Target
RAF proto-oncogene serine/threonine-protein kinase
Ligand
BDBM50085416
Substrate
n/a
Meas. Tech.
ChEBML_217655
IC50
65±n/a nM
Citation
 Lackey, KCory, MDavis, RFrye, SVHarris, PAHunter, RNJung, DKMcDonald, OBMcNutt, RWPeel, MRRutkowske, RDVeal, JMWood, ER The discovery of potent cRaf1 kinase inhibitors. Bioorg Med Chem Lett 10:223-6 (2000) [PubMed]  Article 
Target
Name:
RAF proto-oncogene serine/threonine-protein kinase
Synonyms:
C-Raf Protein Kinase | Proto-oncogene c-RAF (RAF1) | RAF | RAF proto-oncogene serine/threonine-protein kinase (C-Raf) | RAF1 | RAF1_HUMAN | Raf-1 | Serine/threonine-protein kinase RAF | Serine/threonine-protein kinase C-Raf | cRaf
Type:
Serine/threonine-protein kinase
Mol. Mass.:
73082.52
Organism:
Homo sapiens (Human)
Description:
P04049
Residue:
648
Sequence:
MEHIQGAWKTISNGFGFKDAVFDGSSCISPTIVQQFGYQRRASDDGKLTDPSKTSNTIRVFLPNKQRTVVNVRNGMSLHDCLMKALKVRGLQPECCAVFRLLHEHKGKKARLDWNTDAASLIGEELQVDFLDHVPLTTHNFARKTFLKLAFCDICQKFLLNGFRCQTCGYKFHEHCSTKVPTMCVDWSNIRQLLLFPNSTIGDSGVPALPSLTMRRMRESVSRMPVSSQHRYSTPHAFTFNTSSPSSEGSLSQRQRSTSTPNVHMVSTTLPVDSRMIEDAIRSHSESASPSALSSSPNNLSPTGWSQPKTPVPAQRERAPVSGTQEKNKIRPRGQRDSSYYWEIEASEVMLSTRIGSGSFGTVYKGKWHGDVAVKILKVVDPTPEQFQAFRNEVAVLRKTRHVNILLFMGYMTKDNLAIVTQWCEGSSLYKHLHVQETKFQMFQLIDIARQTAQGMDYLHAKNIIHRDMKSNNIFLHEGLTVKIGDFGLATVKSRWSGSQQVEQPTGSVLWMAPEVIRMQDNNPFSFQSDVYSYGIVLYELMTGELPYSHINNRDQIIFMVGRGYASPDLSKLYKNCPKAMKRLVADCVKKVKEERPLFPQILSSIELLQHSLPKINRSASEPSLHRAAHTEDINACTLTTSPRLPVF
  
Inhibitor
Name:
BDBM50085416
Synonyms:
5-(2-Chloro-acetyl)-3-[1-(3,5-dibromo-4-hydroxy-phenyl)-meth-(Z)-ylidene]-1,3-dihydro-indol-2-one | CHEMBL72179
Type:
Small organic molecule
Emp. Form.:
C17H10Br2ClNO3
Mol. Mass.:
471.527
SMILES:
Oc1c(Br)cc(C=C2C(=O)Nc3ccc(cc23)C(=O)CCl)cc1Br |w:6.5|
Structure:
Search PDB for entries with ligand similarity: