Development of Selective Pyrido[2,3-d]pyrimidin-7(8H)-one-Based Mammalian STE20-Like (MST3/4) Kinase Inhibitors

Approved

Classifications

MinEdu publication type
A1 Journal article (peer-reviewed)
Definition
Article
Target group
Scientific
Peer reviewed
Peer-reviewed
Article type
Journal article
Host publication type
Journal

Authors of the publication

Number of authors
18
Authors
Rak, Marcel; Menge, Amelie; Tesch, Roberta; Berger, Lena M; Balourdas, Dimitrios-Ilias; Shevchenko, Ekaterina; Kramer, Andreas; Elson, Lewis; Berger, Benedict-Tilman; Abdi, Ismahan; Wahl, Laurenz M; Poso, Antti; Kaiser, Astrid; Hanke, Thomas; Kronenberger, Thales; Joerger, Andreas C; Muller, Susanne; Knapp, Stefan

Publication channel information

Title of journal/series
Journal of medicinal chemistry
ISSN (print)
0022-2623
ISSN (electronic)
1520-4804
ISSN (linking)
0022-2623
Publication forum ID
61000
Publication forum level
3
Internationality
Yes

Detailed publication information

Publication year
2024
Reporting year
2024
Journal/series volume number
67
Journal/series issue number
5
Page numbers
3813-3842
DOI
10.1021/acs.jmedchem.3c02217
Language of publication
English

Co-publication information

International co-publication
Yes
Co-publication with a company
No

Availability

Classification and additional information

MinEdu field of science classification
317 Pharmacy

Funding information

Funding information in the publication
The authors are grateful to the Structural Genomics Consortium (SGC), a registered charity (no. 1097737) that received funds from Bayer AG, Boehringer Ingelheim, Bristol Myers Squibb, Genentech, Genome Canada through Ontario Genomics Institute, Janssen, Merck KGaA, Pfizer, and Takeda. This project received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under Grant 875510. The JU receives support from the European Union's Horizon 2020 research and innovation program, EFPIA, Ontario Institute for Cancer Research, Royal Institution for the Advancement of Learning McGill University, Kungliga Tekniska Hoegskolan, and Diamond Light Source Limited. M R. is grateful for the support by the Dr. Hilmer-Stiftung. A.M. is supported by the German Research Foundation (DFG) Grant 259130777 (SFB1177), and B.-T. B. and S.K. are grateful for support by the SFB1399 (Grant 413326622). R.T. was supported by the German Research Foundation (DFG) Grant 397659447. A.C.J. is supported by the German Research Foundation (DFG) Grant JO 1473/1-3. T.H. and S.K. are grateful for support by the ENABLE project "Unraveling mechanisms driving cellular homeostasis, inflammation and infection to enable new approaches in translational medicine". The CQ1 microscope was funded by FUGG (INST 161/920-1 FUGG). We want to thank Julia Frischkorn for her passionate cell culture work. Data collection at the Swiss Light Source (SLS) was supported by funding from the European Union's Horizon 2020 research and innovation program Grant 730872, project CALIPSOplus. We also thank the staff at SLS beamline X06SA for assistance during data collection. T.K., A.P. and E.S. would like to thank TuCAD2, which is funded by the Federal Ministry of Education and Research (BMBF) and the Baden-Wurttemberg Ministry of Science as part of the Excellence Strategy of the German Federal and State Governments EXC 2180-390900677. T.K. is supported by the Fortune initiative (no. 2613-0-0) and by the iFIT, which are both initiatives from the Excellence Strategy of the German Federal and State Governments. We thank CSC-Finland for the generous computational resources provided.

Source database ID

WoS ID
WOS:001178730700001
Scopus ID
2-s2.0-85186372970