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BDBM50246774 3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyrrolo[3',4':2,3][1,4]diazepino[1,7-a]indol-2-yl)propyl Imidothiocarbamate::CHEMBL489083

SMILES: NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O

InChI Key: InChIKey=RUTCIZOQGCWURK-UHFFFAOYSA-N

Data: 16 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 16 hits for monomerid = 50246774   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Focal adhesion kinase 1/vascular endothelial growth factor receptor 3


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 4.70E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human VEGFR3


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Tyrosine-protein kinase receptor UFO


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 4.40E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human AXL


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 9.00E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human AKT1


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 2


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 3.60E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human CDK2/Cyc2


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 4


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 2.70E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human CDK4/CycD1


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Hepatocyte growth factor receptor


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 3.30E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human MET


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Platelet-derived growth factor receptor beta


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 4.20E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human PDGFRbeta


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PLK1


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 9.90E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human PLK1


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 3.80E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human SRC


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 4.60E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human EGFR


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Ephrin type-B receptor 4


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 2.30E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human EPHB4


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Receptor tyrosine-protein kinase erbB-2


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 7.70E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human ERBB2


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Focal adhesion kinase 1


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 4.40E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human FAK


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Insulin-like growth factor I receptor


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 4.00E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human IGF1R


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 4.10E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human VEGFR2


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50246774
PNG
(3-(1,3-Dioxo-1,3-dihydro-2H-indolo[1',7':4,5,6]pyr...)
Show SMILES NC(=N)SCCCn1c(=O)c2c(n3c(cc4ccccc34)c3cccc4ccn2c34)c1=O
Show InChI InChI=1S/C24H19N5O2S/c25-24(26)32-12-4-10-28-22(30)20-21(23(28)31)29-17-8-2-1-5-15(17)13-18(29)16-7-3-6-14-9-11-27(20)19(14)16/h1-3,5-9,11,13H,4,10,12H2,(H3,25,26)
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n/an/a 2.60E+3n/an/an/an/an/an/a



Institute of General Genetics

Curated by ChEMBL


Assay Description
Inhibition of human INSR


J Med Chem 51: 7731-6 (2008)


Article DOI: 10.1021/jm800758s
BindingDB Entry DOI: 10.7270/Q2HD7VH4
More data for this
Ligand-Target Pair