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SMILES: O=c1[nH]nc(-c2ccnc(Nc3nccs3)c2)n1-c1ccc2ccccc2c1

InChI Key: InChIKey=NDINXVZGAZZFMK-UHFFFAOYSA-N

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 5 hits for monomerid = 50333991   
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
Mitogen-activated protein kinase 10


(Homo sapiens (Human))
BDBM50333991
PNG
(4-(naphthalen-2-yl)-3-(2-(thiazol-2-ylamino)pyridi...)
Show SMILES O=c1[nH]nc(-c2ccnc(Nc3nccs3)c2)n1-c1ccc2ccccc2c1
Show InChI InChI=1S/C20H14N6OS/c27-20-25-24-18(15-7-8-21-17(12-15)23-19-22-9-10-28-19)26(20)16-6-5-13-3-1-2-4-14(13)11-16/h1-12H,(H,25,27)(H,21,22,23)
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n/an/a 210n/an/an/an/an/an/a



Elan Pharmaceuticals

Curated by ChEMBL


Assay Description
Inhibition of recombinant JNK3 after 60 mins by TR-FRET assay


Bioorg Med Chem Lett 21: 315-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.11.010
BindingDB Entry DOI: 10.7270/Q24F1R0T
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 9


(Homo sapiens (Human))
BDBM50333991
PNG
(4-(naphthalen-2-yl)-3-(2-(thiazol-2-ylamino)pyridi...)
Show SMILES O=c1[nH]nc(-c2ccnc(Nc3nccs3)c2)n1-c1ccc2ccccc2c1
Show InChI InChI=1S/C20H14N6OS/c27-20-25-24-18(15-7-8-21-17(12-15)23-19-22-9-10-28-19)26(20)16-6-5-13-3-1-2-4-14(13)11-16/h1-12H,(H,25,27)(H,21,22,23)
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n/an/a 650n/an/an/an/an/an/a



Elan Pharmaceuticals

Curated by ChEMBL


Assay Description
Inhibition of recombinant JNK2 after 60 mins by TR-FRET assay


Bioorg Med Chem Lett 21: 315-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.11.010
BindingDB Entry DOI: 10.7270/Q24F1R0T
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50333991
PNG
(4-(naphthalen-2-yl)-3-(2-(thiazol-2-ylamino)pyridi...)
Show SMILES O=c1[nH]nc(-c2ccnc(Nc3nccs3)c2)n1-c1ccc2ccccc2c1
Show InChI InChI=1S/C20H14N6OS/c27-20-25-24-18(15-7-8-21-17(12-15)23-19-22-9-10-28-19)26(20)16-6-5-13-3-1-2-4-14(13)11-16/h1-12H,(H,25,27)(H,21,22,23)
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n/an/a>5.00E+4n/an/an/an/an/an/a



Elan Pharmaceuticals

Curated by ChEMBL


Assay Description
Inhibition of recombinant p38alpha after 60 mins by TR-FRET assay


Bioorg Med Chem Lett 21: 315-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.11.010
BindingDB Entry DOI: 10.7270/Q24F1R0T
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Homo sapiens (Human))
BDBM50333991
PNG
(4-(naphthalen-2-yl)-3-(2-(thiazol-2-ylamino)pyridi...)
Show SMILES O=c1[nH]nc(-c2ccnc(Nc3nccs3)c2)n1-c1ccc2ccccc2c1
Show InChI InChI=1S/C20H14N6OS/c27-20-25-24-18(15-7-8-21-17(12-15)23-19-22-9-10-28-19)26(20)16-6-5-13-3-1-2-4-14(13)11-16/h1-12H,(H,25,27)(H,21,22,23)
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n/an/a>5.00E+4n/an/an/an/an/an/a



Elan Pharmaceuticals

Curated by ChEMBL


Assay Description
Inhibition of recombinant ERK2 after 60 mins by TR-FRET assay


Bioorg Med Chem Lett 21: 315-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.11.010
BindingDB Entry DOI: 10.7270/Q24F1R0T
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 8


(Homo sapiens (Human))
BDBM50333991
PNG
(4-(naphthalen-2-yl)-3-(2-(thiazol-2-ylamino)pyridi...)
Show SMILES O=c1[nH]nc(-c2ccnc(Nc3nccs3)c2)n1-c1ccc2ccccc2c1
Show InChI InChI=1S/C20H14N6OS/c27-20-25-24-18(15-7-8-21-17(12-15)23-19-22-9-10-28-19)26(20)16-6-5-13-3-1-2-4-14(13)11-16/h1-12H,(H,25,27)(H,21,22,23)
PDB
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PC sid
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Article
PubMed
n/an/a>5.00E+4n/an/an/an/an/an/a



Elan Pharmaceuticals

Curated by ChEMBL


Assay Description
Inhibition of recombinant JNK1 after 60 mins by TR-FRET assay


Bioorg Med Chem Lett 21: 315-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.11.010
BindingDB Entry DOI: 10.7270/Q24F1R0T
More data for this
Ligand-Target Pair