Arylidene-Imidazolones with Three Electron-Donating Substituents as Fluorogenic Dyes for Lipid Droplets of Living Cells

Objective: A pair of fluorogenic dyes with three electron-donating groups, based on arylideneimidazolones, is presented. Methods: The formation of imines of the corresponding aldehydes with the subsequent [3 + 2] cycloaddition was used for the synthesis of arylidene-imidazolones. The optical properties of the new compounds were studied. The fluorescence microscopy was used for imaging lipid droplets of the living cells, labeled by the dyes. Results and Discussion: We discovered that a pair of the proposed substances is characterized by a significant bathochromic shift of the absorption and emission maxima, as well as by a noticeable variation of the position of the emission maximum depending on the properties of the environment. We demonstrated that (Z)-5-(3,5-bis(dimethylamino)-4-(ethylamino)benzylidene)-2,3-dimethyl-3,5-dihydro-4H-imidazol-4-one can stain lipid droplets in HeLa Kyoto and Huh 7.5 cell lines. Conclusions: We designed a new selective fluorogenic dye based on arylidene-imidazolones and showed that it can be applicable for lipid droplets labeling in living cells.

Authors

Institutions

Publication Details

Journal
Russian Journal of Bioorganic Chemistry
Published
2025-02-01
DOI
https://doi.org/10.1134/s1068162025010133
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Arylidene-Imidazolones with Three Electron-Donating Substituents as Fluorogenic Dyes for Lipid Droplets of Living Cells

Михаил С. Баранов, Aidar R. Gilvanov, Alexander Yu. Smirnov, D. I. Rudik et al.
Russian Journal of Bioorganic Chemistry
Fluorine in Organic Chemistry
article

Arylidene-Imidazolones with Three Electron-Donating Substituents as Fluorogenic Dyes for Lipid Droplets of Living Cells

Михаил С. Баранов, Aidar R. Gilvanov, Alexander Yu. Smirnov, D. I. Rudik, S. A. Krasnova, Yu. А. Bogdanova
article en

Abstract

Objective: A pair of fluorogenic dyes with three electron-donating groups, based on arylideneimidazolones, is presented. Methods: The formation of imines of the corresponding aldehydes with the subsequent [3 + 2] cycloaddition was used for the synthesis of arylidene-imidazolones. The optical properties of the new compounds were studied. The fluorescence microscopy was used for imaging lipid droplets of the living cells, labeled by the dyes. Results and Discussion: We discovered that a pair of the proposed substances is characterized by a significant bathochromic shift of the absorption and emission maxima, as well as by a noticeable variation of the position of the emission maximum depending on the properties of the environment. We demonstrated that (Z)-5-(3,5-bis(dimethylamino)-4-(ethylamino)benzylidene)-2,3-dimethyl-3,5-dihydro-4H-imidazol-4-one can stain lipid droplets in HeLa Kyoto and Huh 7.5 cell lines. Conclusions: We designed a new selective fluorogenic dye based on arylidene-imidazolones and showed that it can be applicable for lipid droplets labeling in living cells.

Russian Journal of Bioorganic ChemistryVol. 51(1)
Pirogov Russian National Research Medical University (RU), Institute of Bioorganic Chemistry (RU)
Zero hunger
Openalex Percentile: Top 98%
Fluorine in Organic Chemistry
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Arylidene-Imidazolones with Three Electron-Donating Substituents as Fluorogenic Dyes for Lipid Droplets of Living Cells — Михаил С. Баранов, Aidar R. Gilvanov, et al. · Russian Journal of Bioorganic Chemistry (2025) | TGRS Research Map | TGRS