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SMILES: O=C(Nc1cnc(-c2ccncc2)c(n1)-c1cnco1)C1CC1

InChI Key: InChIKey=WIPKZBPVDCSZIB-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50336993   

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))	BDBM50336993 (CHEMBL1672625 | N-[6-(1,3-Oxazol-5-yl)-5-pyridin-4...) Show SMILES O=C(Nc1cnc(-c2ccncc2)c(n1)-c1cnco1)C1CC1 Show InChI InChI=1S/C16H13N5O2/c22-16(11-1-2-11)21-13-8-19-14(10-3-5-17-6-4-10)15(20-13)12-7-18-9-23-12/h3-9,11H,1-2H2,(H,20,21,22)	NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	43	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 A2a (Homo sapiens (Human))	BDBM50336993 (CHEMBL1672625 | N-[6-(1,3-Oxazol-5-yl)-5-pyridin-4...) Show SMILES O=C(Nc1cnc(-c2ccncc2)c(n1)-c1cnco1)C1CC1 Show InChI InChI=1S/C16H13N5O2/c22-16(11-1-2-11)21-13-8-19-14(10-3-5-17-6-4-10)15(20-13)12-7-18-9-23-12/h3-9,11H,1-2H2,(H,20,21,22)	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	634	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