Triazole-based estradiol dimers prepared via CuAAC from 17 alpha-ethinyl estradiol with five-atom linkers causing G2/M arrest and tubulin inhibition

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F23%3A73619091" target="_blank" >RIV/61989592:15110/23:73619091 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/60461373:22330/23:43927368

Výsledek na webu

<a href="https://www.sciencedirect.com/science/article/pii/S0045206822007416?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0045206822007416?via%3Dihub</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.bioorg.2022.106334" target="_blank" >10.1016/j.bioorg.2022.106334</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Triazole-based estradiol dimers prepared via CuAAC from 17 alpha-ethinyl estradiol with five-atom linkers causing G2/M arrest and tubulin inhibition

Popis výsledku v původním jazyce

Microtubule dynamic is exceptionally sensitive to modulation by small-molecule ligands. Our previous work presented the preparation of microtubule-targeting estradiol dimer (ED) with anticancer activity. In the present study, we explore the effect of selected linkers on the biological activity of the dimer. The linkers were designed as five-atom chains with carbon, nitrogen or oxygen in their centre. In addition, the central nitrogen was modified by a benzyl group with hydroxy or methoxy substituents and one derivative possessed an extended linker length. Thirteen new dimers were subjected to cytotoxicity assay and cell cycle profiling. Dimers con-taining linker with benzyl moiety substituted with one or more methoxy groups and longer branched ones were found inactive, whereas other structures had comparable efficacy as the original ED (e.g. D1 with IC50 = 1.53 mu M). Cell cycle analysis and immunofluorescence proved the interference of dimers with microtubule assembly and mitosis. The proposed in silico model and calculated binding free energy by the MM-PBSA method were closely correlated with in vitro tubulin assembly assay.

Název v anglickém jazyce

Triazole-based estradiol dimers prepared via CuAAC from 17 alpha-ethinyl estradiol with five-atom linkers causing G2/M arrest and tubulin inhibition

Popis výsledku anglicky

Microtubule dynamic is exceptionally sensitive to modulation by small-molecule ligands. Our previous work presented the preparation of microtubule-targeting estradiol dimer (ED) with anticancer activity. In the present study, we explore the effect of selected linkers on the biological activity of the dimer. The linkers were designed as five-atom chains with carbon, nitrogen or oxygen in their centre. In addition, the central nitrogen was modified by a benzyl group with hydroxy or methoxy substituents and one derivative possessed an extended linker length. Thirteen new dimers were subjected to cytotoxicity assay and cell cycle profiling. Dimers con-taining linker with benzyl moiety substituted with one or more methoxy groups and longer branched ones were found inactive, whereas other structures had comparable efficacy as the original ED (e.g. D1 with IC50 = 1.53 mu M). Cell cycle analysis and immunofluorescence proved the interference of dimers with microtubule assembly and mitosis. The proposed in silico model and calculated binding free energy by the MM-PBSA method were closely correlated with in vitro tubulin assembly assay.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10608 - Biochemistry and molecular biology

Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2023

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

BIOORGANIC CHEMISTRY

ISSN

0045-2068

e-ISSN

1090-2120

Svazek periodika

131

Číslo periodika v rámci svazku

02/2023

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

13

Strana od-do

106334

Kód UT WoS článku

000917336000001

EID výsledku v databázi Scopus

2-s2.0-85145278619