Zeitschriftenartikel zum Thema „Fluorogenic dyes“
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Pham, Ha H., Christopher Szent-Gyorgyi, Wendy L. Brotherton, Brigitte F. Schmidt, Kimberly J. Zanotti, Alan S. Waggoner und Bruce A. Armitage. „Bichromophoric dyes for wavelength shifting of dye-protein fluoromodules“. Organic & Biomolecular Chemistry 13, Nr. 12 (2015): 3699–710. http://dx.doi.org/10.1039/c4ob02522a.
Martin, Annabell, und Pablo Rivera Fuentes. „A Baldwin-favored Cyclization Inspires the Development of Fluorogenic Polymethine Dyes for Bioimaging“. CHIMIA 78, Nr. 4 (24.04.2024): 196–99. http://dx.doi.org/10.2533/chimia.2024.196.
Mamaeva, Anastasiya A., Vladimir I. Martynov, Sergey M. Deyev und Alexey A. Pakhomov. „Comparison of Colorimetric and Fluorometric Chemosensors for Protein Concentration Determination and Approaches for Estimation of Their Limits of Detection“. Chemosensors 10, Nr. 12 (17.12.2022): 542. http://dx.doi.org/10.3390/chemosensors10120542.
Krell, Katja, und Hans-Achim Wagenknecht. „Fluorogenic and Bioorthogonal Modification of RNA Using Photoclick Chemistry“. Biomolecules 10, Nr. 3 (21.03.2020): 480. http://dx.doi.org/10.3390/biom10030480.
Martin, Annabell, und Pablo Rivera-Fuentes. „Fluorogenic polymethine dyes by intramolecular cyclization“. Current Opinion in Chemical Biology 80 (Juni 2024): 102444. http://dx.doi.org/10.1016/j.cbpa.2024.102444.
Li, Chenge, Marie-Aude Plamont, Hanna L. Sladitschek, Vanessa Rodrigues, Isabelle Aujard, Pierre Neveu, Thomas Le Saux, Ludovic Jullien und Arnaud Gautier. „Dynamic multicolor protein labeling in living cells“. Chemical Science 8, Nr. 8 (2017): 5598–605. http://dx.doi.org/10.1039/c7sc01364g.
Bruchez, Marcel P. „Dark dyes–bright complexes: fluorogenic protein labeling“. Current Opinion in Chemical Biology 27 (August 2015): 18–23. http://dx.doi.org/10.1016/j.cbpa.2015.05.014.
Qi, Jianjun, und Ching-Hsuan Tung. „Development of benzothiazole ‘click-on’ fluorogenic dyes“. Bioorganic & Medicinal Chemistry Letters 21, Nr. 1 (Januar 2011): 320–23. http://dx.doi.org/10.1016/j.bmcl.2010.11.009.
Gu, Lingyue, Kévin Renault, Anthony Romieu, Jean-Alexandre Richard und Rajavel Srinivasan. „Synthesis and spectral properties of 6′-triazolyl-dihydroxanthene-hemicyanine fused near-infrared dyes“. New Journal of Chemistry 44, Nr. 28 (2020): 12208–15. http://dx.doi.org/10.1039/d0nj01724h.
Karpenko, Iuliia A., Yosuke Niko, Viktor P. Yakubovskyi, Andriy O. Gerasov, Dominique Bonnet, Yuriy P. Kovtun und Andrey S. Klymchenko. „Push–pull dioxaborine as fluorescent molecular rotor: far-red fluorogenic probe for ligand–receptor interactions“. Journal of Materials Chemistry C 4, Nr. 14 (2016): 3002–9. http://dx.doi.org/10.1039/c5tc03411f.
Wang, Xiaoqing, Qingsong Liu, Fen Qi, Lin Li, Hai-Dong Yu, Zhipeng Liu und Wei Huang. „Benzothiazole–pyrimidine-based BODIPY analogues: promising luminophores with fluorescence sensing and imaging ability and asymmetrization-induced solid-state emission“. Dalton Transactions 45, Nr. 43 (2016): 17274–80. http://dx.doi.org/10.1039/c6dt03469a.
Kormos, Attila, Alexandra Egyed, Jasmine M. Olvany, Ágnes Szatmári, Adrienn Biró, Zsóka Csorba, Péter Kele und Krisztina Németh. „A Bioorthogonal Double Fluorogenic Probe to Visualize Protein–DNA Interaction“. Chemosensors 10, Nr. 1 (17.01.2022): 37. http://dx.doi.org/10.3390/chemosensors10010037.
Low, Michelle, Khin Yin Win, Enyi Ye, Shuhua Liu, Soon Huat Ng, Xiaoqun Zhou und Ming-Yong Han. „Fluorogenic Quantification of Albumin“. Australian Journal of Chemistry 67, Nr. 10 (2014): 1382. http://dx.doi.org/10.1071/ch14083.
