Target
Fibroblast growth factor receptor 1 [308-731]
Ligand
BDBM350007
Substrate
n/a
Meas. Tech.
LanthaScreen Assay
IC50
22.2±n/a nM
Citation
 Andrews, SWBlake, JFCook, AGunawardana, IWHunt, KWMetcalf, ATMoreno, DRen, LTang, 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 1 [308-731]
Synonyms:
BFGFR | CEK | FGFBR | FGFR1 | FGFR1_HUMAN | FLG | FLT2 | Fibroblast growth factor receptor 1 (FGFR1)(aa 308-731) | HBGFR
Type:
Enzyme Catalytic Domain
Mol. Mass.:
47326.25
Organism:
Homo sapiens (Human)
Description:
aa 308-731
Residue:
424
Sequence:
VQILKTAGVNTTDKEMEVLHLRNVSFEDAGEYTCLAGNSIGLSHHSAWLTVLEALEERPAVMTSPLYLEIIIYCTGAFLISCMVGSVIVYKMKSGTKKSDFHSQMAVHKLAKSIPLRRQVTVSADSSASMNSGVLLVRPSRLSSSGTPMLAGVSEYELPEDPRWELPRDRLVLGKPLGEGCFGQVVLAEAIGLDKDKPNRVTKVAVKMLKSDATEKDLSDLISEMEMMKMIGKHKNIINLLGACTQDGPLYVIVEYASKGNLREYLQARRPPGLEYCYNPSHNPEEQLSSKDLVSCAYQVARGMEYLASKKCIHRDLAARNVLVTEDNVMKIADFGLARDIHHIDYYKKTTNGRLPVKWMAPEALFDRIYTHQSDVWSFGVLLWEIFTLGGSPYPGVPVEELFKLLKEGHRMDKPSNCTNELYM
  
Inhibitor
Name:
BDBM350007
Synonyms:
2-(4-(5-amino-6-(1- (3,5- dimethoxyphenyl)-6- oxo-1,6- dihydropyridazin-3- yl)pyrazin-2-yl)-1H- pyrazol-1-yl)-2- methylpropanenitrile | US10208024, Example 6 | US10766881, Example 6
Type:
Small organic molecule
Emp. Form.:
C23H22N8O3
Mol. Mass.:
458.4726
SMILES:
COc1cc(OC)cc(c1)-n1nc(ccc1=O)-c1nc(cnc1N)-c1cnn(c1)C(C)(C)C#N
Structure:
Search PDB for entries with ligand similarity: