General Information of the Compound
Compound ID
CP0007142
Compound Name
N-[3-chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[5-[(2-methylsulfonylethylamino)methyl]furan-2-yl]quinazolin-4-amine
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Synonyms
4-[[3-Chloro-4-(3-fluorobenzyloxy)phenyl]amino]-6-[5-[[(2-methanesulfonylethyl)amino]methyl]furan-2-yl]quinazoline
FMM
GSK 572016
GSK572016
GW 572016
GW 572016X
GW572016
Lapatinib
Lapatinib (ERBB2 inhibitor)
Lapatinib (INN)
Lapatinib Ditosylate
Lapatinib [INN]
Lapatinib tosilate hydrate
Lapatinib, Tykerb, GW572016
N-(3-Chloro-4-((3-fluorophenyl)methoxy)phenyl)-6-(5-((2-methylsulfonylethylamino)methyl)-2-furyl)quinazolin-4-amine
N-(3-Chloro-4-{[(3-fluorophenyl)methyl]oxy}phenyl)-6-[5-({[2-(methylsulfonyl)ethyl]amino}methyl)-2-furanyl]-4-quinazolinamine
N-[3-chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[5-[(2-methylsulfonylethylamino)methyl]furan-2-yl]quinazolin-4-amine
N-{3-CHLORO-4-[(3-FLUOROBENZYL)OXY]PHENYL}-6-[5-({[2-(METHYLSULFONYL)ETHYL]AMINO}METHYL)-2-FURYL]-4-QUINAZOLINAMINE
Tycerb
Tykerb (TN)
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Structure
Formula
C29H26ClFN4O4S
Molecular Weight
581.069
Canonical SMILES
CS(=O)(=O)CCNCc1ccc(o1)-c1ccc2ncnc(Nc3ccc(OCc4cccc(F)c4)c(Cl)c3)c2c1
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InChI
InChI=1S/C29H26ClFN4O4S/c1-40(36,37)12-11-32-16-23-7-10-27(39-23)20-5-8-26-24(14-20)29(34-18-33-26)35-22-6-9-28(25(30)15-22)38-17-19-3-2-4-21(31)13-19/h2-10,13-15,18,32H,11-12,16-17H2,1H3,(H,33,34,35)
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InChIKey
BCFGMOOMADDAQU-UHFFFAOYSA-N
CAS
231277-92-2
Physicochemical Property
logP
6.1391
Rotatable Bonds
11
Heavy Atom Count
40
Polar Areas
106.35
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
8
Complexity
40

"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: 208908
SID: 14911387
ChEMBL ID
CHEMBL554
DrugBank ID
DB01259
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
CL000013 Sf9 Spodoptera frugiperda (Fall armyworm)  3
1
IC50 = 0.06 nM
   TI
   LI
   LO
   TS
2
IC50 = 0.2 nM
   TI
   LI
   LO
   TS
3
IC50 = 24 nM
   TI
   LI
   LO
   TS
CL000012 Sf21 Spodoptera frugiperda (Fall armyworm)  3
1
IC50 = 21 nM
   TI
   LI
   LO
   TS
2
IC50 = 224.89 nM
   TI
   LI
   LO
   TS
3
IC50 > 5000 nM
   TI
   LI
   LO
   TS
CL000052 A-431 Homo sapiens (Human)  3
1
IC50 = 21 nM
   TI
   LI
   LO
   TS
2
IC50 = 52 nM
   TI
   LI
   LO
   TS
3
IC50 = 2685 nM
   TI
   LI
   LO
   TS
CL000063 Hep-G2 Homo sapiens (Human)  1
1
IC50 = 27.1 nM
   TI
   LI
   LO
   TS
CL000217 CAL-27 Homo sapiens (Human)  1
1
IC50 < 32 nM
   TI
   LI
   LO
   TS
CL000220 KB Homo sapiens (Human)  1
1
IC50 = 62 nM
   TI
   LI
   LO
   TS
CL000215 MiaPaCa(BCRP) Homo sapiens (Human)  1
1
IC50 = 433 nM
   TI
   LI
   LO
   TS
CL000157 NCI-H1975 Homo sapiens (Human)  1
1
IC50 = 14781 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 2.9 nM
2 IC50 = 3 nM
3 IC50 = 5.5 nM
4 IC50 = 7.9 nM
5 IC50 = 8 nM
6 IC50 = 8.9 nM
7 IC50 = 9 nM
8 IC50 = 10 nM
9 IC50 = 10.2 nM
10 IC50 = 10.8 nM
11 IC50 = 11 nM
12 IC50 = 11.2 nM
13 IC50 = 12 nM
14 IC50 = 13.42 nM
15 IC50 = 15 nM
16 IC50 = 17 nM
17 IC50 = 22 nM
18 IC50 = 27.06 nM
19 IC50 = 46 nM
20 IC50 = 52 nM
21 IC50 = 52.2 nM
22 IC50 = 280 nM
