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Showing 1 to 12 of 13 entries
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General Synthetic Method for Si-Fluoresceins and Si-Rhodamines.

ACS central science

Grimm JB, Brown TA, Tkachuk AN, Lavis LD.
PMID: 28979939
ACS Cent Sci. 2017 Sep 27;3(9):975-985. doi: 10.1021/acscentsci.7b00247. Epub 2017 Aug 09.

The century-old fluoresceins and rhodamines persist as flexible scaffolds for fluorescent and fluorogenic compounds. Extensive exploration of these xanthene dyes has yielded general structure-activity relationships where the development of new probes is limited only by imagination and organic chemistry....

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Grimm JB, Brown TA, Tkachuk AN, et al. General Synthetic Method for Si-Fluoresceins and Si-Rhodamines. ACS Cent Sci. 2017;3(9):975-985doi: 10.1021/acscentsci.7b00247.
Grimm, J. B., Brown, T. A., Tkachuk, A. N., & Lavis, L. D. (2017). General Synthetic Method for Si-Fluoresceins and Si-Rhodamines. ACS central science, 3(9), 975-985. https://doi.org/10.1021/acscentsci.7b00247
Grimm, Jonathan B, et al. "General Synthetic Method for Si-Fluoresceins and Si-Rhodamines." ACS central science vol. 3,9 (2017): 975-985. doi: https://doi.org/10.1021/acscentsci.7b00247
Grimm JB, Brown TA, Tkachuk AN, Lavis LD. General Synthetic Method for Si-Fluoresceins and Si-Rhodamines. ACS Cent Sci. 2017 Sep 27;3(9):975-985. doi: 10.1021/acscentsci.7b00247. Epub 2017 Aug 09. PMID: 28979939; PMCID: PMC5620978.
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Near-infrared fluorescein dyes containing a tricoordinate boron atom.

Chemical science

Ando N, Soutome H, Yamaguchi S.
PMID: 31588332
Chem Sci. 2019 Jul 03;10(33):7816-7821. doi: 10.1039/c9sc02314c. eCollection 2019 Sep 07.

Bora-fluoresceins (

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Ando N, Soutome H, Yamaguchi S. Near-infrared fluorescein dyes containing a tricoordinate boron atom. Chem Sci. 2019;10(33):7816-7821doi: 10.1039/c9sc02314c.
Ando, N., Soutome, H., & Yamaguchi, S. (2019). Near-infrared fluorescein dyes containing a tricoordinate boron atom. Chemical science, 10(33), 7816-7821. https://doi.org/10.1039/c9sc02314c
Ando, Naoki, et al. "Near-infrared fluorescein dyes containing a tricoordinate boron atom." Chemical science vol. 10,33 (2019): 7816-7821. doi: https://doi.org/10.1039/c9sc02314c
Ando N, Soutome H, Yamaguchi S. Near-infrared fluorescein dyes containing a tricoordinate boron atom. Chem Sci. 2019 Jul 03;10(33):7816-7821. doi: 10.1039/c9sc02314c. eCollection 2019 Sep 07. PMID: 31588332; PMCID: PMC6764465.
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Photostability and spectral properties of fluorinated fluoresceins and their biarsenical derivatives: a combined experimental and theoretical study.

Photochemistry and photobiology

Spagnuolo CC, Massad W, Miskoski S, Menendez GO, García NA, Jares-Erijman EA.
PMID: 19500295
Photochem Photobiol. 2009 Sep-Oct;85(5):1082-8. doi: 10.1111/j.1751-1097.2009.00565.x. Epub 2009 May 20.

New fluorinated biarsenical derivatives with improved optical properties based on highly photostable analogs of fluorescein were recently introduced. The photophysical parameters of the triplet excited states as well as photosensitized oxidation reactions of these dyes were determined in order...