Stensrud, Kenneth F., Kimberly J. Zanotti, Alan S. Waggoner und Bruce A. Armitage. „Spectral Properties of Fluorogenic Thiophene-derived Triarylmethane Dyes“. Photochemistry and Photobiology 95, Nr. 1 (23.11.2018): 406–10. http://dx.doi.org/10.1111/php.13037.
Liu, Pei, Vincent Grenier, Wootack Hong, Vikram R. Muller und Evan W. Miller. „Fluorogenic Targeting of Voltage-Sensitive Dyes to Neurons“. Journal of the American Chemical Society 139, Nr. 48 (20.11.2017): 17334–40. http://dx.doi.org/10.1021/jacs.7b07047.
Sokolov, A. I., A. A. Gorshkova, N. S. Baleeva und M. S. Baranov. „Keto-Analogs of Arylidene-Imidazolones as Fluorogenic Dyes“. Russian Journal of Bioorganic Chemistry 48, Nr. 6 (Dezember 2022): 1367–71. http://dx.doi.org/10.1134/s1068162022060243.
Bhasikuttan, Achikanath C., und Jyotirmayee Mohanty. „Targeting G-quadruplex structures with extrinsic fluorogenic dyes: promising fluorescence sensors“. Chemical Communications 51, Nr. 36 (2015): 7581–97. http://dx.doi.org/10.1039/c4cc10030a.
Vasilev, Aleksey A., Meglena I. Kandinska, Stanimir S. Stoyanov, Stanislava B. Yordanova, David Sucunza, Juan J. Vaquero, Obis D. Castaño, Stanislav Baluschev und Silvia E. Angelova. „Halogen-containing thiazole orange analogues – new fluorogenic DNA stains“. Beilstein Journal of Organic Chemistry 13 (28.12.2017): 2902–14. http://dx.doi.org/10.3762/bjoc.13.283.
Dou, Wei-Tao, Ying Lv, Chunyan Tan, Guo-Rong Chen und Xiao-Peng He. „Irreversible destruction of amyloid fibril plaques by conjugated polymer based fluorogenic nanogrenades“. Journal of Materials Chemistry B 4, Nr. 26 (2016): 4502–6. http://dx.doi.org/10.1039/c6tb01351a.
Alfindee, Madher N., Yagya P. Subedi, Michelle M. Grilley, Jon Y. Takemoto und Cheng-Wei T. Chang. „Antifungal Activities of 4″,6″-Disubstituted Amphiphilic Kanamycins“. Molecules 24, Nr. 10 (16.05.2019): 1882. http://dx.doi.org/10.3390/molecules24101882.
Diana, Rosita, Barbara Panunzi, Simona Concilio, Francesco Marrafino, Rafi Shikler, Tonino Caruso und Ugo Caruso. „The Effect of Bulky Substituents on Two π-Conjugated Mesogenic Fluorophores. Their Organic Polymers and Zinc-Bridged Luminescent Networks“. Polymers 11, Nr. 9 (22.08.2019): 1379. http://dx.doi.org/10.3390/polym11091379.
Smith, H. V., A. M. Grimason, C. Benton und J. F. W. Parker. „The Occurrence of Cryptosporidium Spp. Oocysts in Scottish Waters, and the Development of a Fluorogenic Viability Assay for Individual Cryptosporidium spp. Oocysts“. Water Science and Technology 24, Nr. 2 (01.07.1991): 169–72. http://dx.doi.org/10.2166/wst.1991.0051.
Silva, Gloria L., Volkan Ediz, David Yaron und Bruce A. Armitage. „Experimental and Computational Investigation of Unsymmetrical Cyanine Dyes: Understanding Torsionally Responsive Fluorogenic Dyes“. Journal of the American Chemical Society 129, Nr. 17 (Mai 2007): 5710–18. http://dx.doi.org/10.1021/ja070025z.
Qi, Jianjun, Myung-Shin Han, Yu-Cheng Chang und Ching-Hsuan Tung. „Developing Visible Fluorogenic ‘Click-On’ Dyes for Cellular Imaging“. Bioconjugate Chemistry 22, Nr. 9 (21.09.2011): 1758–62. http://dx.doi.org/10.1021/bc200282t.
Kisin-Finfer, Einat, und Doron Shabat. „New repertoire of ‘donor-two-acceptor’ NIR fluorogenic dyes“. Bioorganic & Medicinal Chemistry 21, Nr. 12 (Juni 2013): 3602–8. http://dx.doi.org/10.1016/j.bmc.2013.02.049.
Qi, Jianjun, und Ching-Hsuan Tung. „ChemInform Abstract: Development of Benzothiazole “Click-On” Fluorogenic Dyes.“ ChemInform 42, Nr. 20 (21.04.2011): no. http://dx.doi.org/10.1002/chin.201120179.
