BDBM50392808 CHEMBL2151255

SMILES: CC[C@@H](Oc1ccccc1)C(=O)Nc1nnc([nH]1)-c1ccccc1

InChI Key: InChIKey=HLRYLSLKGMHUIW-OAHLLOKOSA-N

Data: 3 KI

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 3 hits for monomerid = 50392808   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Adenosine receptor A2a (Homo sapiens (Human))	BDBM50392808 (CHEMBL2151255) Show SMILES CC[C@@H](Oc1ccccc1)C(=O)Nc1nnc([nH]1)-c1ccccc1 |r| Show InChI InChI=1S/C18H18N4O2/c1-2-15(24-14-11-7-4-8-12-14)17(23)20-18-19-16(21-22-18)13-9-5-3-6-10-13/h3-12,15H,2H2,1H3,(H2,19,20,21,22,23)/t15-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Displacement of [3H]CGS21680 from human A2A adenosine receptor expressed in HEK293 cells after 60 mins by liquid scintillation counting				ACS Med Chem Lett 3: 715-720 (2012) Article DOI: 10.1021/ml300097g BindingDB Entry DOI: 10.7270/Q27082HC
					More data for this Ligand-Target Pair
Adenosine receptor A1 (Homo sapiens (Human))	BDBM50392808 (CHEMBL2151255) Show SMILES CC[C@@H](Oc1ccccc1)C(=O)Nc1nnc([nH]1)-c1ccccc1 |r| Show InChI InChI=1S/C18H18N4O2/c1-2-15(24-14-11-7-4-8-12-14)17(23)20-18-19-16(21-22-18)13-9-5-3-6-10-13/h3-12,15H,2H2,1H3,(H2,19,20,21,22,23)/t15-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.50E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human A1 adenosine receptor expressed in CHO cells after 60 mins by liquid scintillation counting				ACS Med Chem Lett 3: 715-720 (2012) Article DOI: 10.1021/ml300097g BindingDB Entry DOI: 10.7270/Q27082HC
					More data for this Ligand-Target Pair
Adenosine receptor A3 (Homo sapiens (Human))	BDBM50392808 (CHEMBL2151255) Show SMILES CC[C@@H](Oc1ccccc1)C(=O)Nc1nnc([nH]1)-c1ccccc1 |r| Show InChI InChI=1S/C18H18N4O2/c1-2-15(24-14-11-7-4-8-12-14)17(23)20-18-19-16(21-22-18)13-9-5-3-6-10-13/h3-12,15H,2H2,1H3,(H2,19,20,21,22,23)/t15-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Displacement of [3H]DPCPX from human A3 adenosine receptor expressed in CHO cells after 60 mins by liquid scintillation counting				ACS Med Chem Lett 3: 715-720 (2012) Article DOI: 10.1021/ml300097g BindingDB Entry DOI: 10.7270/Q27082HC
					More data for this Ligand-Target Pair