BDBM50050617 6-(5-Amino-2-propoxy-phenyl)-1-ethyl-3-methyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one::CHEMBL439923
SMILES: CCCOc1ccc(N)cc1-c1nc2n(CC)nc(C)c2c(=O)[nH]1
InChI Key: InChIKey=BVZYXQOYVZEIIL-UHFFFAOYSA-N
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Phosphodiesterase 5A (Rattus norvegicus) | BDBM50050617 (6-(5-Amino-2-propoxy-phenyl)-1-ethyl-3-methyl-1,5-...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | n/a | n/a | 20 | n/a | n/a | n/a | n/a |
Laboratories Glaxo Wellcome Centre de Recherches Curated by ChEMBL | Assay Description Compound was tested for inhibition of stimulation of rat aortic smooth muscle cells (RSMC) | J Med Chem 39: 1635-44 (1996) Article DOI: 10.1021/jm950812j BindingDB Entry DOI: 10.7270/Q2057F1T | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
cGMP-specific 3',5'-cyclic phosphodiesterase (Homo sapiens (Human)) | BDBM50050617 (6-(5-Amino-2-propoxy-phenyl)-1-ethyl-3-methyl-1,5-...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 7 | n/a | n/a | n/a | n/a | n/a | n/a |
Laboratories Glaxo Wellcome Centre de Recherches Curated by ChEMBL | Assay Description Inhibition of Phosphodiesterase 5 from human | J Med Chem 39: 1635-44 (1996) Article DOI: 10.1021/jm950812j BindingDB Entry DOI: 10.7270/Q2057F1T | |||||||||||
More data for this Ligand-Target Pair |