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Spagnuolo CC, Massad W, Miskoski S, et al. Photostability and spectral properties of fluorinated fluoresceins and their biarsenical derivatives: a combined experimental and theoretical study. Photochem Photobiol. 2009;85(5):1082-8doi: 10.1111/j.1751-1097.2009.00565.x.
Spagnuolo, C. C., Massad, W., Miskoski, S., Menendez, G. O., García, N. A., & Jares-Erijman, E. A. (2009). Photostability and spectral properties of fluorinated fluoresceins and their biarsenical derivatives: a combined experimental and theoretical study. Photochemistry and photobiology, 85(5), 1082-8. https://doi.org/10.1111/j.1751-1097.2009.00565.x
Spagnuolo, Carla C, et al. "Photostability and spectral properties of fluorinated fluoresceins and their biarsenical derivatives: a combined experimental and theoretical study." Photochemistry and photobiology vol. 85,5 (2009): 1082-8. doi: https://doi.org/10.1111/j.1751-1097.2009.00565.x
Spagnuolo CC, Massad W, Miskoski S, Menendez GO, García NA, Jares-Erijman EA. Photostability and spectral properties of fluorinated fluoresceins and their biarsenical derivatives: a combined experimental and theoretical study. Photochem Photobiol. 2009 Sep-Oct;85(5):1082-8. doi: 10.1111/j.1751-1097.2009.00565.x. Epub 2009 May 20. PMID: 19500295.
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Studies on fluorescein-II The solubility and acid dissociation constants of fluorescein in water solution.

Talanta

Diehl H, Markuszewski R.
PMID: 18963816
Talanta. 1985 Feb;32(2):159-65. doi: 10.1016/0039-9140(85)80049-7.

The solubility of yellow fluorescein and of red fluorescein as a function of pH has been measured in water at ionic strength 0.10. The pH of minimum solubility is the same for both, 3.28. The intrinsic solubility, defined as...

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Diehl H, Markuszewski R. Studies on fluorescein-II The solubility and acid dissociation constants of fluorescein in water solution. Talanta. 1985;32(2):159-65doi: 10.1016/0039-9140(85)80049-7.
Diehl, H., & Markuszewski, R. (1985). Studies on fluorescein-II The solubility and acid dissociation constants of fluorescein in water solution. Talanta, 32(2), 159-65. https://doi.org/10.1016/0039-9140(85)80049-7
Diehl, H, and Markuszewski, R. "Studies on fluorescein-II The solubility and acid dissociation constants of fluorescein in water solution." Talanta vol. 32,2 (1985): 159-65. doi: https://doi.org/10.1016/0039-9140(85)80049-7
Diehl H, Markuszewski R. Studies on fluorescein-II The solubility and acid dissociation constants of fluorescein in water solution. Talanta. 1985 Feb;32(2):159-65. doi: 10.1016/0039-9140(85)80049-7. PMID: 18963816.
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Photoinitiated Free-Radical Polymerization of 4,5,6,7-Tetrahalogenated Fluoresceins.

Chemistry, an Asian journal

Jung YJ, Nganga JB, Cho JH, Lee HI, Lee JK.
PMID: 34213840
Chem Asian J. 2021 Sep 01;16(17):2413-2416. doi: 10.1002/asia.202100619. Epub 2021 Jul 16.

We demonstrated the photoredox catalytic performances of fluorescein derivatives, bearing heavy halogen atoms (Br or I) on a benzoic acid group, using photoinitiated free-radical polymerization. 4,5,6,7-Tetrabromofluorescein and 4,5,6,7-tetraiodofluorescein were used as visible-light-photoredox catalysts to initiate polymerization of poly(ethylene glycol)...

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Jung YJ, Nganga JB, Cho JH, et al. Photoinitiated Free-Radical Polymerization of 4,5,6,7-Tetrahalogenated Fluoresceins. Chem Asian J. 2021;16(17):2413-2416doi: 10.1002/asia.202100619.
Jung, Y. J., Nganga, J. B., Cho, J. H., Lee, H. I., & Lee, J. K. (2021). Photoinitiated Free-Radical Polymerization of 4,5,6,7-Tetrahalogenated Fluoresceins. Chemistry, an Asian journal, 16(17), 2413-2416. https://doi.org/10.1002/asia.202100619
Jung, Young Jae, et al. "Photoinitiated Free-Radical Polymerization of 4,5,6,7-Tetrahalogenated Fluoresceins." Chemistry, an Asian journal vol. 16,17 (2021): 2413-2416. doi: https://doi.org/10.1002/asia.202100619
Jung YJ, Nganga JB, Cho JH, Lee HI, Lee JK. Photoinitiated Free-Radical Polymerization of 4,5,6,7-Tetrahalogenated Fluoresceins. Chem Asian J. 2021 Sep 01;16(17):2413-2416. doi: 10.1002/asia.202100619. Epub 2021 Jul 16. PMID: 34213840.
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Auxin transport inhibitors: fluorescein and related compounds.

