8B5Y

SHP2 in complex with allosteric imidazopyrazine inhibitor

Summary for 8B5Y

• Entry DOI: 10.2210/pdb8b5y/pdb
• Descriptor: Tyrosine-protein phosphatase non-receptor type 11, (1~{S})-1'-[5-[2-(trifluoromethyl)pyridin-3-yl]sulfanyl-3~{H}-imidazo[4,5-b]pyrazin-2-yl]spiro[1,3-dihydroindene-2,4'-piperidine]-1-amine, FORMIC ACID, ... (4 entities in total)
• Functional Keywords: shp2, allosteric inhibitors, imidazopyrazine, oncology, signaling protein
• Biological source: Homo sapiens (human)
• Total number of polymer chains: 2
• Total formula weight: 122617.64

Authors

Torrente, E.,Petrocchi, A. (deposition date: 2022-09-25, release date: 2023-01-18, Last modification date: 2024-02-07)

Primary citation

Torrente, E.,Fodale, V.,Ciammaichella, A.,Ferrigno, F.,Ontoria, J.M.,Ponzi, S.,Rossetti, I.,Sferrazza, A.,Amaudrut, J.,Missineo, A.,Esposito, S.,Palombo, S.,Nibbio, M.,Cerretani, M.,Bisbocci, M.,Cellucci, A.,di Marco, A.,Alli, C.,Pucci, V.,Toniatti, C.,Petrocchi, A.
Discovery of a Novel Series of Imidazopyrazine Derivatives as Potent SHP2 Allosteric Inhibitors.
Acs Med.Chem.Lett., 14:156-162, 2023

PubMed Abstract: Protein tyrosine phosphatase SHP2 is an oncogenic protein that can regulate different cytokine receptor and receptor tyrosine kinase signaling pathways. We report here the identification of a novel series of SHP2 allosteric inhibitors having an imidazopyrazine 6,5-fused heterocyclic system as the central scaffold that displays good potency in enzymatic and cellular assays. SAR studies led to the identification of compound , a highly potent SHP2 allosteric inhibitor. X-ray studies showed novel stabilizing interactions with respect to known SHP2 inhibitors. Subsequent optimization allowed us to identify analogue , which possesses excellent potency and a promising PK profile in rodents.

PubMed: 36793438
DOI: 10.1021/acsmedchemlett.2c00454

Experimental method

X-RAY DIFFRACTION (1.83 Å)