TBAP-001 (Synthesis 13), extracted from patent WO2015075483A1, is a pan-RAF kinase inhibitor, with an IC 50 of 62 nM in BRAF V600E kinase assay In Vitro BAP-001 (Synthesis 13) exhibits IC 50 values of 178 nM (A375), 62 nM (WM266.4), 72 nM (UACC62), 93 nM (LOX INVI), 590 nM (HT 29), 43 nM (COLO225), 690 nM (RKO), 490 nM (Mawi), 390 nM (WiDr), 480 nM (Colo741), 480 nM (SW620), 600 nM (HCT116), 390 nM (SKMEL2), 710 nM (D04), 390 nM (WM1361), 1150 nM (PDAC R172H (p53 mut)), 290 nM (MiaPaCa) and 490nM (RPMI8226) in different cancer cell lines. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid IC50& Target:IC50: 62 nM (BRAF V600E kinase assay), 18 nM (Cell-Based Phosho-ERK Assay)
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TBAP-001
CAS number:1777832-90-2 molecular formula:C27H23F2N7O3
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| Chinese alias | - | ||
| English alias | - | ||
| CAS number | 1777832-90-2 | molecular formula | C27H23F2N7O3 |
| molecular weight | 531.51 g/mol | Exact mass | ≥99% |
| PSA | 123.000 Ų | logp | 4.300 |
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