Plant physiology

Katekar GF, Geissler AE.
PMID: 16659362
Plant Physiol. 1975 Nov;56(5):645-6. doi: 10.1104/pp.56.5.645.

Fluoresceins are shown to be effective inhibitors of indoleacetic acid transport as measured by the receiver agar block technique, eosin having the same order of activity as 2,3,5-triiodobenzoic acid and N-1-naphthylphthalamic acid, with fluorescein less effective. It is suggested...

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Katekar GF, Geissler AE. Auxin transport inhibitors: fluorescein and related compounds. Plant Physiol. 1975;56(5):645-6doi: 10.1104/pp.56.5.645.
Katekar, G. F., & Geissler, A. E. (1975). Auxin transport inhibitors: fluorescein and related compounds. Plant physiology, 56(5), 645-6. https://doi.org/10.1104/pp.56.5.645
Katekar, G F, and Geissler, A E. "Auxin transport inhibitors: fluorescein and related compounds." Plant physiology vol. 56,5 (1975): 645-6. doi: https://doi.org/10.1104/pp.56.5.645
Katekar GF, Geissler AE. Auxin transport inhibitors: fluorescein and related compounds. Plant Physiol. 1975 Nov;56(5):645-6. doi: 10.1104/pp.56.5.645. PMID: 16659362; PMCID: PMC541889.
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Specific protein labeling with caged fluorophores for dual-color imaging and super-resolution microscopy in living cells.

Chemical science

Hauke S, von Appen A, Quidwai T, Ries J, Wombacher R.
PMID: 28451202
Chem Sci. 2017 Jan 01;8(1):559-566. doi: 10.1039/c6sc02088g. Epub 2016 Sep 05.

We present new fluorophore-conjugates for dual-color photoactivation and super-resolution imaging inside live mammalian cells. These custom-designed, photo-caged Q-rhodamines and fluoresceins are cell-permeable, bright and localize specifically to intracellular targets. We utilized established orthogonal protein labeling strategies to precisely attach...

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Hauke S, von Appen A, Quidwai T, et al. Specific protein labeling with caged fluorophores for dual-color imaging and super-resolution microscopy in living cells. Chem Sci. 2016;8(1):559-566doi: 10.1039/c6sc02088g.
Hauke, S., von Appen, A., Quidwai, T., Ries, J., & Wombacher, R. (2017). Specific protein labeling with caged fluorophores for dual-color imaging and super-resolution microscopy in living cells. Chemical science, 8(1), 559-566. https://doi.org/10.1039/c6sc02088g
Hauke, Sebastian, et al. "Specific protein labeling with caged fluorophores for dual-color imaging and super-resolution microscopy in living cells." Chemical science vol. 8,1 (2017): 559-566. doi: https://doi.org/10.1039/c6sc02088g
Hauke S, von Appen A, Quidwai T, Ries J, Wombacher R. Specific protein labeling with caged fluorophores for dual-color imaging and super-resolution microscopy in living cells. Chem Sci. 2017 Jan 01;8(1):559-566. doi: 10.1039/c6sc02088g. Epub 2016 Sep 05. PMID: 28451202; PMCID: PMC5351804.
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Balanced Intersystem Crossing in Iodinated Silicon-Fluoresceins Allows New Class of Red Shifted Theranostic Agents.

ACS medicinal chemistry letters

Cetin S, Elmazoglu Z, Karaman O, Gunduz H, Gunbas G, Kolemen S.
PMID: 34055222
ACS Med Chem Lett. 2021 Mar 16;12(5):752-757. doi: 10.1021/acsmedchemlett.1c00018. eCollection 2021 May 13.

Iodination of the silicon-fluorescein core revealed a new class of highly cytotoxic, red-shifted and water-soluble photosensitizer (SF-I) which is also fairly emissive to serve as a theranostic agent. Singlet oxygen generation capacity of SF-I was evaluated chemically, and up...

