Target
RAF proto-oncogene serine/threonine-protein kinase [325-648]
Ligand
BDBM202698
Substrate
n/a
Meas. Tech.
In Vitro Activity Assay
IC50
0.714±n/a nM
Citation
 Aversa, RJBarsanti, PABurger, MTDillon, MPDipesa, AHu, CLou, YNishiguchi, GAPan, YPolyakov, VRRamurthy, SRico, ACSetti, LQSmith, ASubramanian, STaft, BRTanner, HRWan, LYusuff, N Biaryl amide compounds as kinase inhibitors US Patent  US10709712 Publication Date 7/14/2020 
Target
Name:
RAF proto-oncogene serine/threonine-protein kinase [325-648]
Synonyms:
RAF | RAF proto-oncogene serine/threonine-protein kinase (truncated)(325-648) | RAF1 | RAF1_HUMAN
Type:
Enzyme Catalytic Domain
Mol. Mass.:
37066.83
Organism:
Homo sapiens (Human)
Description:
aa 325-648, C-Raf TR refers to a truncated
Residue:
324
Sequence:
QEKNKIRPRGQRDSSYYWEIEASEVMLSTRIGSGSFGTVYKGKWHGDVAVKILKVVDPTPEQFQAFRNEVAVLRKTRHVNILLFMGYMTKDNLAIVTQWCEGSSLYKHLHVQETKFQMFQLIDIARQTAQGMDYLHAKNIIHRDMKSNNIFLHEGLTVKIGDFGLATVKSRWSGSQQVEQPTGSVLWMAPEVIRMQDNNPFSFQSDVYSYGIVLYELMTGELPYSHINNRDQIIFMVGRGYASPDLSKLYKNCPKAMKRLVADCVKKVKEERPLFPQILSSIELLQHSLPKINRSASEPSLHRAAHTEDINACTLTTSPRLPVF
  
Inhibitor
Name:
BDBM202698
Synonyms:
US10245267, Example 44 | US10709712, Example 44 | US9242969, 44 | US9694016, 44
Type:
Small organic molecule
Emp. Form.:
C26H27F3N4O2
Mol. Mass.:
484.5134
SMILES:
CC(C)c1cc(nc(n1)-c1cc(NC(=O)c2cccc(c2)C(F)(F)F)ccc1C)N1CCOCC1
Structure:
Search PDB for entries with ligand similarity: