Biochemical Reagent
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BA6530 BI-882370Summary: BI-882370 is a highly potent and selective kinase inhibitor whose binding is located at the DFG-out inactive conformation of the kinase (ATP binding site). - BA6531 AD80Summary: Inhibitor of several kinases.
- BA6532 RAF709Summary: RAF709 is a potent inhibitor.
- BA6533 HG6-64-1Summary: HG6-64-1 is a potent and selective inhibitor.
- BA6534 CFT1946Summary: CFT1946 is an orally active, CRBN-based mutation-selective bifunctional degradation-activating compound (BiDAC) degrader with a DC of 14 nM in A375 cells.
- BA6535 TinlorafenibSummary: Tinlorafenib (PF-07284890) is an orally effective inhibitor.
- BA6536 GNE-9815Summary: GNE-9815 (Compound 7) is a highly selective pan-type inhibitor with good oral bioavailability.
- BA6537 PLX7922Summary: PLX7922 is an inhibitor that binds to BRAFV600E.
- BA6538 TBAP-001Summary: TBAP-001 is a pan-inhibitor of kinases.
- BA6539 LUT014Summary: LUT014 is an inhibitor.