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BDBM50389893 CHEMBL2071047

SMILES: Cn1cc2c(n1)nc(NC(=O)NC1CCN(CC1)C(=O)NCc1ccc(Cl)cc1)n1nc(nc21)-c1ccco1

InChI Key: InChIKey=VZKWWDWVHHXLRU-UHFFFAOYSA-N

Data: 3 KI  2 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50389893   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Adenosine receptor A3


(Homo sapiens (Human))
BDBM50389893
PNG
(CHEMBL2071047)
Show SMILES Cn1cc2c(n1)nc(NC(=O)NC1CCN(CC1)C(=O)NCc1ccc(Cl)cc1)n1nc(nc21)-c1ccco1
Show InChI InChI=1S/C25H25ClN10O3/c1-34-14-18-20(32-34)30-23(36-22(18)29-21(33-36)19-3-2-12-39-19)31-24(37)28-17-8-10-35(11-9-17)25(38)27-13-15-4-6-16(26)7-5-15/h2-7,12,14,17H,8-11,13H2,1H3,(H,27,38)(H2,28,30,31,32,37)
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25n/an/an/an/an/an/an/an/a



Universit£ di Ferrara

Curated by ChEMBL


Assay Description
Displacement of [3H]MRE-3008-F20 from human adenosine A3 receptor expressed in CHO cells after 120 mins by scintillation counter


J Med Chem 55: 5380-90 (2012)


Article DOI: 10.1021/jm300323t
BindingDB Entry DOI: 10.7270/Q2CN7509
More data for this
Ligand-Target Pair
Adenosine receptor A1


(Homo sapiens (Human))
BDBM50389893
PNG
(CHEMBL2071047)
Show SMILES Cn1cc2c(n1)nc(NC(=O)NC1CCN(CC1)C(=O)NCc1ccc(Cl)cc1)n1nc(nc21)-c1ccco1
Show InChI InChI=1S/C25H25ClN10O3/c1-34-14-18-20(32-34)30-23(36-22(18)29-21(33-36)19-3-2-12-39-19)31-24(37)28-17-8-10-35(11-9-17)25(38)27-13-15-4-6-16(26)7-5-15/h2-7,12,14,17H,8-11,13H2,1H3,(H,27,38)(H2,28,30,31,32,37)
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614n/an/an/an/an/an/an/an/a



Universit£ di Ferrara

Curated by ChEMBL


Assay Description
Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cells after 120 mins by scintillation counter


J Med Chem 55: 5380-90 (2012)


Article DOI: 10.1021/jm300323t
BindingDB Entry DOI: 10.7270/Q2CN7509
More data for this
Ligand-Target Pair
Adenosine receptor A2a


(Homo sapiens (Human))
BDBM50389893
PNG
(CHEMBL2071047)
Show SMILES Cn1cc2c(n1)nc(NC(=O)NC1CCN(CC1)C(=O)NCc1ccc(Cl)cc1)n1nc(nc21)-c1ccco1
Show InChI InChI=1S/C25H25ClN10O3/c1-34-14-18-20(32-34)30-23(36-22(18)29-21(33-36)19-3-2-12-39-19)31-24(37)28-17-8-10-35(11-9-17)25(38)27-13-15-4-6-16(26)7-5-15/h2-7,12,14,17H,8-11,13H2,1H3,(H,27,38)(H2,28,30,31,32,37)
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1.14E+3n/an/an/an/an/an/an/an/a



Universit£ di Ferrara

Curated by ChEMBL


Assay Description
Displacement of [3H]ZM241385 from human adenosine A2A receptor expressed in CHO cells after 60 mins by scintillation counter


J Med Chem 55: 5380-90 (2012)


Article DOI: 10.1021/jm300323t
BindingDB Entry DOI: 10.7270/Q2CN7509
More data for this
Ligand-Target Pair
Adenosine receptor A2b


(Homo sapiens (Human))
BDBM50389893
PNG
(CHEMBL2071047)
Show SMILES Cn1cc2c(n1)nc(NC(=O)NC1CCN(CC1)C(=O)NCc1ccc(Cl)cc1)n1nc(nc21)-c1ccco1
Show InChI InChI=1S/C25H25ClN10O3/c1-34-14-18-20(32-34)30-23(36-22(18)29-21(33-36)19-3-2-12-39-19)31-24(37)28-17-8-10-35(11-9-17)25(38)27-13-15-4-6-16(26)7-5-15/h2-7,12,14,17H,8-11,13H2,1H3,(H,27,38)(H2,28,30,31,32,37)
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n/an/a 505n/an/an/an/an/an/a



Universit£ di Ferrara

Curated by ChEMBL


Assay Description
Antagonist activity at human adenosine A2B receptor expressed in CHO cells assessed as inhibition of NECA-induced cAMP production


J Med Chem 55: 5380-90 (2012)


Article DOI: 10.1021/jm300323t
BindingDB Entry DOI: 10.7270/Q2CN7509
More data for this
Ligand-Target Pair
Adenosine receptor A3


(Homo sapiens (Human))
BDBM50389893
PNG
(CHEMBL2071047)
Show SMILES Cn1cc2c(n1)nc(NC(=O)NC1CCN(CC1)C(=O)NCc1ccc(Cl)cc1)n1nc(nc21)-c1ccco1
Show InChI InChI=1S/C25H25ClN10O3/c1-34-14-18-20(32-34)30-23(36-22(18)29-21(33-36)19-3-2-12-39-19)31-24(37)28-17-8-10-35(11-9-17)25(38)27-13-15-4-6-16(26)7-5-15/h2-7,12,14,17H,8-11,13H2,1H3,(H,27,38)(H2,28,30,31,32,37)
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n/an/a 90n/an/an/an/an/an/a



Universit£ di Ferrara

Curated by ChEMBL


Assay Description
Antagonist activity at human adenosine A3 receptor expressed in CHO cells assessed as forskolin/C1-IB-MECA-induced inhibition of cAMP production


J Med Chem 55: 5380-90 (2012)


Article DOI: 10.1021/jm300323t
BindingDB Entry DOI: 10.7270/Q2CN7509
More data for this
Ligand-Target Pair