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SMILES: Cc1nc(CO)c(o1)-c1c(nc(N)c2nn(Cc3ccccn3)nc12)-c1cccc(c1)C#N

InChI Key:

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 561405   

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))	BDBM561405 (3-(4-amino-7-(4-(hydroxymethyl)-2-methyloxazol-5-y...) Show SMILES Cc1nc(CO)c(o1)-c1c(nc(N)c2nn(Cc3ccccn3)nc12)-c1cccc(c1)C#N |(-1.84,4.89,;-.93,3.64,;.61,3.64,;1.09,2.18,;2.55,1.7,;3.64,2.79,;-.16,1.27,;-1.41,2.18,;-.16,-.27,;-1.49,-1.04,;-1.49,-2.58,;-.16,-3.35,;-.16,-4.89,;1.17,-2.58,;2.64,-3.05,;3.54,-1.81,;5.08,-1.81,;5.85,-.47,;5.08,.86,;5.85,2.19,;7.39,2.19,;8.16,.86,;7.39,-.47,;2.64,-.56,;1.17,-1.04,;-2.83,-.27,;-2.83,1.27,;-4.16,2.04,;-5.5,1.27,;-5.5,-.27,;-4.16,-1.04,;-6.83,-1.04,;-8.16,-1.81,)| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		<10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Adenosine receptor A2b (Homo sapiens (Human))	BDBM561405 (3-(4-amino-7-(4-(hydroxymethyl)-2-methyloxazol-5-y...) Show SMILES Cc1nc(CO)c(o1)-c1c(nc(N)c2nn(Cc3ccccn3)nc12)-c1cccc(c1)C#N |(-1.84,4.89,;-.93,3.64,;.61,3.64,;1.09,2.18,;2.55,1.7,;3.64,2.79,;-.16,1.27,;-1.41,2.18,;-.16,-.27,;-1.49,-1.04,;-1.49,-2.58,;-.16,-3.35,;-.16,-4.89,;1.17,-2.58,;2.64,-3.05,;3.54,-1.81,;5.08,-1.81,;5.85,-.47,;5.08,.86,;5.85,2.19,;7.39,2.19,;8.16,.86,;7.39,-.47,;2.64,-.56,;1.17,-1.04,;-2.83,-.27,;-2.83,1.27,;-4.16,2.04,;-5.5,1.27,;-5.5,-.27,;-4.16,-1.04,;-6.83,-1.04,;-8.16,-1.81,)| Show InChI	NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	n/a	n/a	<10	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair