PROTAC BRAF-V600E degrader-1 is a potent PROTAC BRAF-V600E degrader with K d value of 2.4 nM and 2 nM for BRAF and BRAF-V600E, respectively. PROTAC BRAF-V600E degrader-1 degrades BRAF-V600E via the ubiquitin-proteasome system (UPS). PROTAC BRAF-V600E degrader-1 can inhibit melanoma cell growth In Vitro PROTAC BRAF-V600E degrader-1 (compound 23) (1 nM-10 μM; 72 h) inhibits the cell viability of A375 and HT-29. PROTAC BRAF-V600E degrader-1 (1-1000 nM; 16 h or 0-24 h) inhibits p-ERK and BRAF-V600E protein in A375 cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability AssayCell Line: A375 and HT-29 Concentration: 1 nM-10 μM Incubation Time: 72 h Result: Inhibited the cell viability of A375 and HT-29 with IC 50 s of 46.5 nM and 51 nM. Western Blot AnalysisCell Line: A375 Concentration: 1, 4, 12, 37, 111, 333 and 1000 nM Incubation Time: 16 h or 0-24 h Result: Induced the reduction in the phosphorylation of ERK. Inhibited p-ERK and BRAF-V600E in a dose- and time-dependent manner. Form:Solid IC50& Target:BRAF-V600E 2 nM (Kd) Braf 2.4 nM (Kd)
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PROTAC BRAF-V600E degrader-1
CAS number:2417296-84-3 molecular formula:C48H54F2N10O10S
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| Chinese alias | PROTAC BRAF-V600E 降解剂-1 | ||
| English alias | - | ||
| CAS number | 2417296-84-3 | molecular formula | C48H54F2N10O10S |
| molecular weight | 1001.07 g/mol | Exact mass | ≥98% |
| PSA | - | logp | - |
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