Found 6 hits for monomerid = 50389081 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 |
Glycogen synthase kinase-3 beta
(Homo sapiens (Human)) | BDBM50389081
(CHEMBL2064534)Show SMILES N#Cc1ccccc1-c1ccc(CSc2nnc(o2)-c2ccc3OCCOc3c2)cc1 Show InChI InChI=1S/C24H17N3O3S/c25-14-19-3-1-2-4-20(19)17-7-5-16(6-8-17)15-31-24-27-26-23(30-24)18-9-10-21-22(13-18)29-12-11-28-21/h1-10,13H,11-12,15H2 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | <5 | n/a | n/a | n/a | n/a | n/a | n/a |
Technische Universit£t Darmstadt
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GSK3beta using pIRS-1 as substrate preincubated for 15 mins |
J Med Chem 55: 4407-24 (2012)
Article DOI: 10.1021/jm300309a BindingDB Entry DOI: 10.7270/Q2MG7QK0 |
More data for this Ligand-Target Pair | |
Glycogen synthase kinase-3 alpha
(Homo sapiens (Human)) | BDBM50389081
(CHEMBL2064534)Show SMILES N#Cc1ccccc1-c1ccc(CSc2nnc(o2)-c2ccc3OCCOc3c2)cc1 Show InChI InChI=1S/C24H17N3O3S/c25-14-19-3-1-2-4-20(19)17-7-5-16(6-8-17)15-31-24-27-26-23(30-24)18-9-10-21-22(13-18)29-12-11-28-21/h1-10,13H,11-12,15H2 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | <5 | n/a | n/a | n/a | n/a | n/a | n/a |
Technische Universit£t Darmstadt
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GSK3alpha |
J Med Chem 55: 4407-24 (2012)
Article DOI: 10.1021/jm300309a BindingDB Entry DOI: 10.7270/Q2MG7QK0 |
More data for this Ligand-Target Pair | |
Casein kinase I isoform epsilon
(Homo sapiens (Human)) | BDBM50389081
(CHEMBL2064534)Show SMILES N#Cc1ccccc1-c1ccc(CSc2nnc(o2)-c2ccc3OCCOc3c2)cc1 Show InChI InChI=1S/C24H17N3O3S/c25-14-19-3-1-2-4-20(19)17-7-5-16(6-8-17)15-31-24-27-26-23(30-24)18-9-10-21-22(13-18)29-12-11-28-21/h1-10,13H,11-12,15H2 | PDB
KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Technische Universit£t Darmstadt
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CK1epsilon by FRET assay |
J Med Chem 55: 4407-24 (2012)
Article DOI: 10.1021/jm300309a BindingDB Entry DOI: 10.7270/Q2MG7QK0 |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50389081
(CHEMBL2064534)Show SMILES N#Cc1ccccc1-c1ccc(CSc2nnc(o2)-c2ccc3OCCOc3c2)cc1 Show InChI InChI=1S/C24H17N3O3S/c25-14-19-3-1-2-4-20(19)17-7-5-16(6-8-17)15-31-24-27-26-23(30-24)18-9-10-21-22(13-18)29-12-11-28-21/h1-10,13H,11-12,15H2 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Technische Universit£t Darmstadt
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p35 by FRET assay |
J Med Chem 55: 4407-24 (2012)
Article DOI: 10.1021/jm300309a BindingDB Entry DOI: 10.7270/Q2MG7QK0 |
More data for this Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50389081
(CHEMBL2064534)Show SMILES N#Cc1ccccc1-c1ccc(CSc2nnc(o2)-c2ccc3OCCOc3c2)cc1 Show InChI InChI=1S/C24H17N3O3S/c25-14-19-3-1-2-4-20(19)17-7-5-16(6-8-17)15-31-24-27-26-23(30-24)18-9-10-21-22(13-18)29-12-11-28-21/h1-10,13H,11-12,15H2 | 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 | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Technische Universit£t Darmstadt
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AurKA by FRET assay |
J Med Chem 55: 4407-24 (2012)
Article DOI: 10.1021/jm300309a BindingDB Entry DOI: 10.7270/Q2MG7QK0 |
More data for this Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50389081
(CHEMBL2064534)Show SMILES N#Cc1ccccc1-c1ccc(CSc2nnc(o2)-c2ccc3OCCOc3c2)cc1 Show InChI InChI=1S/C24H17N3O3S/c25-14-19-3-1-2-4-20(19)17-7-5-16(6-8-17)15-31-24-27-26-23(30-24)18-9-10-21-22(13-18)29-12-11-28-21/h1-10,13H,11-12,15H2 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Technische Universit£t Darmstadt
Curated by ChEMBL
| Assay Description Inhibition of human recombinant PKCalpha by FRET assay |
J Med Chem 55: 4407-24 (2012)
Article DOI: 10.1021/jm300309a BindingDB Entry DOI: 10.7270/Q2MG7QK0 |
More data for this Ligand-Target Pair | |