null

SMILES Nc1c(cc(Nc2ccc(Nc3ncccn3)c(c2)S([O-])(=O)=O)c2C(=O)c3ccccc3C(=O)c12)S([O-])(=O)=O

InChI Key InChIKey=ZIFQNSIXEIWWPD-UHFFFAOYSA-L

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50268965   

TargetP2Y purinoceptor 12(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50268965(CHEMBL499428 | Disodium 1-amino-4-[4-([1,3]diazine...)copy SMILEScopy InChI
Affinity DataKi:  50.7nMAssay Description:Displacement of [3H]PSB0413 from human platelet P2Y12 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3FZFPubMed
TargetP2X purinoceptor 2(RAT)
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50268965(CHEMBL499428 | Disodium 1-amino-4-[4-([1,3]diazine...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity against rat P2X2 receptor expressed in Xenopus laevis oocyte assessed as inhibition of alpha, beta-meATP-induced inward current b...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PTGPubMed
TargetP2X purinoceptor 4(RAT)
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50268965(CHEMBL499428 | Disodium 1-amino-4-[4-([1,3]diazine...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Antagonist activity against rat P2X4 receptor expressed in Xenopus laevis oocyte assessed as inhibition of alpha, beta-meATP-induced inward current b...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PTGPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50268965(CHEMBL499428 | Disodium 1-amino-4-[4-([1,3]diazine...)copy SMILEScopy InChI
Affinity DataIC50: 760nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cells assessed as ratio of IC50 in presence of GTP to absence of GTP by G...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3FZFPubMed