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SMILES: CCC(=O)Nc1cnc(-c2ccncc2)c(n1)-c1ccco1

InChI Key: InChIKey=JHBSNTNTZSANRS-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50336983   

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 A2b (Homo sapiens (Human))	BDBM50336983 (CHEMBL1672613 | N-[6-(2-Furyl)-5-pyridin-4-ylpyraz...) Show SMILES CCC(=O)Nc1cnc(-c2ccncc2)c(n1)-c1ccco1 Show InChI InChI=1S/C16H14N4O2/c1-2-14(21)19-13-10-18-15(11-5-7-17-8-6-11)16(20-13)12-4-3-9-22-12/h3-10H,2H2,1H3,(H,19,20,21)	NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	3.5	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 adenosine A2B receptor expressed in HEK293 cells after 60 mins by filtration binding assay				ACS Med Chem Lett 2: 213-218 (2011) Article DOI: 10.1021/ml100249e BindingDB Entry DOI: 10.7270/Q2PG1S10
					More data for this Ligand-Target Pair
Adenosine receptor A1 (Homo sapiens (Human))	BDBM50336983 (CHEMBL1672613 | N-[6-(2-Furyl)-5-pyridin-4-ylpyraz...) Show SMILES CCC(=O)Nc1cnc(-c2ccncc2)c(n1)-c1ccco1 Show InChI InChI=1S/C16H14N4O2/c1-2-14(21)19-13-10-18-15(11-5-7-17-8-6-11)16(20-13)12-4-3-9-22-12/h3-10H,2H2,1H3,(H,19,20,21)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	42	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 adenosine A1 receptor expressed in CHO cells after 90 mins by filtration binding assay				ACS Med Chem Lett 2: 213-218 (2011) Article DOI: 10.1021/ml100249e BindingDB Entry DOI: 10.7270/Q2PG1S10
					More data for this Ligand-Target Pair
Adenosine receptor A2a (Homo sapiens (Human))	BDBM50336983 (CHEMBL1672613 | N-[6-(2-Furyl)-5-pyridin-4-ylpyraz...) Show SMILES CCC(=O)Nc1cnc(-c2ccncc2)c(n1)-c1ccco1 Show InChI InChI=1S/C16H14N4O2/c1-2-14(21)19-13-10-18-15(11-5-7-17-8-6-11)16(20-13)12-4-3-9-22-12/h3-10H,2H2,1H3,(H,19,20,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	55	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]ZM241385 from human adenosine A2A receptor expressed in HeLa cells after 60 mins by scintillation proximity assay				ACS Med Chem Lett 2: 213-218 (2011) Article DOI: 10.1021/ml100249e BindingDB Entry DOI: 10.7270/Q2PG1S10
					More data for this Ligand-Target Pair
Adenosine receptor A3 (Homo sapiens (Human))	BDBM50336983 (CHEMBL1672613 | N-[6-(2-Furyl)-5-pyridin-4-ylpyraz...) Show SMILES CCC(=O)Nc1cnc(-c2ccncc2)c(n1)-c1ccco1 Show InChI InChI=1S/C16H14N4O2/c1-2-14(21)19-13-10-18-15(11-5-7-17-8-6-11)16(20-13)12-4-3-9-22-12/h3-10H,2H2,1H3,(H,19,20,21)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	373	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]NECA from human adenosine A3 receptor expressed in HeLa cells after 3 hrs by filtration binding assay				ACS Med Chem Lett 2: 213-218 (2011) Article DOI: 10.1021/ml100249e BindingDB Entry DOI: 10.7270/Q2PG1S10
					More data for this Ligand-Target Pair