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Near infrared fluorescent probes for detecting and imaging active small molecules
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“Most small-molecule organic fluorophores are constructed around key structural scaffolds such as cyanine, boron dipyrromethene (BODIPY), benzobisthiadiazole (BBTD), xanthene, cyano-based derivatives and small-molecule metal complexes, which serve as their fundamental emissive cores71,72.”
From Organic small-molecule NIR-II fluorophores for tumor phototheranostics (2026) · cites this paper as [72]
Citations
Cites
Modulation of oxidative stress as an anticancer strategy
Gorrini, C., Harris, I. S., & Mak, T. W. (2013) · Nature Reviews Drug Discovery · doi:10.1038/nrd4002 · Cited by 3,579
In vivo near-infrared fluorescence imaging
Frangioni, J. V. (2003) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2003.08.007 · Cited by 2,701
Luminescent Chemodosimeters for Bioimaging
Yang, Y., Zhao, Q., Feng, W., & Li, F. (2012) · Chemical Reviews · doi:10.1021/cr2004103 · Cited by 2,244
Multiphoton Absorbing Materials: Molecular Designs, Characterizations, and Applications
He, G. S., Tan, L., Zheng, Q., & Prasad, P. N. (2008) · Chemical Reviews · doi:10.1021/cr050054x · Cited by 2,200
Yuan, L., Lin, W., Zheng, K., He, L., & Huang, W. (2012) · Chemical Society Reviews · doi:10.1039/c2cs35313j · Cited by 1,825
Recent progress in the development of near-infrared fluorescent probes for bioimaging applications
Guo, Z., Park, S., Yoon, J., & Shin, I. (2013) · Chemical Society Reviews · doi:10.1039/c3cs60271k · Cited by 1,812
Design Strategies for Water-Soluble Small Molecular Chromogenic and Fluorogenic Probes
Li, X., Gao, X., Shi, W. S., & Ma, H. (2013) · Chemical Reviews · doi:10.1021/cr300508p · Cited by 1,745
A new trend in rhodamine-based chemosensors: application of spirolactam ring-opening to sensing ions
Kim, H. N., Lee, M. H., Kim, H. J., Kim, J. S., & Yoon, J. (2008) · Chemical Society Reviews · doi:10.1039/b802497a · Cited by 1,652
Cyanines during the 1990s: A Review
Mishra, A., Behera, R. K., Behera, P. K., Mishra, B. K., & Behera, G. B. (2000) · Chemical Reviews · doi:10.1021/cr990402t · Cited by 1,565
Synthesis and applications of Rhodamine derivatives as fluorescent probes
Beija, M., Afonso, C. A. M., & Martinho, J. M. G. (2009) · Chemical Society Reviews · doi:10.1039/b901612k · Cited by 1,498
Research works printed but not linked: 8
- Zhang, 2021, Cell Rep. Phys. Sci., 2
- Liu, 2022, Coord. Chem. Rev., 468
- Cheng, 2022, Adv. Mater., e2207546
- Fan, 2023, Coord. Chem. Rev., 480
- An, 2022, Talanta, 253
- Li, 2022, Angew. Chem. Int. Ed. Engl., e202217326
- Kim, 2021, Nanomicro Lett., 13, 168
- Zhang, 2020, J. Hazard. Mater., 396
Cited by
Sorted by citations
Items 201–247 of 247
Zou, J., Liu, Y., Sun, Y., Liu, H., Chen, Z., Liu, G., & Pu, S. (2026) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2026.128633 · Cited by 1
Liang, X., Wang, C., Liang, T., Tian, M., Wu, C., Li, Y., Zhong, K., Shen, T., & Tang, L. (2026) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2026.119116 · Cited by 1
Mandloi, U., Giri, N., Kumar, S., & Modi, G. P. (2026) · RSC Medicinal Chemistry · doi:10.1039/d5md00713e · Cited by 1
Peng, W., Zhang, J., Wen, Z., Liu, M., Ye, B., Zhang, X., Wang, F., Liu, H., & Yu, F. (2026) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2026.139615 · Cited by 1
Lee, S. B., Choi, M., Son, Y. H., Kim, M., Park, H. K., Kim, S. H., Juraev, O. O. U., Jung, H., Bae, H. E., Jeong, J., et al. (2026) · Small · doi:10.1002/smll.202512617 · Cited by 1