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Cetin S, Elmazoglu Z, Karaman O, et al. Balanced Intersystem Crossing in Iodinated Silicon-Fluoresceins Allows New Class of Red Shifted Theranostic Agents. ACS Med Chem Lett. 2021;12(5):752-757doi: 10.1021/acsmedchemlett.1c00018.
Cetin, S., Elmazoglu, Z., Karaman, O., Gunduz, H., Gunbas, G., & Kolemen, S. (2021). Balanced Intersystem Crossing in Iodinated Silicon-Fluoresceins Allows New Class of Red Shifted Theranostic Agents. ACS medicinal chemistry letters, 12(5), 752-757. https://doi.org/10.1021/acsmedchemlett.1c00018
Cetin, Sultan, et al. "Balanced Intersystem Crossing in Iodinated Silicon-Fluoresceins Allows New Class of Red Shifted Theranostic Agents." ACS medicinal chemistry letters vol. 12,5 (2021): 752-757. doi: https://doi.org/10.1021/acsmedchemlett.1c00018
Cetin S, Elmazoglu Z, Karaman O, Gunduz H, Gunbas G, Kolemen S. Balanced Intersystem Crossing in Iodinated Silicon-Fluoresceins Allows New Class of Red Shifted Theranostic Agents. ACS Med Chem Lett. 2021 Mar 16;12(5):752-757. doi: 10.1021/acsmedchemlett.1c00018. eCollection 2021 May 13. PMID: 34055222; PMCID: PMC8155232.
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Mild synthesis of asymmetric 2'-carboxyethyl-substituted fluoresceins.

The Journal of organic chemistry

Lukhtanov EA, Vorobiev AV.
PMID: 18302409
J Org Chem. 2008 Mar 21;73(6):2424-7. doi: 10.1021/jo702422v. Epub 2008 Feb 27.

Asymmetric fluoresceins bearing a carboxyethyl group in the chromophoric portion of the dyes were prepared by a reaction of substituted phthalic anhydride with a carboxyethyl substituted resorcinol analogue followed by a condensation with a second resorcinol analogue. In order...

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Lukhtanov EA, Vorobiev AV. Mild synthesis of asymmetric 2'-carboxyethyl-substituted fluoresceins. J Org Chem. 2008;73(6):2424-7doi: 10.1021/jo702422v.
Lukhtanov, E. A., & Vorobiev, A. V. (2008). Mild synthesis of asymmetric 2'-carboxyethyl-substituted fluoresceins. The Journal of organic chemistry, 73(6), 2424-7. https://doi.org/10.1021/jo702422v
Lukhtanov, Eugeny A, and Vorobiev, Alexei V. "Mild synthesis of asymmetric 2'-carboxyethyl-substituted fluoresceins." The Journal of organic chemistry vol. 73,6 (2008): 2424-7. doi: https://doi.org/10.1021/jo702422v
Lukhtanov EA, Vorobiev AV. Mild synthesis of asymmetric 2'-carboxyethyl-substituted fluoresceins. J Org Chem. 2008 Mar 21;73(6):2424-7. doi: 10.1021/jo702422v. Epub 2008 Feb 27. PMID: 18302409.
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In Vivo Nerve-Specificity of Rhodamines and Si-rhodamines.

Proceedings of SPIE--the International Society for Optical Engineering

Montaño AR, Wang LG, Barth CW, Shams NA, Kumarapeli KASU, Gibbs SL.
PMID: 32255888
Proc SPIE Int Soc Opt Eng. 2020 Feb;11222. doi: 10.1117/12.2545311. Epub 2020 Feb 19.

Accidental nerve damage or transection of vital nerve structures remains an unfortunate reality that is often associated with surgery. Despite the existence of nerve-sparing techniques, the success of such procedures is not only complicated by anatomical variance across patients...

