null

SMILES: OC[C@@]12C[C@@H]1[C@H]([C@H](O)[C@@H]2O)n1cnc2c(NC3CCCC3)ncnc12

InChI Key: InChIKey=PSTJTJSXZYZTNV-ZLQDYUCGSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 50088424   

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 A1 (Rattus norvegicus (rat))	BDBM50088424 ((1R,2R,3S,4R,5S)-4-(6-Cyclopentylamino-purin-9-yl)...) Show SMILES OC[C@@]12C[C@@H]1[C@H]([C@H](O)[C@@H]2O)n1cnc2c(NC3CCCC3)ncnc12 Show InChI InChI=1S/C17H23N5O3/c23-6-17-5-10(17)12(13(24)14(17)25)22-8-20-11-15(18-7-19-16(11)22)21-9-3-1-2-4-9/h7-10,12-14,23-25H,1-6H2,(H,18,19,21)/t10-,12-,13+,14+,17+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	5.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Displacement of [3H]R-PIA from rat brain membrane Adenosine A1 receptor				J Med Chem 43: 2196-203 (2000) BindingDB Entry DOI: 10.7270/Q2ZW1MM5
					More data for this Ligand-Target Pair
Adenosine receptor A1 (Rattus norvegicus (rat))	BDBM50088424 ((1R,2R,3S,4R,5S)-4-(6-Cyclopentylamino-purin-9-yl)...) Show SMILES OC[C@@]12C[C@@H]1[C@H]([C@H](O)[C@@H]2O)n1cnc2c(NC3CCCC3)ncnc12 Show InChI InChI=1S/C17H23N5O3/c23-6-17-5-10(17)12(13(24)14(17)25)22-8-20-11-15(18-7-19-16(11)22)21-9-3-1-2-4-9/h7-10,12-14,23-25H,1-6H2,(H,18,19,21)/t10-,12-,13+,14+,17+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	5.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
NIDDK Curated by ChEMBL					Assay Description Ability to displace specific radioligand [3H]R-PIA binding at Adenosine A1 receptor in rat brain membrane				Bioorg Med Chem Lett 11: 1333-7 (2001) BindingDB Entry DOI: 10.7270/Q2445N1F
					More data for this Ligand-Target Pair
Adenosine receptor A3 (Homo sapiens (Human))	BDBM50088424 ((1R,2R,3S,4R,5S)-4-(6-Cyclopentylamino-purin-9-yl)...) Show SMILES OC[C@@]12C[C@@H]1[C@H]([C@H](O)[C@@H]2O)n1cnc2c(NC3CCCC3)ncnc12 Show InChI InChI=1S/C17H23N5O3/c23-6-17-5-10(17)12(13(24)14(17)25)22-8-20-11-15(18-7-19-16(11)22)21-9-3-1-2-4-9/h7-10,12-14,23-25H,1-6H2,(H,18,19,21)/t10-,12-,13+,14+,17+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	170	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
NIDDK Curated by ChEMBL					Assay Description Ability to displace specific radioligand [125I]AB-MECA binding at human Adenosine A3 receptor expressed in CHO cells				Bioorg Med Chem Lett 11: 1333-7 (2001) BindingDB Entry DOI: 10.7270/Q2445N1F
					More data for this Ligand-Target Pair
Adenosine receptor A3 (Homo sapiens (Human))	BDBM50088424 ((1R,2R,3S,4R,5S)-4-(6-Cyclopentylamino-purin-9-yl)...) Show SMILES OC[C@@]12C[C@@H]1[C@H]([C@H](O)[C@@H]2O)n1cnc2c(NC3CCCC3)ncnc12 Show InChI InChI=1S/C17H23N5O3/c23-6-17-5-10(17)12(13(24)14(17)25)22-8-20-11-15(18-7-19-16(11)22)21-9-3-1-2-4-9/h7-10,12-14,23-25H,1-6H2,(H,18,19,21)/t10-,12-,13+,14+,17+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	170	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Displacement of [125I]- AB-MECA from human adenosine A3 receptor expressed in HEK cells				J Med Chem 43: 2196-203 (2000) BindingDB Entry DOI: 10.7270/Q2ZW1MM5
					More data for this Ligand-Target Pair
Adenosine receptor A2a (Rattus norvegicus (rat))	BDBM50088424 ((1R,2R,3S,4R,5S)-4-(6-Cyclopentylamino-purin-9-yl)...) Show SMILES OC[C@@]12C[C@@H]1[C@H]([C@H](O)[C@@H]2O)n1cnc2c(NC3CCCC3)ncnc12 Show InChI InChI=1S/C17H23N5O3/c23-6-17-5-10(17)12(13(24)14(17)25)22-8-20-11-15(18-7-19-16(11)22)21-9-3-1-2-4-9/h7-10,12-14,23-25H,1-6H2,(H,18,19,21)/t10-,12-,13+,14+,17+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	6.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
