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SMILES Nc1nc2n(CCCc3ccc4OCOc4c3)ncc2c2nc(nn12)-c1ccco1

InChI Key InChIKey=ULSNKDYWRFKLBP-UHFFFAOYSA-N

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50064696   

TargetAdenosine receptor A2a(Homo sapiens (Human))
Universit£ di Padova

Curated by ChEMBL
LigandPNGBDBM50064696(7-(3-(benzo[d][1,3]dioxol-5-yl)propyl)-2-(furan-2-...)copy SMILEScopy InChI
Affinity DataKi:  3.30nMAssay Description:Displacement of [3H]NECA from human adenosine A2A receptor expressed in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23FXPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Universit£ di Padova

Curated by ChEMBL
LigandPNGBDBM50064696(7-(3-(benzo[d][1,3]dioxol-5-yl)propyl)-2-(furan-2-...)copy SMILEScopy InChI
Affinity DataKi:  3.30nMAssay Description:Displacement of [3H]-SCH- 58261 from human Adenosine A2A receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2251H9KPubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Università di Ferrara

Curated by ChEMBL
LigandPNGBDBM50064696(7-(3-(benzo[d][1,3]dioxol-5-yl)propyl)-2-(furan-2-...)copy SMILEScopy InChI
Affinity DataKi:  3.80nMAssay Description:Displacement of [3H]-CGS- 21680 from rat striatal membranes Adenosine A2A receptor. Parenthesis indicate 95% confidence limits.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2251H9KPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Università di Ferrara

Curated by ChEMBL
LigandPNGBDBM50064696(7-(3-(benzo[d][1,3]dioxol-5-yl)propyl)-2-(furan-2-...)copy SMILEScopy InChI
Affinity DataKi:  1.84E+3nMAssay Description:Displacement of [3H]-CHA from rat cortical membrane Adenosine A1 receptor. Parenthesis indicate 95% confidence limit.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2251H9KPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Università di Ferrara

Curated by ChEMBL
LigandPNGBDBM50064696(7-(3-(benzo[d][1,3]dioxol-5-yl)propyl)-2-(furan-2-...)copy SMILEScopy InChI
Affinity DataKi:  2.17E+3nMAssay Description:Displacement of [3H]-CHA from human Adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2251H9KPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Universit£ di Padova

Curated by ChEMBL
LigandPNGBDBM50064696(7-(3-(benzo[d][1,3]dioxol-5-yl)propyl)-2-(furan-2-...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]NECA from human adenosine A3 receptor expressed in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23FXPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Universit£ di Padova

Curated by ChEMBL
LigandPNGBDBM50064696(7-(3-(benzo[d][1,3]dioxol-5-yl)propyl)-2-(furan-2-...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [125I]-AB-MECA from human Adenosine A3 receptor expressed in HEK-293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2251H9KPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Universit£ di Padova

Curated by ChEMBL
LigandPNGBDBM50064696(7-(3-(benzo[d][1,3]dioxol-5-yl)propyl)-2-(furan-2-...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [125I]-AB-MECA from human Adenosine A3 receptor expressed in HEK-293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2251H9KPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Universit£ di Padova

Curated by ChEMBL
LigandPNGBDBM50064696(7-(3-(benzo[d][1,3]dioxol-5-yl)propyl)-2-(furan-2-...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibition of 1 uM NECA-stimulated cyclic AMP levels in human plateletsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2251H9KPubMed