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Montaño AR, Wang LG, Barth CW, et al. In Vivo Nerve-Specificity of Rhodamines and Si-rhodamines. Proc SPIE Int Soc Opt Eng. 2020;11222doi: 10.1117/12.2545311.
Montaño, A. R., Wang, L. G., Barth, C. W., Shams, N. A., Kumarapeli, K. A. S. U., & Gibbs, S. L. (2020). In Vivo Nerve-Specificity of Rhodamines and Si-rhodamines. Proceedings of SPIE--the International Society for Optical Engineering, 11222. https://doi.org/10.1117/12.2545311
Montaño, Antonio R, et al. "In Vivo Nerve-Specificity of Rhodamines and Si-rhodamines." Proceedings of SPIE--the International Society for Optical Engineering vol. 11222 (2020). doi: https://doi.org/10.1117/12.2545311
Montaño AR, Wang LG, Barth CW, Shams NA, Kumarapeli KASU, Gibbs SL. In Vivo Nerve-Specificity of Rhodamines and Si-rhodamines. Proc SPIE Int Soc Opt Eng. 2020 Feb;11222. doi: 10.1117/12.2545311. Epub 2020 Feb 19. PMID: 32255888; PMCID: PMC7115044.
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A Cu(II) Indicator Platform Based on Cu(II) Induced Swelling that Changes the Extent of Fluorescein Self-Quenching.

Polymers

Wang F, Planalp RP, Seitz WR.
PMID: 31775268
Polymers (Basel). 2019 Nov 25;11(12). doi: 10.3390/polym11121935.

In this study, we established a new fluorescent indicator platform. The responsive element consists of poly(N-isopropylacrylamide) nanospheres that include small percentages of fluorescein and a ligand, anilinodiacetate (phenylIDA). Nanosphere diameters were determined to be in the range from 50...

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Wang F, Planalp RP, Seitz WR. A Cu(II) Indicator Platform Based on Cu(II) Induced Swelling that Changes the Extent of Fluorescein Self-Quenching. Polymers (Basel). 2019;11(12)doi: 10.3390/polym11121935.
Wang, F., Planalp, R. P., & Seitz, W. R. (2019). A Cu(II) Indicator Platform Based on Cu(II) Induced Swelling that Changes the Extent of Fluorescein Self-Quenching. Polymers, 11(12), . https://doi.org/10.3390/polym11121935
Wang, Feifei, et al. "A Cu(II) Indicator Platform Based on Cu(II) Induced Swelling that Changes the Extent of Fluorescein Self-Quenching." Polymers vol. 11,12 (2019). doi: https://doi.org/10.3390/polym11121935
Wang F, Planalp RP, Seitz WR. A Cu(II) Indicator Platform Based on Cu(II) Induced Swelling that Changes the Extent of Fluorescein Self-Quenching. Polymers (Basel). 2019 Nov 25;11(12). doi: 10.3390/polym11121935. PMID: 31775268; PMCID: PMC6960841.
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Selective Conversion of P=O-Bridged Rhodamines into P=O-Rhodols: Solvatochromic Near-Infrared Fluorophores.

Chemistry (Weinheim an der Bergstrasse, Germany)

Grzybowski M, Taki M, Yamaguchi S.
PMID: 28748577
Chemistry. 2017 Sep 21;23(53):13028-13032. doi: 10.1002/chem.201703456. Epub 2017 Aug 22.

The substitution of an oxygen atom in rhodols with a phosphine oxide (P=O) moiety affords P=O-bridged rhodols as a new type of near-infrared (NIR) fluorophore. This compound class can be readily accessed upon exposure of the corresponding rhodamines to...

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Grzybowski M, Taki M, Yamaguchi S. Selective Conversion of P=O-Bridged Rhodamines into P=O-Rhodols: Solvatochromic Near-Infrared Fluorophores. Chemistry. 2017;23(53):13028-13032doi: 10.1002/chem.201703456.
Grzybowski, M., Taki, M., & Yamaguchi, S. (2017). Selective Conversion of P=O-Bridged Rhodamines into P=O-Rhodols: Solvatochromic Near-Infrared Fluorophores. Chemistry (Weinheim an der Bergstrasse, Germany), 23(53), 13028-13032. https://doi.org/10.1002/chem.201703456
Grzybowski, Marek, et al. "Selective Conversion of P=O-Bridged Rhodamines into P=O-Rhodols: Solvatochromic Near-Infrared Fluorophores." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 23,53 (2017): 13028-13032. doi: https://doi.org/10.1002/chem.201703456
Grzybowski M, Taki M, Yamaguchi S. Selective Conversion of P=O-Bridged Rhodamines into P=O-Rhodols: Solvatochromic Near-Infrared Fluorophores. Chemistry. 2017 Sep 21;23(53):13028-13032. doi: 10.1002/chem.201703456. Epub 2017 Aug 22. PMID: 28748577.
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Showing 1 to 12 of 13 entries