General Information of the Compound
Compound ID
CP0240838
Compound Name
N-[7-chloro-1-[(3R)-1-[(E)-4-(dimethylamino)but-2-enoyl]azepan-3-yl]benzimidazol-2-yl]-2-methylpyridine-4-carboxamide
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Synonyms
EGF816
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Structure
Formula
C26H31ClN6O2
Molecular Weight
495.027
Canonical SMILES
CN(C)C\C=C\C(=O)N1CCCC[C@H](C1)n1c(NC(=O)c2ccnc(C)c2)nc2cccc(Cl)c12
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InChI
InChI=1S/C26H31ClN6O2/c1-18-16-19(12-13-28-18)25(35)30-26-29-22-10-6-9-21(27)24(22)33(26)20-8-4-5-15-32(17-20)23(34)11-7-14-31(2)3/h6-7,9-13,16,20H,4-5,8,14-15,17H2,1-3H3,(H,29,30,35)/b11-7+/t20-/m1/s1
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InChIKey
IOMMMLWIABWRKL-WUTDNEBXSA-N
CAS
1508250-71-2
Physicochemical Property
logP
4.31682
Rotatable Bonds
6
Heavy Atom Count
35
Polar Areas
83.36
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
6
Complexity
35

"RO5" indicates the cutoff set by lipinski's rule of five:

(1) Molecular weight less than 500 Dalton;

(2) xlogp less than 5;

(3) No more than 5 hbonddonor (Hydrogen Bond Donor Count);

(4) No more than 10 hbondacc (Hydrogen Bond Acceptor Count);

(5) No more than 10 rotbonds (Rotatable Bond Count).

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PubChem ID
CID: 72703790
ChEMBL ID
CHEMBL3787344
DrugBank ID
DB16250
Map of Molecular Bioactivity Related to the Compound
Map of Molecular Bioactivity Related to the Compound

Compound
Cell Line
Protein

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Compound
Protein ID: PT00922, Epidermal growth factor receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000157 NCI-H1975 Homo sapiens (Human)  1
1
IC50 = 4.18 nM
   TI
   LI
   LO
   TS
CL000324 NCI-H3255 Homo sapiens (Human)  1
1
IC50 = 6.11 nM
   TI
   LI
   LO
   TS
CL000150 HaCaT Homo sapiens (Human)  1
1
IC50 = 160.6 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( EGF816 )
Drug Name EGF816
Company Novartis pharmaceuticals
Indication
Non-small-cell lung cancer
Phase 3
Non-small-cell lung cancer
Phase 1/2
Target(s)
Epidermal growth factor receptor (EGFR)
Inhibitor