Synthesis of 4-styrylpyrazoles and Evaluation of their Inhibitory Effects on Cyclin-dependent Kinases
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu časopisecké články
Grantová podpora
IGA_PRF_2021_024
Internal Grant Agency of Palacký University
21-06553S
Czech Science Foundation
PubMed
34365958
DOI
10.2174/1573406417666210806095710
PII: MC-EPUB-117119
Knihovny.cz E-zdroje
- Klíčová slova
- CAN508, CDK inhibitors, K562, Suzuki-Miyaura cross-coupling reaction, Vilsmeier-Haack reaction, styrylpyrazoles,
- MeSH
- buněčný cyklus MeSH
- cyklin-dependentní kinasy metabolismus farmakologie MeSH
- fosforylace MeSH
- inhibitory proteinkinas chemie MeSH
- lidé MeSH
- nádory * farmakoterapie MeSH
- protinádorové látky * chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- cyklin-dependentní kinasy MeSH
- inhibitory proteinkinas MeSH
- protinádorové látky * MeSH
BACKGROUND: Cycle-regulating and transcriptional cyclin-dependent kinases (CDKs) are attractive targets in cancer drug development. Several CDK inhibitors have already been obtained or are close to regulatory approval for clinical applications. OBJECTIVE: Phenylazopyrazole CAN508 has been described as the first selective CDK9 inhibitor with an IC50 of 350 nM. Since the azo-moiety is not a suitable functionality for drugs due to pharmacological reasons, the preparation of carbo-analogues of CAN508 with similar biological activities is desirable. The present work is focused on the synthesis of carbo-analogues similar to CAN508 and their CDK inhibition activity. METHODS: Herein, the synthesis of 21 novel carbo analogues of CAN508 and their intermediates is reported. Subsequently, target compounds 8a - 8u were evaluated for protein kinase inhibition (CDK2/cyclin E, CDK4/cyclin D, CDK9/cyclin T) and antiproliferative activities in cell lines (K562, MCF-7, MV4-11). Moreover, the binding mode of derivative 8s in the active site of CDK9 was modelled. RESULTS: Compounds 8a - 8u were obtained from key intermediate 7, which was prepared by linear synthesis involving Vilsmeier-Haack, Knoevenagel, Hunsdiecker, and Suzuki-Miyaura reactions. Styrylpyrazoles 8t and 8u were the most potent CDK9 inhibitors with IC50 values of approximately 1 μM. Molecular modelling suggested binding in the active site of CDK9. The flow cytometric analysis of MV4-11 cells treated with the most active styrylpyrazoles showed a significant G1-arrest. CONCLUSION: The prepared styrylpyrazoles showed inhibition activity towards CDKs and can provide a novel chemotype of kinase inhibitors.
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