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TargetEpidermal growth factor receptor [695-1022]
LigandBDBM525525
Substrate/Competitorn/a
Meas. Tech.Biochemical EGFR Inhibition Assays (5 mM ATP)
IC50 179±n/a nM
Citation Boese, DDahmann, GEngelhardt, HPetronczki, MScharn, D Benzimidazole compounds and derivatives as EGFR inhibitors US Patent US11174245 Publication Date 11/16/2021
More Info.:Get all data from this article,  Assay Method
 
Epidermal growth factor receptor [695-1022]
Name:Epidermal growth factor receptor [695-1022]
Synonyms:EGFR | EGFR (aa 695-1022) | EGFR_HUMAN | ERBB | ERBB1 | HER1
Type:Enzyme Catalytic Domain
Mol. Mass.:37339.79
Organism:Homo sapiens (Human)
Description:P00533[695-1022]
Residue:328
Sequence:
SGEAPNQALLRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEKVKIPVAIKELREATSPK
ANKEILDEAYVMASVDNPHVCRLLGICLTSTVQLITQLMPFGCLLDYVREHKDNIGSQYL
LNWCVQIAKGMNYLEDRRLVHRDLAARNVLVKTPQHVKITDFGLAKLLGAEEKEYHAEGG
KVPIKWMALESILHRIYTHQSDVWSYGVTVWELMTFGSKPYDGIPASEISSILEKGERLP
QPPICTIDVYMIMVKCWMIDADSRPKFRELIIEFSKMARDPQRYLVIQGDERMHLPSPTD
SNFYRALMDEEDMDDVVDADEYLIPQQG
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  Blast E-value cutoff:
BDBM525525
n/a
NameBDBM525525
Synonyms:US11174245, # I-203
TypeSmall organic molecule
Emp. Form.C23H23ClN6O2
Mol. Mass.450.921
SMILESCn1ncc(c1Cl)-c1cc(ccn1)C(=O)\N=c1/[nH]c2ccccc2n1[C@@H]1CC[C@H](O)CC1 |r,wU:25.28,28.32,(5.75,-2.98,;5.75,-1.44,;6.99,-.53,;6.52,.93,;4.98,.93,;4.5,-.53,;3.17,-1.3,;4.21,2.26,;2.67,2.26,;1.9,3.6,;2.67,4.93,;4.21,4.93,;4.98,3.6,;.36,3.6,;-.41,4.93,;-.41,2.26,;-1.95,2.26,;-2.86,3.51,;-4.32,3.03,;-5.66,3.8,;-6.99,3.03,;-6.99,1.49,;-5.66,.72,;-4.32,1.49,;-2.86,1.02,;-2.46,-.47,;-3.55,-1.56,;-3.15,-3.05,;-1.66,-3.44,;-1.27,-4.93,;-.57,-2.36,;-.97,-.87,)|
Structure
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