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BDBM181010 US9133197, 1

SMILES: Cn1c(nc2c(N)nc(CCCCO)nc12)-n1nccn1

InChI Key: InChIKey=LXKQSSJIYWOEPP-UHFFFAOYSA-N

Data: 4 KI  1 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 = 181010   
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))
BDBM181010
PNG
(US9133197, 1)
Show SMILES Cn1c(nc2c(N)nc(CCCCO)nc12)-n1nccn1
Show InChI InChI=1S/C12H16N8O/c1-19-11-9(18-12(19)20-14-5-6-15-20)10(13)16-8(17-11)4-2-3-7-21/h5-6,21H,2-4,7H2,1H3,(H2,13,16,17)
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US Patent
51 -9.94n/an/an/an/an/a7.425



SIGMA-TAU INDUSTRIE FARMACEUTICHE RIUNITE S.P.A.

US Patent


Assay Description
Competition binding experiments have been performed incubating membranes from CHO-K1 cells stably transfected with the human adenosine A1 receptor (c...


US Patent US9133197 (2015)


BindingDB Entry DOI: 10.7270/Q2542MB7
More data for this
Ligand-Target Pair
Adenosine receptor A2a


(Homo sapiens (Human))
BDBM181010
PNG
(US9133197, 1)
Show SMILES Cn1c(nc2c(N)nc(CCCCO)nc12)-n1nccn1
Show InChI InChI=1S/C12H16N8O/c1-19-11-9(18-12(19)20-14-5-6-15-20)10(13)16-8(17-11)4-2-3-7-21/h5-6,21H,2-4,7H2,1H3,(H2,13,16,17)
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MMDB

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US Patent
53n/an/an/an/an/an/a7.4n/a



SIGMA-TAU INDUSTRIE FARMACEUTICHE RIUNITE S.P.A.

US Patent


Assay Description
The protein concentration of membrane suspension was determined using the Bradford method (Pierce, Rockford, Ill., USA) with bovine albumin as standa...


US Patent US9133197 (2015)


BindingDB Entry DOI: 10.7270/Q2542MB7
More data for this
Ligand-Target Pair
Adenosine receptor A2a


(Homo sapiens (Human))
BDBM181010
PNG
(US9133197, 1)
Show SMILES Cn1c(nc2c(N)nc(CCCCO)nc12)-n1nccn1
Show InChI InChI=1S/C12H16N8O/c1-19-11-9(18-12(19)20-14-5-6-15-20)10(13)16-8(17-11)4-2-3-7-21/h5-6,21H,2-4,7H2,1H3,(H2,13,16,17)
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Article
PubMed
53n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Urbino

Curated by ChEMBL


Assay Description
Displacement of [3H]ZM241385 from human recombinant adenosine A2A receptor expressed in HEK293 cells after 1 hr by competitive binding assay


J Med Chem 56: 5456-63 (2013)


Article DOI: 10.1021/jm400491x
BindingDB Entry DOI: 10.7270/Q2R49TQK
More data for this
Ligand-Target Pair
Adenosine receptor A1


(Homo sapiens (Human))
BDBM181010
PNG
(US9133197, 1)
Show SMILES Cn1c(nc2c(N)nc(CCCCO)nc12)-n1nccn1
Show InChI InChI=1S/C12H16N8O/c1-19-11-9(18-12(19)20-14-5-6-15-20)10(13)16-8(17-11)4-2-3-7-21/h5-6,21H,2-4,7H2,1H3,(H2,13,16,17)
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Article
PubMed
150n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Urbino

Curated by ChEMBL


Assay Description
Displacement of [3H]DPCPX from human recombinant adenosine A1 receptor expressed in CHO-K1 cells after 60 mins


J Med Chem 56: 5456-63 (2013)


Article DOI: 10.1021/jm400491x
BindingDB Entry DOI: 10.7270/Q2R49TQK
More data for this
Ligand-Target Pair
Adenosine receptor A2a


(Homo sapiens (Human))
BDBM181010
PNG
(US9133197, 1)
Show SMILES Cn1c(nc2c(N)nc(CCCCO)nc12)-n1nccn1
Show InChI InChI=1S/C12H16N8O/c1-19-11-9(18-12(19)20-14-5-6-15-20)10(13)16-8(17-11)4-2-3-7-21/h5-6,21H,2-4,7H2,1H3,(H2,13,16,17)
PDB
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NCI pathway
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KEGG

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Article
PubMed
n/an/a 2.10E+3n/an/an/an/an/an/a



Universit£ degli Studi di Urbino

Curated by ChEMBL


Assay Description
Antagonist activity at human adenosine A2A receptor expressed in HEK293 cells assessed as inhibition of NECA-induced cAMP accumulation incubated for ...


J Med Chem 56: 5456-63 (2013)


Article DOI: 10.1021/jm400491x
BindingDB Entry DOI: 10.7270/Q2R49TQK
More data for this
Ligand-Target Pair