New 2,6,9-trisubstituted purine derivatives as Bcr-Abl and Btk inhibitors and as promising agents against leukemia
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
31699386
DOI
10.1016/j.bioorg.2019.103361
PII: S0045-2068(19)31549-4
Knihovny.cz E-zdroje
- Klíčová slova
- Bcr-Abl inhibitors, Btk inhibitors, Docking, Leukemia, Purine derivatives, QSAR,
- MeSH
- bcr-abl fúzní proteiny antagonisté a inhibitory MeSH
- buňky K562 MeSH
- kvantitativní vztahy mezi strukturou a aktivitou MeSH
- leukemie patologie prevence a kontrola MeSH
- lidé MeSH
- proteinkinasa BTK antagonisté a inhibitory MeSH
- protinádorové látky chemie farmakologie MeSH
- puriny chemie farmakologie MeSH
- signální transdukce účinky léků MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- bcr-abl fúzní proteiny MeSH
- BTK protein, human MeSH Prohlížeč
- proteinkinasa BTK MeSH
- protinádorové látky MeSH
- puriny MeSH
Bcr-Abl and Btk kinases are among the targets that have been considered for the treatment of leukemia. Therefore, several strategies have focused on the use of inhibitors as chemotherapeutic tools to treat these types of leukemia, such as imatinib (for Bcr-Abl) or ibrutinib (for Btk). However, the efficacy of these drugs has been reduced due to resistance mechanisms, which have motivated the development of new and more effective compounds. In this study, we designed, synthesized and evaluated 2,6,9-trisubstituted purine derivatives as novel Bcr-Abl and Btk inhibitors. We identified 5c and 5d as potent inhibitors of both kinases (IC50 values of 40 nM and 0.58/0.66 μM for Abl and Btk, respectively). From docking and QSAR analyses, we concluded that fluorination of the arylpiperazine system is detrimental to the activity against two kinases, and we also validated our hypothesis that the substitution on the 6-phenylamino ring is important for the inhibition of both kinases. In addition, our studies indicated that most compounds could suppress the proliferation of leukemia and lymphoma cells (HL60, MV4-11, CEM, K562 and Ramos cells) at low micromolar concentrations in vitro. Finally, we preliminarily demonstrated that 5c inhibited the downstream signaling of both kinases in the respective cell models. Therefore, 5c or 5d possessed potency to be further optimized as anti-leukemia drugs by simultaneously inhibiting the Bcr-Abl and Btk kinases.
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