Abad-Montero, D., Bosch, M., Garcés‐Castellanos, R., Schottenhamel, M. Q., Pedraza‐Arévalo, S., Ibáñez‐Costa, A., Castano, J. P., Garcia‐Becerra, T., Rebollo, E., Alberto, M. E., et al. (2026) · Angewandte Chemie International Edition · doi:10.1002/anie.9647759 · Cited by 1
Yang, Q., Yao, Y., Zeng, F., Ma, J., Wu, L., Xing, S., Yang, H., Li, Y., Du, J., & Li, Y. (2023) · SSRN Electronic Journal · doi:10.2139/ssrn.4617495
Zhu, Y., Rong, X., Zheng, M., Liu, C., Wang, Y., Wen, H., Sheng, W., & Zhu, B. (2025) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2025.108704
Xia, H., Wang, X., Huang, W., Jiang, X., Han, X., & Wang, C. (2025) · Frontiers in Chemistry · doi:10.3389/fchem.2025.1666238
Rosales‐Hurtado, M., Liénart, L., Lunova, V., Banères, J., Cuminal, Y., Clément, S., Fehrentz, J., van der Lee, A., Cavelier, F., & Rémond, E. (2025) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.5c00342
Sun, C., Yang, S., Yan, X., Liao, H., Xia, T., Xun, Y., Chen, X., Yan, S., Liu, L., & Bai, J. (2025) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.5c14666
A novel near-infrared COX-2 targeting probe for tumor and metastatic lymph node monitoring
Yu, A., Li, Y., Wang, Y., He, J., Zhou, Y., Cai, H., Wang, Y., Dai, B., & Shen, Y. (2026) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2026.109645
Arruda, C., Müer, P. H., Pietezak, D. F., Xavier, F. R., Oliboni, R. S., Santos, A. A. D., & Gariani, R. A. (2026) · Dyes and Pigments · doi:10.1016/j.dyepig.2026.113765
Bai, S., Feng, B., Dong, Q., & Liu, M. (2026) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2026.109922
Lv, S., Yang, L., Wu, C., Liu, Y., He, Y., Cao, Y., Li, P., Wang, Z., & Zhu, H. (2026) · Analytica Chimica Acta · doi:10.1016/j.aca.2026.345613
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Advances in near-infrared fluorescent probes for the tumor microenvironment
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Lian, Q., Weng, Q., He, M., Li, L., Huang, Z., Li, D., & Lu, B. (2026) · Talanta · doi:10.1016/j.talanta.2026.130046
Peptide‐based responsive molecular fluorescent probes for precision oncology
Wang, X., Liu, W., Zhang, J., Wang, W., Jin, Z., Tang, Y., & Li, Q. (2026) · Responsive materials · doi:10.1002/rpm2.70064
Benzothiazole–based molecular rotor as near-infrared (NIR) fluorescent probes for viscosity sensing
Junjai, W., Sangtawesin, S., Aryamueang, S., Trakarnthai, N., Kusoltech, C., Saengboonmee, C., & Kamkaew, A. (2026) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2026.110152
Abad-Montero, D., Bosch, M., Garcés‐Castellanos, R., Schottenhamel, M. Q., Pedraza‐Arévalo, S., Ibáñez‐Costa, A., Castano, J. P., Garcia‐Becerra, T., Rebollo, E., Alberto, M. E., et al. (2026) · Angewandte Chemie · doi:10.1002/ange.9647759
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Wan, F., He, J., Liu, Y., Zhu, J., & Li, Z. L. (2026) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2026.218248
Li, Q., Cui, D.-X., Leng, Y., Shou-jun, L. A. I., Deng, T., Niu, T., Yang, S., & Dong, H. (2026) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2026.146955
Chen, Z., Shi, Y., Jiang, L., Yin, Y., Yang, L., Huang, X., Jiang, L., guo, W., Liu, X., Fu, R., et al. (2026) · Journal of the American Chemical Society · doi:10.1021/jacs.6c06089
Wang, F., Jiang, X., Yu, K., Wang, Y., Li, J., Ling, Y., Feng, Z., Hu, L., & Wang, H. (2026) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2026.147015
ZHANG, C., & Wang, J. (2026) · Photochemical & Photobiological Sciences · doi:10.1007/s43630-026-00951-8
Liu, J., Zhai, P., Pan, R., Li, X., Tang, S., & Shu, W. (2026) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2026.128445
Nie, C., Yan, S., Xing, G., Ji, K., Yang, X., Tang, J., Chen, J., Zhao, Y., Hu, J., & Liu, J. (2026) · Journal of Luminescence · doi:10.1016/j.jlumin.2026.122086
