Development of a Direct-to-Biology Platform to Discover Potent MNK Inhibitors

values as low as 23 nM in LN229 cells. This work establishes a D2B approach as an effective strategy for efficient kinase inhibitor optimization.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2026-05-13
DOI
https://doi.org/10.1021/acs.jmedchem.6c00368
Primary Topic
Melanoma and MAPK Pathways
Type
article
Field-Weighted Citation Impact
0.00

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article

Development of a Direct-to-Biology Platform to Discover Potent MNK Inhibitors

Leonidas C. Platanias, Yingyu Mao, Purav P. Vagadia, Frank Eckerdt et al.
Journal of Medicinal Chemistry
Melanoma and MAPK Pathways
article

Development of a Direct-to-Biology Platform to Discover Potent MNK Inhibitors

Leonidas C. Platanias, Yingyu Mao, Purav P. Vagadia, Frank Eckerdt, Joshua L. Zhu, Gary E. Schiltz
article en

Abstract

values as low as 23 nM in LN229 cells. This work establishes a D2B approach as an effective strategy for efficient kinase inhibitor optimization.

Journal of Medicinal Chemistry
Jesse Brown VA Medical Center (US), High Throughput Biology (United States) (US), Robert H. Lurie Comprehensive Cancer Center of Northwestern University
State of Illinois, International Institute for Nanotechnology, Northwestern University, NIH Office of the Director, National Cancer Institute, National Institute of Neurological Disorders and Stroke, Division of Electrical, Communications and Cyber Systems
Openalex Percentile: Top 8%
Melanoma and MAPK Pathways
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