Found 4 hits of ic50 for monomerid = 50199699 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
cAMP-specific 3',5'-cyclic phosphodiesterase 4B
(Homo sapiens (Human)) | BDBM50199699
(CHEMBL3986586)Show SMILES CCn1nc(cc(NC(=O)Nc2c(Cl)cncc2Cl)c1=O)-c1cccc(c1)-c1cccc(c1)C(=O)NCCN1CCOCC1 Show InChI InChI=1S/C31H31Cl2N7O4/c1-2-40-30(42)27(36-31(43)37-28-24(32)18-34-19-25(28)33)17-26(38-40)22-7-3-5-20(15-22)21-6-4-8-23(16-21)29(41)35-9-10-39-11-13-44-14-12-39/h3-8,15-19H,2,9-14H2,1H3,(H,35,41)(H2,34,36,37,43) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 0.0140 | n/a | n/a | n/a | n/a | n/a | n/a |
Rhône-Poulenc Rorer
Curated by ChEMBL
| Assay Description Inhibition of human recombinant PDE4B1 assessed as reduction in [3H]cAMP hydrolysis to [3H]AMP incubated for 60 mins by PDE-SPA assay |
J Med Chem 59: 10479-10497 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00829 BindingDB Entry DOI: 10.7270/Q21G0P75 |
More data for this Ligand-Target Pair | |
Adenosine receptor A1
(Homo sapiens (Human)) | BDBM50199699
(CHEMBL3986586)Show SMILES CCn1nc(cc(NC(=O)Nc2c(Cl)cncc2Cl)c1=O)-c1cccc(c1)-c1cccc(c1)C(=O)NCCN1CCOCC1 Show InChI InChI=1S/C31H31Cl2N7O4/c1-2-40-30(42)27(36-31(43)37-28-24(32)18-34-19-25(28)33)17-26(38-40)22-7-3-5-20(15-22)21-6-4-8-23(16-21)29(41)35-9-10-39-11-13-44-14-12-39/h3-8,15-19H,2,9-14H2,1H3,(H,35,41)(H2,34,36,37,43) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 15 | n/a | n/a | n/a | n/a | n/a | n/a |
Rhône-Poulenc Rorer
Curated by ChEMBL
| Assay Description Antagonist activity at adenosine A1 receptor (unknown origin) |
J Med Chem 59: 10479-10497 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00829 BindingDB Entry DOI: 10.7270/Q21G0P75 |
More data for this Ligand-Target Pair | |
Adenosine receptor A2a
(Homo sapiens (Human)) | BDBM50199699
(CHEMBL3986586)Show SMILES CCn1nc(cc(NC(=O)Nc2c(Cl)cncc2Cl)c1=O)-c1cccc(c1)-c1cccc(c1)C(=O)NCCN1CCOCC1 Show InChI InChI=1S/C31H31Cl2N7O4/c1-2-40-30(42)27(36-31(43)37-28-24(32)18-34-19-25(28)33)17-26(38-40)22-7-3-5-20(15-22)21-6-4-8-23(16-21)29(41)35-9-10-39-11-13-44-14-12-39/h3-8,15-19H,2,9-14H2,1H3,(H,35,41)(H2,34,36,37,43) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 33 | n/a | n/a | n/a | n/a | n/a | n/a |
Rhône-Poulenc Rorer
Curated by ChEMBL
| Assay Description Antagonist activity at adenosine A2a receptor (unknown origin) |
J Med Chem 59: 10479-10497 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00829 BindingDB Entry DOI: 10.7270/Q21G0P75 |
More data for this Ligand-Target Pair | |
Adenosine receptor A2b
(Homo sapiens (Human)) | BDBM50199699
(CHEMBL3986586)Show SMILES CCn1nc(cc(NC(=O)Nc2c(Cl)cncc2Cl)c1=O)-c1cccc(c1)-c1cccc(c1)C(=O)NCCN1CCOCC1 Show InChI InChI=1S/C31H31Cl2N7O4/c1-2-40-30(42)27(36-31(43)37-28-24(32)18-34-19-25(28)33)17-26(38-40)22-7-3-5-20(15-22)21-6-4-8-23(16-21)29(41)35-9-10-39-11-13-44-14-12-39/h3-8,15-19H,2,9-14H2,1H3,(H,35,41)(H2,34,36,37,43) | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 145 | n/a | n/a | n/a | n/a | n/a | n/a |
Rhône-Poulenc Rorer
Curated by ChEMBL
| Assay Description Antagonist activity at adenosine A2b receptor (unknown origin) |
J Med Chem 59: 10479-10497 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00829 BindingDB Entry DOI: 10.7270/Q21G0P75 |
More data for this Ligand-Target Pair | |