Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Westhuizen, Leandi van der | - |
dc.contributor.author | Weisner, Jörn | - |
dc.contributor.author | Taher, Abu | - |
dc.contributor.author | Landel, Ina | - |
dc.contributor.author | Quambusch, Lena | - |
dc.contributor.author | Lindemann, Marius | - |
dc.contributor.author | Uhlenbrock, Niklas | - |
dc.contributor.author | Müller, Matthias P. | - |
dc.contributor.author | Green, Ivan R. | - |
dc.contributor.author | Pelly, Stephen C. | - |
dc.contributor.author | Rauh, Daniel | - |
dc.contributor.author | Otterlo, Willem A. L. van | - |
dc.date.accessioned | 2024-03-04T14:59:07Z | - |
dc.date.available | 2024-03-04T14:59:07Z | - |
dc.date.issued | 2022-02-16 | - |
dc.identifier.uri | http://hdl.handle.net/2003/42375 | - |
dc.identifier.uri | http://dx.doi.org/10.17877/DE290R-24212 | - |
dc.description.abstract | Akt is a protein kinase that has been implicated in the progression of cancerous tumours. A number of covalent allosteric Akt inhibitors are known, and based on these scaffolds, a small library of novel potential covalent allosteric imidazopyridine-based inhibitors was designed. The envisaged compounds were synthesised, with click chemistry enabling a modular approach to a number of the target compounds. The binding modes, potencies and antiproliferative activities of these synthesised compounds were explored, thereby furthering the structure activity relationship knowledge of this class of Akt inhibitors. Three novel covalent inhibitors were identified, exhibiting moderate activity against Akt1 and various cancer cell lines, potentially paving the way for future covalent allosteric inhibitors with improved properties. | en |
dc.language.iso | en | de |
dc.relation.ispartofseries | ChemMedChem;17(10) | - |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | de |
dc.subject | Akt kinase | en |
dc.subject | covalent allosteric inhibitors | en |
dc.subject | imidazopyridines | en |
dc.subject | click chemistry | en |
dc.subject | fragments | en |
dc.subject.ddc | 570 | - |
dc.subject.ddc | 540 | - |
dc.title | Covalent allosteric inhibitors of Akt generated using a click fragment approach | en |
dc.type | Text | de |
dc.type.publicationtype | ResearchArticle | de |
dc.subject.rswk | Protein-Serin-Threonin-Kinasen | de |
dc.subject.rswk | Allosterische Kontrolle | de |
dc.subject.rswk | Imidazopyridine | de |
dc.subject.rswk | Click-Chemie | de |
dc.subject.rswk | Inhibitor | de |
dcterms.accessRights | open access | - |
eldorado.secondarypublication | true | de |
eldorado.secondarypublication.primaryidentifier | https://doi.org/10.1002/cmdc.202100776 | de |
eldorado.secondarypublication.primarycitation | L. van der Westhuizen, J. Weisner, A. Taher, I. Landel, L. Quambusch, M. Lindemann, N. Uhlenbrock, M. P. Müller, I. R. Green, S. C. Pelly, D. Rauh, W. A. L. van Otterlo, ChemMedChem 2022, 17, e202100776. | de |
Appears in Collections: | Medizinische Chemie und Chemische Biologie |
Files in This Item:
File | Description | Size | Format | |
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ChemMedChem - 2022 - Westhuizen - Covalent Allosteric Inhibitors of Akt Generated Using a Click Fragment Approach.pdf | DNB | 4.35 MB | Adobe PDF | View/Open |
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