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BDBM50215928 4-(4-bromo-1H-pyrrol-2-yl)-1H-imidazo[4,5-c]pyridin-2-amine::CHEMBL231012

SMILES: Nc1nc2c(nccc2[nH]1)-c1cc(Br)c[nH]1

InChI Key: InChIKey=PZVQODCOQPBJAM-UHFFFAOYSA-N

Data: 2 IC50

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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50215928   
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
Matrix metalloproteinase-12 (MMP12)


(Homo sapiens (Human))
BDBM50215928
PNG
(4-(4-bromo-1H-pyrrol-2-yl)-1H-imidazo[4,5-c]pyridi...)
Show SMILES Nc1nc2c(nccc2[nH]1)-c1cc(Br)c[nH]1
Show InChI InChI=1S/C10H8BrN5/c11-5-3-7(14-4-5)8-9-6(1-2-13-8)15-10(12)16-9/h1-4,14H,(H3,12,15,16)
PDB
MMDB

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PC cid
PC sid
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Similars

Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human MMP12 catalytic domain


Bioorg Med Chem Lett 19: 5461-3 (2009)


Article DOI: 10.1016/j.bmcl.2009.07.099
BindingDB Entry DOI: 10.7270/Q2HX1CRC
More data for this
Ligand-Target Pair
Matrix metalloproteinase-12 (MMP12)


(Homo sapiens (Human))
BDBM50215928
PNG
(4-(4-bromo-1H-pyrrol-2-yl)-1H-imidazo[4,5-c]pyridi...)
Show SMILES Nc1nc2c(nccc2[nH]1)-c1cc(Br)c[nH]1
Show InChI InChI=1S/C10H8BrN5/c11-5-3-7(14-4-5)8-9-6(1-2-13-8)15-10(12)16-9/h1-4,14H,(H3,12,15,16)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



Kyorin Pharmaceutical Co. Ltd

Curated by ChEMBL


Assay Description
Inhibition of MMP12


Bioorg Med Chem Lett 17: 4495-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.06.005
BindingDB Entry DOI: 10.7270/Q2MW2GVX
More data for this
Ligand-Target Pair