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TargetRAF proto-oncogene serine/threonine-protein kinase [306-648,Y340D,Y341D]
LigandBDBM210021
Substrate/Competitorn/a
Meas. Tech.Raf IC50 Assay Protocol
IC50<0.250±n/a nM
Citation Zhou, CWang, SZhang, G Fused tricyclic compounds as Raf kinase inhibitors US Patent US10576087 Publication Date 3/3/2020
More Info.:Get all data from this article,  Assay Method
 
RAF proto-oncogene serine/threonine-protein kinase [306-648,Y340D,Y341D]
Name:RAF proto-oncogene serine/threonine-protein kinase [306-648,Y340D,Y341D]
Synonyms:C-Raf (Y340D/Y341D) | RAF | RAF1 | RAF1_HUMAN
Type:n/a
Mol. Mass.:38958.87
Organism:Homo sapiens (Human)
Description:PV3805, from Invitrogen
Residue:343
Sequence:
SQPKTPVPAQRERAPVSGTQEKNKIRPRGQRDSSDDWEIEASEVMLSTRIGSGSFGTVYK
GKWHGDVAVKILKVVDPTPEQFQAFRNEVAVLRKTRHVNILLFMGYMTKDNLAIVTQWCE
GSSLYKHLHVQETKFQMFQLIDIARQTAQGMDYLHAKNIIHRDMKSNNIFLHEGLTVKIG
DFGLATVKSRWSGSQQVEQPTGSVLWMAPEVIRMQDNNPFSFQSDVYSYGIVLYELMTGE
LPYSHINNRDQIIFMVGRGYASPDLSKLYKNCPKAMKRLVADCVKKVKEERPLFPQILSS
IELLQHSLPKINRSASEPSLHRAAHTEDINACTLTTSPRLPVF
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM210021
n/a
NameBDBM210021
Synonyms:US10576087, Compound 2.27 | US9273046, 2.27 | US9895376, Compound 2.27
TypeSmall organic molecule
Emp. Form.C24H18N4O4
Mol. Mass.426.4241
SMILESOc1ccc2nc([nH]c2c1)C1C2Oc3ccc(Oc4ccnc5NC(=O)CCc45)cc3C12
Structure
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