23 IC50 = 61060 nM
24 IC50 > 4000 nM
25 Kd = 0.92 nM
26 Kd = 1.2 nM
27 Kd = 2.1 nM
28 Kd = 2.2 nM
29 Kd = 2.4 nM
30 Kd = 2.8 nM
31 Kd = 3.5 nM
32 Kd = 3.9 nM
33 Kd = 4.2 nM
34 Kd = 5.5 nM
35 Kd = 8.6 nM
36 Kd = 860 nM
37 Kd > 10000 nM
38 Ki = 3 nM
Protein ID: PT00991, Histone deacetylase 1
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
IC50 > 10000 nM
   TI
   LI
   LO
   TS
Protein ID: PT00995, Histone deacetylase 3
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000012 Sf21 Spodoptera frugiperda (Fall armyworm)  1
1
IC50 > 10000 nM
   TI
   LI
   LO
   TS
Protein ID: PT01213, Histone deacetylase 6
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
IC50 > 10000 nM
   TI
   LI
   LO
   TS
Protein ID: PT01499, Histone deacetylase 8
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000012 Sf21 Spodoptera frugiperda (Fall armyworm)  1
1
IC50 > 10000 nM
   TI
   LI
   LO
   TS
Protein ID: PT01104, Insulin-like growth factor 1 receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000052 A-431 Homo sapiens (Human)  1
1
IC50 > 10000 nM
   TI
   LI
   LO
   TS
CL000215 MiaPaCa(BCRP) Homo sapiens (Human)  1
1
IC50 > 30000 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 Kd > 10000 nM
Protein ID: PT01092, Platelet-derived growth factor receptor alpha
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000013 Sf9 Spodoptera frugiperda (Fall armyworm)  1
1
IC50 > 20000 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 Kd > 10000 nM
Protein ID: PT01233, Receptor tyrosine-protein kinase erbB-2
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000013 Sf9 Spodoptera frugiperda (Fall armyworm)  1
1
IC50 = 2.8 nM
   TI
   LI
   LO
   TS
CL000216 NCI-N87 Homo sapiens (Human)  1
1
IC50 = 100 nM
   TI
   LI
   LO
   TS
CL000218 BT-474 Homo sapiens (Human)  1
1
IC50 = 140 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 2.7 nM
2 IC50 = 4.5 nM
3 IC50 = 9 nM
4 IC50 = 9.2 nM
5 IC50 = 9.8 nM
6 IC50 = 10 nM
7 IC50 = 10.2 nM
8 IC50 = 10.3 nM
9 IC50 = 13 nM
10 IC50 = 23.9 nM
11 IC50 = 29.2 nM
12 IC50 = 36 nM
13 IC50 = 36.3 nM
14 IC50 = 42 nM
15 IC50 = 60 nM
16 IC50 = 95.5 nM
17 IC50 = 540 nM
18 Kd = 7 nM
19 Kd = 11 nM
Cell Viability or Cytotoxicity Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000017 HeLa Homo sapiens (Human)  1
1
IC50 = 5900 nM
   TI
   LI
   LO
   TS
CL000052 A-431 Homo sapiens (Human)  2
1
IC50 = 3590 nM
   TI
   LI
   LO
   TS
2
IC50 = 4800 nM
   TI
   LI
   LO
   TS
CL000063 Hep-G2 Homo sapiens (Human)  1
1
IC50 = 11710 nM
   TI
   LI
   LO
   TS
CL000068 A-549 Homo sapiens (Human)  1
1
IC50 = 14900 nM
   TI
   LI
   LO
   TS
CL000083 MCF-7 Homo sapiens (Human)  1
1
IC50 = 5020 nM
   TI
   LI
   LO
   TS
CL000157 NCI-H1975 Homo sapiens (Human)  1
1
IC50 = 12680 nM
   TI
   LI
   LO
   TS
CL000216 NCI-N87 Homo sapiens (Human)  1
1
IC50 = 53 nM
   TI
   LI
   LO
   TS
CL000217 CAL-27 Homo sapiens (Human)  1
1
IC50 = 7 nM
   TI
   LI
   LO
   TS
CL000261 SK-BR-3 Homo sapiens (Human)  1
1
IC50 = 2 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( Lapatinib )
Drug Name Lapatinib
Company GlaxoSmithKline
Indication
Breast cancer
Approved
Target(s)
Eukaryotic elongation factor 2 kinase (eEF-2K)
Inhibitor
Epidermal growth factor receptor (EGFR)
Inhibitor
Erbb2 tyrosine kinase receptor (HER2)
Inhibitor