Reaction Details Report a problem with these data
Target
Fibroblast growth factor receptor 3 [397-806]
Ligand
BDBM350067
Substrate
n/a
IC50
3.90±n/a nM
Citation
 Andrews, SW; Blake, JF; Cook, A; Gunawardana, IW; Hunt, KW; Metcalf, AT; Moreno, D; Ren, L; Tang, TP 2-aryl- and 2-heteroaryl-substituted 2-pyridazin-3(2H)-one compounds as inhibitors of FGFR tyrosine kinases US Patent  US10766881 Publication Date 9/8/2020 
Target
Name:
Fibroblast growth factor receptor 3 [397-806]
Synonyms:
FGFR3 | FGFR3_HUMAN | Fibroblast growth factor receptor 3 (FGFR-3) | Fibroblast growth factor receptor 3 (FGFR3) (R397-T806) | JTK4
Type:
Enzyme Catalytic Domain
Mol. Mass.:
45431.04
Organism:
Homo sapiens (Human)
Description:
P22607[397-806]
Residue:
410
Sequence:
RLRSPPKKGLGSPTVHKISRFPLKRQVSLESNASMSSNTPLVRIARLSSGEGPTLANVSELELPADPKWELSRARLTLGKPLGEGCFGQVVMAEAIGIDKDRAAKPVTVAVKMLKDDATDKDLSDLVSEMEMMKMIGKHKNIINLLGACTQGGPLYVLVEYAAKGNLREFLRARRPPGLDYSFDTCKPPEEQLTFKDLVSCAYQVARGMEYLASQKCIHRDLAARNVLVTEDNVMKIADFGLARDVHNLDYYKKTTNGRLPVKWMAPEALFDRVYTHQSDVWSFGVLLWEIFTLGGSPYPGIPVEELFKLLKEGHRMDKPANCTHDLYMIMRECWHAAPSQRPTFKQLVEDLDRVLTVTSTDEYLDLSAPFEQYSPGGQDTPSSSSSGDDSVFAHDLLPPAPPSSGGSRT
  
Inhibitor
Name:
BDBM350067
Synonyms:
US10208024, Example 66 | US10766881, Example 66
Type:
Small organic molecule
Emp. Form.:
C28H32Cl2N8O4
Mol. Mass.:
615.511
SMILES:
COCCN1CCC(CC1)n1cc(cn1)-c1cnc(N)c(n1)-c1cc(C)c(=O)n(n1)-c1c(Cl)c(OC)cc(OC)c1Cl |(-13.33,-1.72,;-12.24,-.64,;-10.75,-1.03,;-9.66,.05,;-8.17,-.34,;-7.09,.74,;-5.6,.35,;-5.2,-1.14,;-6.29,-2.23,;-7.78,-1.83,;-3.71,-1.54,;-2.81,-.29,;-1.34,-.77,;-1.34,-2.31,;-2.81,-2.79,;-.01,,;-.01,1.54,;1.32,2.31,;2.66,1.54,;3.99,2.31,;2.66,,;1.32,-.77,;3.99,-.77,;3.99,-2.31,;5.33,-3.08,;5.33,-4.62,;6.66,-2.31,;7.99,-3.08,;6.66,-.77,;5.33,,;7.99,,;9.33,-.77,;9.33,-2.31,;10.66,,;11.99,-.77,;13.33,,;10.66,1.54,;9.33,2.31,;9.33,3.85,;10.66,4.62,;7.99,1.54,;6.66,2.31,)|
Structure:
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