BDBM209864 2-[(1R)-1-[(6-amino-5-chloropyrimidine-4-carbonyl)amino]ethyl]-N-[5-chloro-4-(trifluoromethyl)pyridin-2-yl]-1,3-thiazole-5-carboxamide::MLN-2480
SMILES C[C@H](c1ncc(s1)C(=O)Nc2cc(c(cn2)Cl)C(F)(F)F)NC(=O)c3c(c(ncn3)N)Cl
InChI Key InChIKey=VWMJHAFYPMOMGF-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 5 hits for monomerid = 209864
TargetRAF proto-oncogene serine/threonine-protein kinase(Human)
University of Sharjah
Curated by ChEMBL
University of Sharjah
Curated by ChEMBL
Affinity DataIC50: 94nMAssay Description:Inhibition of wild type C-RAF (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 94nMAssay Description:Inhibition of B-RAF V600E mutant (unknown origin)More data for this Ligand-Target Pair
Affinity DataKd: 484nMAssay Description:Kinobeads competition assays were performed in 96-well format as previously described using mixed protein lysates of four cancer cell lines (K-562, M...More data for this Ligand-Target Pair
TargetRAF proto-oncogene serine/threonine-protein kinase(Human)
University of Sharjah
Curated by ChEMBL
University of Sharjah
Curated by ChEMBL
Affinity DataIC50: 495nMAssay Description:Inhibition of RAF1 Y340D (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 633nMAssay Description:Inhibition of wild-type B-RAF (unknown origin)More data for this Ligand-Target Pair

3D Structure (crystal)