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Target
RAF proto-oncogene serine/threonine-protein kinase
Ligand
BDBM50237712
Substrate
n/a
Meas. Tech.
ChEMBL_470479 (CHEMBL951323)
IC50
90±n/a nM
Citation
 Zhu, T; Jiao, Y; Chen, YD; Wang, X; Li, HF; Zhang, LY; Lu, T Pharmacophore identification of Raf-1 kinase inhibitors. Bioorg Med Chem Lett 18:2346-50 (2008) [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:
BDBM50237712
Synonyms:
4-(4-(3-chlorophenyl)-2-phenyl-1H-imidazol-5-yl)pyridine | 4-[5-(3-Chloro-phenyl)-2-phenyl-3H-imidazol-4-yl]-pyridine | CHEMBL401695
Type:
Small organic molecule
Emp. Form.:
C20H14ClN3
Mol. Mass.:
331.798
SMILES:
Clc1cccc(c1)-c1[nH]c(nc1-c1ccncc1)-c1ccccc1
Structure:
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