B-Raf IN 19 is a specific BRAF inhibitor targeting both BRAF wild-type (BRAF WT) and BRAF V600E mutants, with IC50 values of 0.57 μM and 0.28 μM, respectively. This compound effectively disrupts MAPK signaling pathways in melanoma cells, making it a valuable tool for research focused on cancer signaling mechanisms and therapeutic interventions in melanoma. Its selective inhibition profile supports its use in studies aimed at understanding BRAF-related oncogenic processes.
B-Raf IN 19 is a specific BRAF inhibitor targeting both BRAF wild-type (BRAF WT) and BRAF V600E mutants, with IC50 values of 0.57 μM and 0.28 μM, respectively. This compound effectively disrupts MAPK signaling pathways in melanoma cells, making it a valuable tool for research focused on cancer signaling mechanisms and therapeutic interventions in melanoma. Its selective inhibition profile supports its use in studies aimed at understanding BRAF-related oncogenic processes.
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