null

SMILES: Nc1ncnc2n(cnc12)[C@H]1C[C@@H](OCC(=O)NO)C=C1

InChI Key: InChIKey=IDSNWXKWAHXXNG-SFYZADRCSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50119854   

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
Adenylate cyclase type 5 (Homo sapiens (Human))	BDBM50119854 (2-{[(1R,4S)-4-(6-amino-9H-purin-9-yl)cyclopent-2-e...) Show SMILES Nc1ncnc2n(cnc12)[C@H]1C[C@@H](OCC(=O)NO)C=C1 |c:21| Show InChI InChI=1S/C12H14N6O3/c13-11-10-12(15-5-14-11)18(6-16-10)7-1-2-8(3-7)21-4-9(19)17-20/h1-2,5-8,20H,3-4H2,(H,17,19)(H2,13,14,15)/t7-,8+/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.02E+5	n/a	n/a	n/a	n/a	n/a	n/a
Millennium Pharmaceuticals, Inc. Curated by ChEMBL					Assay Description Inhibitory concentration of the compound against Type V Adenyl Cyclase enzyme				Bioorg Med Chem Lett 12: 3089-92 (2002) BindingDB Entry DOI: 10.7270/Q2T43SFX
					More data for this Ligand-Target Pair
Adenylate cyclase type 5 (Homo sapiens (Human))	BDBM50119854 (2-{[(1R,4S)-4-(6-amino-9H-purin-9-yl)cyclopent-2-e...) Show SMILES Nc1ncnc2n(cnc12)[C@H]1C[C@@H](OCC(=O)NO)C=C1 |c:21| Show InChI InChI=1S/C12H14N6O3/c13-11-10-12(15-5-14-11)18(6-16-10)7-1-2-8(3-7)21-4-9(19)17-20/h1-2,5-8,20H,3-4H2,(H,17,19)(H2,13,14,15)/t7-,8+/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	9.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Millennium Pharmaceuticals, Inc. Curated by ChEMBL					Assay Description Inhibitory concentration of the compound against Type V Adenyl Cyclase enzyme				Bioorg Med Chem Lett 12: 3089-92 (2002) BindingDB Entry DOI: 10.7270/Q2T43SFX
					More data for this Ligand-Target Pair