null

SMILES Nc1nc(OCCc2c[nH]c3ccccc23)nc2n(cnc12)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

InChI Key InChIKey=UIPASAROPWUJRQ-NVQRDWNXSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50208804   

TargetAdenosine receptor A2a(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50208804((2R,3R,4S,5R)-2-(2-(2-(1H-indol-3-yl)ethoxy)-6-ami...)copy SMILEScopy InChI
Affinity DataKi:  45nMAssay Description:Displacement of [3H]CGS-21680 from human adenosine A2A receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28916P1PubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50208804((2R,3R,4S,5R)-2-(2-(2-(1H-indol-3-yl)ethoxy)-6-ami...)copy SMILEScopy InChI
Affinity DataKi:  148nMAssay Description:Displacement of [3H]CPPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28916P1PubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50208804((2R,3R,4S,5R)-2-(2-(2-(1H-indol-3-yl)ethoxy)-6-ami...)copy SMILEScopy InChI
Affinity DataKi:  232nMAssay Description:Displacement of [125I]I-AB-MECA from human adenosine A3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28916P1PubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50208804((2R,3R,4S,5R)-2-(2-(2-(1H-indol-3-yl)ethoxy)-6-ami...)copy SMILEScopy InChI
Affinity DataEC50:  3.34E+6nMAssay Description:Agonist activity at human adenosine A2B receptor expressed in CHO cells assessed as stimulation of adenylate cyclaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2R49RNVPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50208804((2R,3R,4S,5R)-2-(2-(2-(1H-indol-3-yl)ethoxy)-6-ami...)copy SMILEScopy InChI
Affinity DataEC50:  299nMAssay Description:Agonist activity at human adenosine A2B receptor expressed in CHO cells assessed as stimulation of cAMP productionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28916P1PubMed