Vincent, Steve, Suman Mallick, Guillaume Barnoin, Hoang-Ngoan Le, Benoît Y. Michel und Alain Burger. „An Expeditious Approach towards the Synthesis and Application of Water-Soluble and Photostable Fluorogenic Chromones for DNA Detection“. Molecules 27, Nr. 7 (31.03.2022): 2267. http://dx.doi.org/10.3390/molecules27072267.
Yan, Qi, Brigitte F. Schmidt, Lydia A. Perkins, Matharishwan Naganbabu, Saumya Saurabh, Susan K. Andreko und Marcel P. Bruchez. „Near-instant surface-selective fluorogenic protein quantification using sulfonated triarylmethane dyes and fluorogen activating proteins“. Organic & Biomolecular Chemistry 13, Nr. 7 (2015): 2078–86. http://dx.doi.org/10.1039/c4ob02309a.
Debieu, Sylvain, und Anthony Romieu. „In situ formation of pyronin dyes for fluorescence protease sensing“. Organic & Biomolecular Chemistry 15, Nr. 12 (2017): 2575–84. http://dx.doi.org/10.1039/c7ob00370f.
Chi, Weijie, Lu Huang, Chao Wang, Davin Tan, Zhaochao Xu und Xiaogang Liu. „A unified fluorescence quenching mechanism of tetrazine-based fluorogenic dyes: energy transfer to a dark state“. Materials Chemistry Frontiers 5, Nr. 18 (2021): 7012–21. http://dx.doi.org/10.1039/d1qm00852h.
Ilieva, Sonia, Nadezhda Bozova, Miroslav Rangelov, Nadezhda Todorova, Aleksey Vasilev und Diana Cheshmedzhieva. „Asymmetric Monomethine Cyanine Dyes with Hydrophobic Functionalities for Fluorescent Intercalator Displacement Assay“. Molecules 29, Nr. 1 (23.12.2023): 114. http://dx.doi.org/10.3390/molecules29010114.
Constantin, Tudor P., Gloria L. Silva, Kelly L. Robertson, Tamara P. Hamilton, Kaitlin Fague, Alan S. Waggoner und Bruce A. Armitage. „Synthesis of New Fluorogenic Cyanine Dyes and Incorporation into RNA Fluoromodules“. Organic Letters 10, Nr. 8 (April 2008): 1561–64. http://dx.doi.org/10.1021/ol702920e.
Chauhan, Dinesh Pratapsinh, Tanmoy Saha, Mayurika Lahiri und Pinaki Talukdar. „BODIPY based ‘click on’ fluorogenic dyes: application in live cell imaging“. Tetrahedron Letters 55, Nr. 1 (Januar 2014): 244–47. http://dx.doi.org/10.1016/j.tetlet.2013.11.003.
O’Connor, Liam J., Ishna N. Mistry, Sarah L. Collins, Lisa K. Folkes, Graham Brown, Stuart J. Conway und Ester M. Hammond. „CYP450 Enzymes Effect Oxygen-Dependent Reduction of Azide-Based Fluorogenic Dyes“. ACS Central Science 3, Nr. 1 (19.12.2016): 20–30. http://dx.doi.org/10.1021/acscentsci.6b00276.
Zhang, Yuanwei, Xiling Yue, Bosung Kim, Sheng Yao, Mykhailo V. Bondar und Kevin D. Belfield. „Bovine Serum Albumin Nanoparticles with Fluorogenic Near-IR-Emitting Squaraine Dyes“. ACS Applied Materials & Interfaces 5, Nr. 17 (30.08.2013): 8710–17. http://dx.doi.org/10.1021/am402361w.
Ho, Nan-hui, Ralph Weissleder und Ching-Hsuan Tung. „Development of water-soluble far-red fluorogenic dyes for enzyme sensing“. Tetrahedron 62, Nr. 4 (Januar 2006): 578–85. http://dx.doi.org/10.1016/j.tet.2005.10.020.
NISHIZAWA, Seiichi, Yukina YOSHINO, Mengmeng HE, Kei HIGUCHI, Nao TOGASHI, Michiyuki SUZUKI, Yugo IGARASHI und Yusuke SATO. „Fluorogenic Monomethine Cyanine Dyes for Nucleolar RNA Imaging in Living Cells“. BUNSEKI KAGAKU 73, Nr. 3 (05.03.2024): 79–86. http://dx.doi.org/10.2116/bunsekikagaku.73.79.
Choi, Sang-Kee, Jonghoon Kim und Eunha Kim. „Overview of Syntheses and Molecular-Design Strategies for Tetrazine-Based Fluorogenic Probes“. Molecules 26, Nr. 7 (26.03.2021): 1868. http://dx.doi.org/10.3390/molecules26071868.
