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SMILES CC(C)CCn1cc2c(n1)nc(N)n1nc(nc21)-c1ccco1

InChI Key InChIKey=NXSARBYAOXIQJA-UHFFFAOYSA-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 14 hits for monomerid = 50094688   

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

Curated by ChEMBL
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  0.780nMAssay 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
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  0.780nMAssay Description:Displacement of [3H]-SCH- 58261 from human adenosine A2A receptor expressed in CHO cells; range 0.60-1.00More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WWTPubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Università degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  1.90nMAssay Description:Inhibition of [3H]-CGS- 21680 binding to Adenosine A2A receptor in rat striatal homogenates.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP23H4PubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Università degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  1.90nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81D1P
TargetAdenosine receptor A1(Homo sapiens (Human))
Università degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  2nMAssay Description:Displacement of [3H]-DPCPX from human adenosine A1 receptor expressed in CHO cells; range 1.72-2.36More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WWTPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Università degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  5.60nMAssay Description:Inhibition of [3H]-CHA binding to Adenosine A1 receptor in rat whole brain homogenates.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP23H4PubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Università degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  5.60nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81D1P
TargetAdenosine receptor A2b(Homo sapiens (Human))
Università degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  9.10nMAssay Description:Displacement of [3H]-DPCPX from Adenosine A2b receptor expressed in CHO cells; range 7.4-11.3More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WWTPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))TBA
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  700nMAssay Description:Binding affinity to human adenosine A3 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z18GV
TargetAdenosine receptor A3(Homo sapiens (Human))TBA
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  700nMAssay Description:Displacement of [3H]-MRE3008-F20 from human adenosine A3 receptor expressed in CHO cells; range 664-738More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WWTPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))TBA
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  700nMAssay 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))TBA
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  700nMAssay Description:Antagonist activity at human adenosine A3 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5P5ZPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))TBA
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  700nMAssay Description:Binding affinity for human adenosine A3 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2183609PubMed
TargetAdenosine receptor A3(Homo sapiens (Human))TBA
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)copy SMILEScopy InChI
Affinity DataKi:  7.08E+5nMAssay Description:Displacement of [3H]MRE3008-F20 from human adenosine A3 receptor expressed in CHO cells after 120 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP766QPubMed