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This compound is a synthetic, nonpeptide small molecule designed as a ligand for the Src homology 2 (SH2) domain of the Src family tyrosine kinases. It mimics phosphotyrosine-containing sequences and binds to the SH2 domain, thereby inhibiting protein-protein interactions mediated by this domain. The SH2 domain is critical in intracellular signaling pathways, particularly those involving tyrosine kinases such as Src, which are implicated in cancer and other diseases. This molecule was developed for proof-of-concept studies to explore inhibition of SH2-phosphoprotein interactions as a therapeutic strategy[5][6][8].
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