" /> SHP2 Inhibitor BBP-398 - CISMeF





Preferred Label : SHP2 Inhibitor BBP-398;

NCIt definition : An orally bioavailable inhibitor of protein tyrosine phosphatase (PTP) non-receptor type 11 (SHP2; Src homology region 2 domain phosphatase; PTPN11), with potential antineoplastic activity. Upon oral administration, SHP2 inhibitor BBP-398 targets, allosterically binds to and inhibits the activity of SHP2. This prevents SHP2-mediated signaling, inhibits MAPK signaling and prevents growth of SHP2-expressing tumor cells. SHP2, an oncoprotein overexpressed in a variety of cancer cell types, regulates cell survival, differentiation and proliferation through activation of the Ras-Raf-MEK-ERK signaling pathway. The Ras-MAPK pathway is often hyperactivated in cancer cells due to specific mutations and rearrangements which are dependent on SHP2 for their oncogenic signaling. SHP2 also regulates programmed cell death 1 (PD-1)-mediated signal transduction and is involved in immune checkpoint modulation.;

Molecule name : BBP-398; IACS-15509; IACS 15509; BBP 398; BMS-986466; BMS 986466;

NCI Metathesaurus CUI : CL1643294;

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10/05/2024


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