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BDBM50376932 CHEMBL410104

SMILES: NNc1nc(OCCc2c[nH]c3cc(Br)ccc23)nc2n(cnc12)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

InChI Key: InChIKey=GMXUEMZFNYPWFA-NVQRDWNXSA-N

Data: 2 KI  2 EC50

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 4 hits for monomerid = 50376932   
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 A1


(Homo sapiens (Human))
BDBM50376932
PNG
(CHEMBL410104)
Show SMILES NNc1nc(OCCc2c[nH]c3cc(Br)ccc23)nc2n(cnc12)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C20H22BrN7O5/c21-10-1-2-11-9(6-23-12(11)5-10)3-4-32-20-25-17(27-22)14-18(26-20)28(8-24-14)19-16(31)15(30)13(7-29)33-19/h1-2,5-6,8,13,15-16,19,23,29-31H,3-4,7,22H2,(H,25,26,27)/t13-,15-,16-,19-/m1/s1
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Article
PubMed
350n/an/an/an/an/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL


Assay Description
Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cells


J Med Chem 51: 2088-99 (2008)


Article DOI: 10.1021/jm701442d
BindingDB Entry DOI: 10.7270/Q2R49RNV
More data for this
Ligand-Target Pair
Adenosine receptor A2a


(Homo sapiens (Human))
BDBM50376932
PNG
(CHEMBL410104)
Show SMILES NNc1nc(OCCc2c[nH]c3cc(Br)ccc23)nc2n(cnc12)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C20H22BrN7O5/c21-10-1-2-11-9(6-23-12(11)5-10)3-4-32-20-25-17(27-22)14-18(26-20)28(8-24-14)19-16(31)15(30)13(7-29)33-19/h1-2,5-6,8,13,15-16,19,23,29-31H,3-4,7,22H2,(H,25,26,27)/t13-,15-,16-,19-/m1/s1
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2.05E+3n/an/an/an/an/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL


Assay Description
Displacement of [3H]CGS-21680 from human adenosine A2A receptor expressed in HEK293 cells


J Med Chem 51: 2088-99 (2008)


Article DOI: 10.1021/jm701442d
BindingDB Entry DOI: 10.7270/Q2R49RNV
More data for this
Ligand-Target Pair
Adenosine receptor A2b


(Homo sapiens (Human))
BDBM50376932
PNG
(CHEMBL410104)
Show SMILES NNc1nc(OCCc2c[nH]c3cc(Br)ccc23)nc2n(cnc12)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C20H22BrN7O5/c21-10-1-2-11-9(6-23-12(11)5-10)3-4-32-20-25-17(27-22)14-18(26-20)28(8-24-14)19-16(31)15(30)13(7-29)33-19/h1-2,5-6,8,13,15-16,19,23,29-31H,3-4,7,22H2,(H,25,26,27)/t13-,15-,16-,19-/m1/s1
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PubMed
n/an/an/an/a 174n/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL


Assay Description
Agonist activity at human adenosine A2B receptor expressed in CHO cells assessed as stimulation of adenylate cyclase


J Med Chem 51: 2088-99 (2008)


Article DOI: 10.1021/jm701442d
BindingDB Entry DOI: 10.7270/Q2R49RNV
More data for this
Ligand-Target Pair
Adenosine receptor A2b


(Homo sapiens (Human))
BDBM50376932
PNG
(CHEMBL410104)
Show SMILES NNc1nc(OCCc2c[nH]c3cc(Br)ccc23)nc2n(cnc12)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C20H22BrN7O5/c21-10-1-2-11-9(6-23-12(11)5-10)3-4-32-20-25-17(27-22)14-18(26-20)28(8-24-14)19-16(31)15(30)13(7-29)33-19/h1-2,5-6,8,13,15-16,19,23,29-31H,3-4,7,22H2,(H,25,26,27)/t13-,15-,16-,19-/m1/s1
NCI pathway
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PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 174n/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL


Assay Description
Agonist activity at human adenosine A2B receptor expressed in CHO cells assessed as stimulation of adenylate cyclase


J Med Chem 51: 2088-99 (2008)


Article DOI: 10.1021/jm701442d
BindingDB Entry DOI: 10.7270/Q2R49RNV
More data for this
Ligand-Target Pair