BDBM22926 3-(6-amino-9H-purin-9-yl)nonan-2-ol::EHNA::Erythro-9-(2-hydroxy-3-nonyl)adenine
SMILES CCCCCCC(C(C)O)n1cnc2c(N)ncnc12
InChI Key InChIKey=IOSAAWHGJUZBOG-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 6 hits for monomerid = 22926
Affinity DataKi: 37nM ΔG°: -10.0kcal/molepH: 7.4 T: 2°CAssay Description:The reaction velocity was measured by change in absorbance at 265nm (A265) resulting from the deamination of adenosine. The reaction was started by a...More data for this Ligand-Target Pair
TargetAdenosine receptor A1(Rattus norvegicus (rat))
National Institute Of Diabetes, Digestive And Kidney Diseases
Curated by PDSP Ki Database
National Institute Of Diabetes, Digestive And Kidney Diseases
Curated by PDSP Ki Database
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
National Institute Of Diabetes, Digestive And Kidney Diseases
Curated by PDSP Ki Database
National Institute Of Diabetes, Digestive And Kidney Diseases
Curated by PDSP Ki Database
TargetTransmembrane and immunoglobulin domain-containing 3(RAT)
National Institute Of Diabetes, Digestive And Kidney Diseases
Curated by PDSP Ki Database
National Institute Of Diabetes, Digestive And Kidney Diseases
Curated by PDSP Ki Database
Affinity DataIC50: >1.00E+5nMpH: 7.5 T: 2°CAssay Description:Enzymatic activities were assayed using [3H] cAMP and [3H]cGMP as substrate.More data for this Ligand-Target Pair
TargetcGMP-dependent 3',5'-cyclic phosphodiesterase(Homo sapiens (Human))
University Of North Carolina
University Of North Carolina
Affinity DataIC50: 800nMpH: 7.5 T: 2°CAssay Description:Enzymatic activities were assayed using [3H] cAMP and [3H]cGMP as substrate.More data for this Ligand-Target Pair