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II-B08 is a small molecule inhibitor targeting several protein tyrosine phosphatases (PTPs), including SHP2, SHP1, PTP1B, FAP1, CD45, LMWPTP, and Lyp. It acts as a reversible and non-competitive inhibitor, showing 2.6- to 5.7-fold selectivity for SHP2 over related phosphatases. II-B08 is primarily used in phosphorylation and dephosphorylation research, and is effective in blocking hyperproliferative activity of hematopoietic progenitor cells and c-kit-dependent myeloid proliferation. This agent is investigated for potential utility in myeloproliferative disease models associated with c-kit or SHP2 mutations, and is used in combination studies with PI-3K inhibitors to prolong survival in preclinical models[1][9].
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