Towards New Anti‐Inflammatory Agents: Design, Synthesis and Evaluation of Molecules Targeting XIAP‐BIR2
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Wiley
2024
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| author | Marc Farag Nicolas Guedeney Florian Schwalen Aymeric Zadoroznyj Amélie Barczyk Martin Giret Kevin Antraygues Alice Wang Marie Cornu Peggy Suzanne Marc Since Anne Sophie Voisin‐Chiret Laurence Dubrez Natascha Leleu‐Chavain Charline Kieffer Jana Sopkova‐de Oliveira Santos |
| author_facet | Marc Farag Nicolas Guedeney Florian Schwalen Aymeric Zadoroznyj Amélie Barczyk Martin Giret Kevin Antraygues Alice Wang Marie Cornu Peggy Suzanne Marc Since Anne Sophie Voisin‐Chiret Laurence Dubrez Natascha Leleu‐Chavain Charline Kieffer Jana Sopkova‐de Oliveira Santos Marc Farag Nicolas Guedeney Florian Schwalen Aymeric Zadoroznyj Amélie Barczyk Martin Giret Kevin Antraygues Alice Wang Marie Cornu Peggy Suzanne Marc Since Anne Sophie Voisin‐Chiret Laurence Dubrez Natascha Leleu‐Chavain Charline Kieffer Jana Sopkova‐de Oliveira Santos |
| collection | Wiley Open Access |
| contents | Towards New Anti‐Inflammatory Agents: Design, Synthesis and Evaluation of Molecules Targeting XIAP‐BIR2 Marc Farag Nicolas Guedeney Florian Schwalen Aymeric Zadoroznyj Amélie Barczyk Martin Giret Kevin Antraygues Alice Wang Marie Cornu Peggy Suzanne Marc Since Anne Sophie Voisin‐Chiret Laurence Dubrez Natascha Leleu‐Chavain Charline Kieffer Jana Sopkova‐de Oliveira Santos ChemMedChem AbstractThe X‐chromosome‐linked inhibitor of apoptosis protein (XIAP) plays a crucial role in controlling cell survival across multiple regulated cell death pathways and coordinating a range of inflammatory signalling events. The discovery of selective inhibitors for XIAP‐BIR2, able to disrupt the direct physical interaction between XIAP and RIPK2, offer promising therapeutic options for NOD2‐mediated diseases like Crohn's disease, sarcoidosis, and Blau syndrome. The objective of this study was to design, synthesize, and evaluate small synthetic molecules with binding selectivity to XIAP‐BIR2 domain. To achieve this, we applied an interdisciplinary drug design approach and firstly we have synthesized an initial fragment library to achieve a first XIAP inhibition activity. Then using a growing strategy, larger compounds were synthesized and one of them presents a good selectivity for XIAP‐BIR2 versus XIAP‐BIR3 domain, compound 20 c. The ability of compound 20 c to block the NOD1/2 pathway was confirmed in cell models. These data show that we have synthesized molecules capable of blocking NOD1/2 signalling pathways in cellulo, and ultimately leading to new anti‐inflammatory compounds. 10.1002/cmdc.202400567 http://onlinelibrary.wiley.com/termsAndConditions#vor |
| doi_str_mv | 10.1002/cmdc.202400567 |
| format | Artículo Open Access |
| id | wiley_oa_10_1002_cmdc_202400567 |
| institution | Wiley Open Access |
| license_str_mv | http://onlinelibrary.wiley.com/termsAndConditions#vor |
| publishDate | 2024 |
| publisher | Wiley |
| record_format | wiley_oa |
| spellingShingle | Towards New Anti‐Inflammatory Agents: Design, Synthesis and Evaluation of Molecules Targeting XIAP‐BIR2 Marc Farag Nicolas Guedeney Florian Schwalen Aymeric Zadoroznyj Amélie Barczyk Martin Giret Kevin Antraygues Alice Wang Marie Cornu Peggy Suzanne Marc Since Anne Sophie Voisin‐Chiret Laurence Dubrez Natascha Leleu‐Chavain Charline Kieffer Jana Sopkova‐de Oliveira Santos ChemMedChem Towards New Anti‐Inflammatory Agents: Design, Synthesis and Evaluation of Molecules Targeting XIAP‐BIR2 Marc Farag Nicolas Guedeney Florian Schwalen Aymeric Zadoroznyj Amélie Barczyk Martin Giret Kevin Antraygues Alice Wang Marie Cornu Peggy Suzanne Marc Since Anne Sophie Voisin‐Chiret Laurence Dubrez Natascha Leleu‐Chavain Charline Kieffer Jana Sopkova‐de Oliveira Santos ChemMedChem AbstractThe X‐chromosome‐linked inhibitor of apoptosis protein (XIAP) plays a crucial role in controlling cell survival across multiple regulated cell death pathways and coordinating a range of inflammatory signalling events. The discovery of selective inhibitors for XIAP‐BIR2, able to disrupt the direct physical interaction between XIAP and RIPK2, offer promising therapeutic options for NOD2‐mediated diseases like Crohn's disease, sarcoidosis, and Blau syndrome. The objective of this study was to design, synthesize, and evaluate small synthetic molecules with binding selectivity to XIAP‐BIR2 domain. To achieve this, we applied an interdisciplinary drug design approach and firstly we have synthesized an initial fragment library to achieve a first XIAP inhibition activity. Then using a growing strategy, larger compounds were synthesized and one of them presents a good selectivity for XIAP‐BIR2 versus XIAP‐BIR3 domain, compound 20 c. The ability of compound 20 c to block the NOD1/2 pathway was confirmed in cell models. These data show that we have synthesized molecules capable of blocking NOD1/2 signalling pathways in cellulo, and ultimately leading to new anti‐inflammatory compounds. 10.1002/cmdc.202400567 http://onlinelibrary.wiley.com/termsAndConditions#vor |
| title | Towards New Anti‐Inflammatory Agents: Design, Synthesis and Evaluation of Molecules Targeting XIAP‐BIR2 |
| topic | ChemMedChem |
| url | https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cmdc.202400567 |