NIDDK Curated by ChEMBL					Assay Description Ability to displace specific radioligand [3H]-CGS- 21680 binding at A2A receptors (rA2A) in rat brain membrane				Bioorg Med Chem Lett 11: 1333-7 (2001) BindingDB Entry DOI: 10.7270/Q2445N1F
					More data for this Ligand-Target Pair
Adenosine receptor A2a (Rattus norvegicus (rat))	BDBM50088424 ((1R,2R,3S,4R,5S)-4-(6-Cyclopentylamino-purin-9-yl)...) Show SMILES OC[C@@]12C[C@@H]1[C@H]([C@H](O)[C@@H]2O)n1cnc2c(NC3CCCC3)ncnc12 Show InChI InChI=1S/C17H23N5O3/c23-6-17-5-10(17)12(13(24)14(17)25)22-8-20-11-15(18-7-19-16(11)22)21-9-3-1-2-4-9/h7-10,12-14,23-25H,1-6H2,(H,18,19,21)/t10-,12-,13+,14+,17+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	6.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Displacement of specific [3H]-CGS- 21680 binding to adenosine A2A receptor in rat striatal membranes				J Med Chem 43: 2196-203 (2000) BindingDB Entry DOI: 10.7270/Q2ZW1MM5
					More data for this Ligand-Target Pair
Adenosine receptor A2b (Homo sapiens (Human))	BDBM50088424 ((1R,2R,3S,4R,5S)-4-(6-Cyclopentylamino-purin-9-yl)...) Show SMILES OC[C@@]12C[C@@H]1[C@H]([C@H](O)[C@@H]2O)n1cnc2c(NC3CCCC3)ncnc12 Show InChI InChI=1S/C17H23N5O3/c23-6-17-5-10(17)12(13(24)14(17)25)22-8-20-11-15(18-7-19-16(11)22)21-9-3-1-2-4-9/h7-10,12-14,23-25H,1-6H2,(H,18,19,21)/t10-,12-,13+,14+,17+/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.39E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Displacement of [3H]- ZM-241385 from human adenosine A2B receptor expressed in HEK cells				J Med Chem 43: 2196-203 (2000) BindingDB Entry DOI: 10.7270/Q2ZW1MM5
					More data for this Ligand-Target Pair
Adenosine receptor A1 (Rattus norvegicus (rat))	BDBM50088424 ((1R,2R,3S,4R,5S)-4-(6-Cyclopentylamino-purin-9-yl)...) Show SMILES OC[C@@]12C[C@@H]1[C@H]([C@H](O)[C@@H]2O)n1cnc2c(NC3CCCC3)ncnc12 Show InChI InChI=1S/C17H23N5O3/c23-6-17-5-10(17)12(13(24)14(17)25)22-8-20-11-15(18-7-19-16(11)22)21-9-3-1-2-4-9/h7-10,12-14,23-25H,1-6H2,(H,18,19,21)/t10-,12-,13+,14+,17+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	100	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Stimulation of [35S]GTP-gamma-S, binding to adenosine A1 receptor of rat cerebral cortical membrane				J Med Chem 43: 2196-203 (2000) BindingDB Entry DOI: 10.7270/Q2ZW1MM5
					More data for this Ligand-Target Pair
Adenosine receptor A3 (Homo sapiens (Human))	BDBM50088424 ((1R,2R,3S,4R,5S)-4-(6-Cyclopentylamino-purin-9-yl)...) Show SMILES OC[C@@]12C[C@@H]1[C@H]([C@H](O)[C@@H]2O)n1cnc2c(NC3CCCC3)ncnc12 Show InChI InChI=1S/C17H23N5O3/c23-6-17-5-10(17)12(13(24)14(17)25)22-8-20-11-15(18-7-19-16(11)22)21-9-3-1-2-4-9/h7-10,12-14,23-25H,1-6H2,(H,18,19,21)/t10-,12-,13+,14+,17+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Stimulation of [35S]GTP-gamma-S, against human adenosine A3 receptor				J Med Chem 43: 2196-203 (2000) BindingDB Entry DOI: 10.7270/Q2ZW1MM5
					More data for this Ligand-Target Pair
Adenosine receptor A1 (Homo sapiens (Human))	BDBM50088424 ((1R,2R,3S,4R,5S)-4-(6-Cyclopentylamino-purin-9-yl)...) Show SMILES OC[C@@]12C[C@@H]1[C@H]([C@H](O)[C@@H]2O)n1cnc2c(NC3CCCC3)ncnc12 Show InChI InChI=1S/C17H23N5O3/c23-6-17-5-10(17)12(13(24)14(17)25)22-8-20-11-15(18-7-19-16(11)22)21-9-3-1-2-4-9/h7-10,12-14,23-25H,1-6H2,(H,18,19,21)/t10-,12-,13+,14+,17+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	22	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Stimulation of [35S]GTP-gamma-S, binding to human adenosine A1 receptor				J Med Chem 43: 2196-203 (2000) BindingDB Entry DOI: 10.7270/Q2ZW1MM5
					More data for this Ligand-Target Pair