Small-Molecule Intervention At The Dimerization Interface Of Survivin By Novel Rigidized Scaffolds
Autor: | Christoph M. Ernst, Tamer M. Ibrahim, Frank M. Boeckler, Andreas Lange, Susanne Hennig |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Pharmacology INCENP Chemistry In silico Mutant Substituent Pharmaceutical Science Small molecule law.invention 03 medical and health sciences chemistry.chemical_compound 030104 developmental biology 0302 clinical medicine law 030220 oncology & carcinogenesis Drug Discovery Survivin Cancer cell Recombinant DNA Biophysics |
Zdroj: | Drug Design, Development and Therapy. 13:4247-4263 |
ISSN: | 1177-8881 |
Popis: | Introduction Survivin is a nodal protein involved in several cellular pathways. It is a member of the IAP family and an integral component of the chromosomal passenger complex, where it binds to borealin and INCENP through its dimerization interface. By targeting survivin with a small molecule at its dimerization interface, inhibition of the proliferation of cancer cells has been suggested. With Abbott 8, a small-molecule dimerization inhibitor has been recently reported. The structure-activity relationship of this series of inhibitors implied that the middle pyridin-2(1H)-one ring did not tolerate modifications of any kind. Methods Based on the synthetic strategy of Abbott 8 using multicomponent reactions, we synthesized a series of small molecules bearing a novel rigidized core scaffold. This rigidization strategy was accomplished by integrating the pyridin-2(1H)-one and its 6-phenyl substituent into a tricyclic structure, linking position 5 of pyridin-2(1H)-one to the phenyl substituent by rings of different sizes. The new scaffolds were designed based on in silico molecular dynamics of survivin. Results Binding of these rigidized scaffolds to the recombinant L54M mutant of survivin was evaluated, revealing affinities in the low micromolar range. Conclusion This easily accessible, new class of survivin-dimerization modulators is an interesting starting point for further lead optimization. |
Databáze: | OpenAIRE |
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