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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Adenosine receptor A3' and Ligand = 'BDBM50054682'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Adenosine receptor A3


(Homo sapiens (Human))
BDBM50054682
PNG
(2-Methyl-4-[(E)-2-(4-nitro-phenyl)-vinyl]-6-phenyl...)
Show SMILES CCO\C([O-])=C1\C(\C=C\c2ccc(cc2)[N+]([O-])=O)C(C(=[OH+])OCC)=C(C)N=C1c1ccccc1 |c:27,t:24|
Show InChI InChI=1S/C26H26N2O6/c1-4-33-25(29)22-17(3)27-24(19-9-7-6-8-10-19)23(26(30)34-5-2)21(22)16-13-18-11-14-20(15-12-18)28(31)32/h6-16,21,30H,4-5H2,1-3H3/b16-13+,26-23-
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PC cid
PC sid
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Similars

Article
PubMed
59n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Binding affinity against cloned human adenosine A3 receptor by radioligand binding assay using [125I]-AB-MECA.


J Med Chem 39: 4667-75 (1996)


Article DOI: 10.1021/jm960457c
BindingDB Entry DOI: 10.7270/Q2VQ33BG
More data for this
Ligand-Target Pair
Adenosine receptor A3


(Homo sapiens (Human))
BDBM50054682
PNG
(2-Methyl-4-[(E)-2-(4-nitro-phenyl)-vinyl]-6-phenyl...)
Show SMILES CCO\C([O-])=C1\C(\C=C\c2ccc(cc2)[N+]([O-])=O)C(C(=[OH+])OCC)=C(C)N=C1c1ccccc1 |c:27,t:24|
Show InChI InChI=1S/C26H26N2O6/c1-4-33-25(29)22-17(3)27-24(19-9-7-6-8-10-19)23(26(30)34-5-2)21(22)16-13-18-11-14-20(15-12-18)28(31)32/h6-16,21,30H,4-5H2,1-3H3/b16-13+,26-23-
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
59n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Displacement of specific [125I]-AB-MECA binding at human adenosine A3 receptor.


J Med Chem 40: 2596-608 (1997)


Article DOI: 10.1021/jm970091j
BindingDB Entry DOI: 10.7270/Q21V5D29
More data for this
Ligand-Target Pair