2023
DOI: 10.1039/d3tc03664b
|View full text |Cite
|
Sign up to set email alerts
|

Recent progress of organic fluorescent molecules for bioimaging applications: cancer-relevant biomarkers

Chun Zhang,
Yi-Tao Sun,
Suya Gan
et al.

Abstract: The work reports the progress of small-fluorescent molecules for bioimaging applications to cancer-relevant biomarkers H+, NO, H2S and reactive oxygen species (H2O2, HClO, O2˙−, 1O2 and ˙OH) over the past six years.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
0
0

Year Published

2024
2024
2025
2025

Publication Types

Select...
4

Relationship

1
3

Authors

Journals

citations
Cited by 4 publications
(1 citation statement)
references
References 112 publications
0
0
0
Order By: Relevance
“…Our group had been focusing on the development of PTP modulators for decades, and developed several fluorescent SHP1 inhibitors as tools to investigate the SHP1 biological function in the complex and dynamic intracellular environment. Thus, to enrich the diversity of SHP1 fluorescent inhibitor skeletons, all the synthesized isatin compounds were further evaluated against SHP1 PTP by using a broad-spectrum phosphatase inhibitor, NSC87877, as a positive control for SHP1 PTP . Among compounds 3a–3f , compounds with an electron-donor group (−NH 2 , −OMe) and an alkyl group (-methyl, -ethyl, -propyl) on the phenyl ring showed weaker inhibitory activities than the corresponding compound 3a .…”
Section: Resultsmentioning
confidence: 99%
“…Our group had been focusing on the development of PTP modulators for decades, and developed several fluorescent SHP1 inhibitors as tools to investigate the SHP1 biological function in the complex and dynamic intracellular environment. Thus, to enrich the diversity of SHP1 fluorescent inhibitor skeletons, all the synthesized isatin compounds were further evaluated against SHP1 PTP by using a broad-spectrum phosphatase inhibitor, NSC87877, as a positive control for SHP1 PTP . Among compounds 3a–3f , compounds with an electron-donor group (−NH 2 , −OMe) and an alkyl group (-methyl, -ethyl, -propyl) on the phenyl ring showed weaker inhibitory activities than the corresponding compound 3a .…”
Section: Resultsmentioning
confidence: 99%