. Epub 2022 Feb 17. J Am Chem Soc. 2022. PMID: 35175751 Free PMC article.
We report a record-setting internal TTA-UC quantum yield (phi(UC,g)) of 16.8% (out of a 50% maximum) for 1,4-bis((triisopropylsilyl)ethynyl)naphthalene, demonstrating the first example of a visible-to-UV TTA-UC system approaching the classical spin-statistical limit of 20%. Three …
We report a record-setting internal TTA-UC quantum yield (phi(UC,g)) of 16.8% (out of a 50% maximum) for 1,4-bis((triisopropylsilyl)ethynyl) …
Diguanidino and "reversed" diamidino 2,5-diarylfurans as antimicrobial agents.
Stephens CE, Tanious F, Kim S, Wilson WD, Schell WA, Perfect JR, Franzblau SG, Boykin DW. Stephens CE, et al. J Med Chem. 2001 May 24;44(11):1741-8. doi: 10.1021/jm000413a. J Med Chem. 2001. PMID: 11356109
The binding affinities are highly dependent on structure and are significantly affected by substituents both on the phenyl rings of the 2,5-diphenylfuran nucleus and on the cationic centers. Of the 17 novel dicationic compounds synthesized, six (6a, 6b, 5b, 6 …
The binding affinities are highly dependent on structure and are significantly affected by substituents both on the phenyl rings of the 2 …
Studies on the properties of the singlet oxygen-like factor produced during lipid peroxidation.
Lai EK, Fong KL, McCay PB. Lai EK, et al. Biochim Biophys Acta. 1978 Mar 30;528(3):497-506. doi: 10.1016/0005-2760(78)90040-1. Biochim Biophys Acta. 1978. PMID: 638171
We now wish to report that purified fatty acid hydroperoxide alone, as well as peroxidized microsomal lipid and cumene hydroperoxide also form the singlet oxygen reaction product with 2,5-diphenylfuran. The reaction product (cis-1,2-dibenzoylethylene) was obs …
We now wish to report that purified fatty acid hydroperoxide alone, as well as peroxidized microsomal lipid and cumene hydroperoxide also fo …
The action of lipoxygenase-1 on furan derivatives.
Boyer RF, Litts D, Kostishak J, Wijesundera RC, Gunstone FD. Boyer RF, et al. Chem Phys Lipids. 1979 Nov;25(3):237-46. doi: 10.1016/0009-3084(79)90109-9. Chem Phys Lipids. 1979. PMID: 119581
Apparently furan IV is able to interact with an active site of lipoxygenase (Km = 220 microM). 2,5-Dimethylfuran (I), 2,5-diphenylfuran (II) and 3-(5'-methyl-2'-furyl)propenoic acid (III) were neither substrates nor inhibitors of lipoxygenase activity. ...
Apparently furan IV is able to interact with an active site of lipoxygenase (Km = 220 microM). 2,5-Dimethylfuran (I), 2,5-d …
Bactericidal activity of a superoxide anion-generating system. A model for the polymorphonuclear leukocyte.
Rosen H, Klebanoff SJ. Rosen H, et al. J Exp Med. 1979 Jan 1;149(1):27-39. doi: 10.1084/jem.149.1.27. J Exp Med. 1979. PMID: 216766 Free PMC article.
Carotenoid pigments are potent 1O2 quenchers. The xanthine oxidase system catalyzes the conversion of 2,5-diphenylfuran to cis-dibenzoylethylene, a reaction which can occur by a 1O2 mechanism. ...
Carotenoid pigments are potent 1O2 quenchers. The xanthine oxidase system catalyzes the conversion of 2,5-diphenylfuran …
16 results