BDBM50300129 CHEMBL572528::CIBACRON BLUE::Cibacron Blue 3Ga

SMILES c1ccc2c(c1)C(=O)c3c(cc(c(c3C2=O)N)S(=O)(=O)O)Nc4ccc(c(c4)S(=O)(=O)O)Nc5nc(nc(n5)Cl)Nc6ccccc6S(=O)(=O)O

InChI Key InChIKey=YKCWQPZFAFZLBI-UHFFFAOYSA-N

Data  5 KI  1 IC50

PDB links: 5 PDB IDs match this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50300129   

TargetHematopoietic prostaglandin D synthase(Human)
The University of Queensland

Curated by ChEMBL
LigandPNGBDBM50300129(CHEMBL572528 | Cibacron Blue 3Ga | CIBACRON BLUE)
Affinity DataIC50: 200nMAssay Description:Inhibition of human H-PGDS expressed in Escherichia coli BL21 assessed as rate of glutathione-chloro-dinitro benzene conjugationMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetP2X purinoceptor 4(Human)
Max-Planck Institute For Experimental Medicine

Curated by PDSP Ki Database
LigandPNGBDBM50300129(CHEMBL572528 | Cibacron Blue 3Ga | CIBACRON BLUE)
Affinity DataKi:  39.2nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/24/2012
Entry Details Article
PubMed
TargetP2X purinoceptor 4(Rat)
Max-Planck Institute For Experimental Medicine

Curated by PDSP Ki Database
LigandPNGBDBM50300129(CHEMBL572528 | Cibacron Blue 3Ga | CIBACRON BLUE)
Affinity DataKi:  128nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/24/2012
Entry Details Article
PubMed
TargetP2X purinoceptor 2(Human)
Abbott Laboratories

Curated by PDSP Ki Database
LigandPNGBDBM50300129(CHEMBL572528 | Cibacron Blue 3Ga | CIBACRON BLUE)
Affinity DataKi:  800nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2012
Entry Details Article
PubMed
TargetP2X purinoceptor 3(Human)
Abbott Laboratories

Curated by PDSP Ki Database
LigandPNGBDBM50300129(CHEMBL572528 | Cibacron Blue 3Ga | CIBACRON BLUE)
Affinity DataKi:  2.53E+3nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2012
Entry Details Article
PubMed
TargetIntegrase(Human immunodeficiency virus type 1)
University of Newcastle

Curated by ChEMBL
LigandPNGBDBM50300129(CHEMBL572528 | Cibacron Blue 3Ga | CIBACRON BLUE)
Affinity DataKi:  2.90E+3nMAssay Description:Binding affinity to influenza A/Beijing/262/95 H1N1 neuraminidase expressed in baculovirus expression system using sialyl-lactose as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/21/2023
Entry Details
PubMed