Combination of quinoxaline with pentamethinium system: Mitochondrial staining and targeting
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22330%2F23%3A43927336" target="_blank" >RIV/60461373:22330/23:43927336 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11110/23:10470086 RIV/60461373:22340/23:43927336 RIV/00064165:_____/23:10470086
Result on the web
<a href="https://www.sciencedirect.com/science/article/pii/S0045206823004777" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0045206823004777</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.bioorg.2023.106816" target="_blank" >10.1016/j.bioorg.2023.106816</a>
Alternative languages
Result language
angličtina
Original language name
Combination of quinoxaline with pentamethinium system: Mitochondrial staining and targeting
Original language description
Pentamethinium indolium salts are promising fluorescence probes and anticancer agents with high mitochondrial selectivity. We synthesized two indolium pentamethinium salts: a cyclic form with quinoxaline directly incorporated in the pentamethinium chain (cPMS) and an open form with quinoxaline substitution in the γ-position (oPMS). To better understand their properties, we studied their interaction with mitochondrial phospholipids (cardiolipin and phosphatidylcholine) by spectroscopic methods (UV–Vis, fluorescence, and NMR spectroscopy). Both compounds displayed significant affinity for cardiolipin and phosphatidylcholine, which was associated with a strong change in their UV–Vis spectra. Nevertheless, we surprisingly observed that fluorescence properties of cPMS changed in complex with both cardiolipin and phosphatidylcholine, whereas those of oPMS only changed in complex with cardiolipin. Both salts, especially cPMS, display high usability in mitochondrial imaging and are cytotoxic for cancer cells. The above clearly indicates that conjugates of pentamethinium and quinoxaline group, especially cPMS, represent promising structural motifs for designing mitochondrial-specific agents.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10401 - Organic chemistry
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2023
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Bioorganic Chemistry
ISSN
0045-2068
e-ISSN
1090-2120
Volume of the periodical
141
Issue of the periodical within the volume
December 2023
Country of publishing house
US - UNITED STATES
Number of pages
12
Pages from-to
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UT code for WoS article
001081516100001
EID of the result in the Scopus database
2-s2.0-85171444339