Chen, K., Yuwen, Z., Lu, C., Zhang, Z., Zhang, D., Yang, Y., & Liu, H. (2026) · Analytical Methods · doi:10.1039/d6ay01510g
Spiro-helicenoid Carbofluoresceins: CPL-Active Emitters for Bioimaging
Erviti-Marticorena, L., Simón‐Fuente, S., Míguez‐Lago, S., Paredes, J. M., Ribagorda, M., Girón, M. D., Millán, A., Cuerva, J. M., & Miguel, D. (2026) · Organic Letters · doi:10.1021/acs.orglett.6c02744
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Ma, W., Gu, Q., Lv, Q., Duan, Q.-C., Cao, Z., Sun, K., & Yu, B. (2026) · Chemistry - A European Journal · doi:10.1002/chem.71600
Pang, Y., & Zhou, L. (2026) · The Analyst · doi:10.1039/d6an00706f
Zhao, H., Jiang, M., Song, A., Sun, W. Y., Li, G., Li, J., Yang, X., Zhang, X., Li, S., & Zhao, Q. (2026) · Advanced Functional Materials · doi:10.1002/adfm.77953
β-Galactosidase-responsive AIE fluorescent probe for tumor-targeted imaging and photodynamic therapy
Yang, L., Lu, X., Chen, N., Zhu, H., Liu, T., & Li, Z. (2026) · Chinese Chemical Letters · doi:10.1016/j.cclet.2026.113342
Wang, B., Sun, J., Ding, C., Zhang, Y., Zhu, Q., Zhang, T., & Wang, F. (2026) · Journal of Material Science and Technology · doi:10.1016/j.jmst.2026.08.041
Self-citationHu, L., Li, T., Zeng, S., Ouyang, J., Huang, S., Sun, D., Yang, Z., Wang, Q., Yao, Z., & Li, C. (2026) · Talanta · doi:10.1016/j.talanta.2026.130568
Gong, Y., Shi, W., Ma, A., Wang, Q., Lou, W., & Zhang, M. (2026) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-026-06782-x
Zeng, Y., Zhou, Z., Yu, J., Jiang, H., Shen, Y., & Liu, X. (2026) · SSRN Electronic Journal · doi:10.2139/ssrn.7499769
Corbin, B., Mason, J., Houglan, P. M., Murphey, A., & Pang, Y. (2026) · Biosensors · doi:10.3390/bios16100533
Hu, X., Song, X., Qiu, Y., & Du, W. (2026) · Biosensors · doi:10.3390/bios16100540
Gong, Y., Shi, W., Ma, A., Wang, Q., & Zhang, M. (2026) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2026.140998
Zuo, X., Li, Y., 阮馨平, Zhao, B., Li, X., Wang, W., & Zhang, Y. (2026) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2026.128871
One-Pot Michael Addition–Elimination Approach to 4-Carboranylcoumarin-Derived Luminescent Systems
Fatykhov, R. F., Lavrinchenko, I. A., Gurina, E. M., Sharapov, A. D., Khalymbadzha, I. А., Вараксин, М. В., Гавико, В. С., Moseev, T. D., & Чупахин, О. Н. (2026) · Organic Letters · doi:10.1021/acs.orglett.6c03900
Structural engineering strategies of near-infrared two-photon probes
Yan, F., Liu, Y., Zhang, Y., Su, D., Wang, C., Ma, S., Wang, L., Miao, Q., Chen, P., Tang, B., et al. (2026) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2026.218682
Metadata
- Authors
- Ding, C., & Ren, T.
- Affiliations
- Hangzhou Normal University (CN)
- Corresponding author
- Ding, Caiping
- Venue
- Coordination Chemistry Reviews
- Publisher
- Elsevier BV
- Published
- 2023-05
- Volume
- 482
- Pages
- 215080
- ISSN
- 0010-8545 (ISSN-L)
- OpenAlex
- W4321442069
- Cited by
- 247
- References
- 131
- Citations by year
- 2026: 63 · 2025: 91 · 2024: 64 · 2023: 29
- FWCI
- 22.81
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Coordination Chemistry Reviews (publishedVersion)
- Funders
- National Natural Science Foundation of China (22004033, 22005081)
- Natural Science Foundation of Zhejiang Province (LY22B050003)
- Topics
- Physical Sciences › Chemistry › Spectroscopy › Molecular Sensors and Ion Detection
- Physical Sciences › Materials Science › Materials Chemistry › Luminescence and Fluorescent Materials
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Sulfur Compounds in Biology
- Keywords
- near-infrared fluorescent probe, fluorophores, BODIPY, cyanine dyes, rhodamine, coumarins, reactive oxygen species, reactive nitrogen species, in vivo imaging, small molecule detection
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