Design, synthesis, and biological evaluation of novel derivatives of dithiodiglycolic acid prepared via oxidative coupling of thiols.
2019
Преузимање 🢃
Аутори:
Bakulina, OlgaBannykh, Anton
Jovanović, Mirna
Domračeva, Ilona
Podolski-Renić, Ana
Žalubovskis, Raivis
Pešić, Milica
Dar'in, Dmitry
Krasavin, Mikhail
Тип документа:
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт:
Human thioredoxin reductase 1 (TrxR1) is a selenocysteine-containing enzyme which plays a crucial role in regulating numerous redox signalling pathways within the cell. While its functioning is important in all cells, levels of TrxR1 expression are higher in cancer cells, possibly as an adaptation to much higher levels of reactive oxygen species and the need for more extensive DNA synthesis. This makes TrxR1 an attractive target for cancer therapy development. Inspired by the structure of disulphide compounds which have advanced through various stages of clinical development, we designed a series of dithiodiglycolic acid derivatives. These were prepared from respective thiol synthons using an iodine- or benzotriazolyl chloride-promoted oxidative disulphide bond formation. Inhibition of TrxR present in cell lysates from human neuroblastoma cells (SH-SY5Y) and rat liver cells indicated several compounds with a potential for TrxR inhibition. Some of these compounds were also tested for growth inhibition against two human cancer cell lines and normal human keratinocytes.
Кључне речи:
TrxR; Anticancer activity; Disulphide inhibitors; Dithiodiglycolic acidИзвор:
Journal of Enzyme Inhibition and Medicinal Chemistry, 2019, 34, 1, 665-671Финансирање / пројекти:
- Идентификација молекуларних маркера за предикцију прогресије тумора, одговора на терапију и исхода болести (RS-MESTD-Integrated and Interdisciplinary Research (IIR or III)-41031)
- Russian Foundation for BasicResearch [project grant 18–515-76001
- ERA.Net RUS plus joint programmegrant RUS_ST2017-309 and State Education Development Agencyof Republic of Latvia (“THIOREDIN”)
- COST Action CM1407
DOI: 10.1080/14756366.2019.1575372
PubMed: 30746961
WoS: 000458393200001
Scopus: 2-s2.0-85061406486
URI
https://www.tandfonline.com/doi/full/10.1080/14756366.2019.1575372http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=PMC6374954
https://radar.ibiss.bg.ac.rs/handle/123456789/3266