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BDBM50003267 6-guanidino- NECA::CHEMBL405144

SMILES: CCNC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NC(N)=N)ncnc12

InChI Key: InChIKey=UICFBMWXKSHXKU-WOUKDFQISA-N

Data: 1 EC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50003267   
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 A2b


(Homo sapiens (Human))
BDBM50003267
PNG
(6-guanidino- NECA | CHEMBL405144)
Show SMILES CCNC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NC(N)=N)ncnc12
Show InChI InChI=1S/C13H20N8O3/c1-2-16-3-6-8(22)9(23)12(24-6)21-5-19-7-10(20-13(14)15)17-4-18-11(7)21/h4-6,8-9,12,16,22-23H,2-3H2,1H3,(H4,14,15,17,18,20)/t6-,8-,9-,12-/m1/s1
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.84E+7n/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