Zanotti, Kimberly J., Gloria L. Silva, Yehuda Creeger, Kelly L. Robertson, Alan S. Waggoner, Peter B. Berget und Bruce A. Armitage. „Blue fluorescent dye-protein complexes based on fluorogenic cyanine dyes and single chain antibody fragments“. Org. Biomol. Chem. 9, Nr. 4 (2011): 1012–20. http://dx.doi.org/10.1039/c0ob00444h.
Demeter, Orsolya, Attila Kormos, Christine Koehler, Gábor Mező, Krisztina Németh, Eszter Kozma, Levente B. Takács, Edward A. Lemke und Péter Kele. „Bisazide Cyanine Dyes as Fluorogenic Probes for Bis-Cyclooctynylated Peptide Tags and as Fluorogenic Cross-Linkers of Cyclooctynylated Proteins“. Bioconjugate Chemistry 28, Nr. 5 (28.04.2017): 1552–59. http://dx.doi.org/10.1021/acs.bioconjchem.7b00178.
Bozhanova, Nina, Mikhail Baranov, Nadezhda Baleeva, Alexey Gavrikov und Alexander Mishin. „Red-Shifted Aminated Derivatives of GFP Chromophore for Live-Cell Protein Labeling with Lipocalins“. International Journal of Molecular Sciences 19, Nr. 12 (28.11.2018): 3778. http://dx.doi.org/10.3390/ijms19123778.
Patalag, Lukas J., und Daniel B. Werz. „Benzothiadiazole oligoene fatty acids: fluorescent dyes with large Stokes shifts“. Beilstein Journal of Organic Chemistry 12 (14.12.2016): 2739–47. http://dx.doi.org/10.3762/bjoc.12.270.
Hannig, Christian, Marie Follo, Elmar Hellwig und Ali Al-Ahmad. „Visualization of adherent micro-organisms using different techniques“. Journal of Medical Microbiology 59, Nr. 1 (01.01.2010): 1–7. http://dx.doi.org/10.1099/jmm.0.015420-0.
Ediz, Volkan, Jihoon L. Lee, Bruce A. Armitage und David Yaron. „Molecular Engineering of Torsional Potentials in Fluorogenic Dyes via Electronic Substituent Effects“. Journal of Physical Chemistry A 112, Nr. 40 (09.10.2008): 9692–701. http://dx.doi.org/10.1021/jp805546s.
Klymchenko, Andrey S. „Solvatochromic and Fluorogenic Dyes as Environment-Sensitive Probes: Design and Biological Applications“. Accounts of Chemical Research 50, Nr. 2 (09.01.2017): 366–75. http://dx.doi.org/10.1021/acs.accounts.6b00517.
Chen, Lei, Fei Li, Mitoshi Nandi, Lu Huang, Zhizhong Chen, Junfa Wei, Weijie Chi, Xiaogang Liu und Jun Yang. „Towards tetrazine-based near-infrared fluorogenic dyes: Is there a wavelength limit?“ Dyes and Pigments 177 (Juni 2020): 108313. http://dx.doi.org/10.1016/j.dyepig.2020.108313.
Collot, Mayeul, Rémy Kreder, Anatoliy L. Tatarets, Leonid D. Patsenker, Yves Mely und Andrey S. Klymchenko. „Bright fluorogenic squaraines with tuned cell entry for selective imaging of plasma membrane vs. endoplasmic reticulum“. Chemical Communications 51, Nr. 96 (2015): 17136–39. http://dx.doi.org/10.1039/c5cc06094j.
Ta, Daniel D., und Sergei V. Dzyuba. „Squaraine-Based Optical Sensors: Designer Toolbox for Exploring Ionic and Molecular Recognitions“. Chemosensors 9, Nr. 11 (25.10.2021): 302. http://dx.doi.org/10.3390/chemosensors9110302.
Ryazantsev, Dmitry Y., Maksim V. Kvach, Dmitry A. Tsybulsky, Igor A. Prokhorenko, Irina A. Stepanova, Yury V. Martynenko, Sergey V. Gontarev, Vadim V. Shmanai, Sergey K. Zavriev und Vladimir A. Korshun. „Design of molecular beacons: 3′ couple quenchers improve fluorogenic properties of a probe in real-time PCR assay“. Analyst 139, Nr. 11 (2014): 2867–72. http://dx.doi.org/10.1039/c4an00081a.
Muñoz Resta, Ignacio, und Francisco Galindo. „Phenol-based styrylpyrylium dyes for trace water detection via chromogenic and fluorogenic responses“. Dyes and Pigments 197 (Januar 2022): 109908. http://dx.doi.org/10.1016/j.dyepig.2021.109908.