Found 6 hits for monomerid = 50389084 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 |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50389084
(CHEMBL2064538)Show SMILES COC[C@@H]1COc2ccc(cc2O1)-c1nnc(SCc2ccc(cc2)-c2ccccc2C#N)o1 |r| Show InChI InChI=1S/C26H21N3O4S/c1-30-14-21-15-31-23-11-10-19(12-24(23)32-21)25-28-29-26(33-25)34-16-17-6-8-18(9-7-17)22-5-3-2-4-20(22)13-27/h2-12,21H,14-16H2,1H3/t21-/m1/s1 | 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 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 | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50389084
(CHEMBL2064538)Show SMILES COC[C@@H]1COc2ccc(cc2O1)-c1nnc(SCc2ccc(cc2)-c2ccccc2C#N)o1 |r| Show InChI InChI=1S/C26H21N3O4S/c1-30-14-21-15-31-23-11-10-19(12-24(23)32-21)25-28-29-26(33-25)34-16-17-6-8-18(9-7-17)22-5-3-2-4-20(22)13-27/h2-12,21H,14-16H2,1H3/t21-/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
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 | |
Glycogen synthase kinase-3 alpha
(Homo sapiens (Human)) | BDBM50389084
(CHEMBL2064538)Show SMILES COC[C@@H]1COc2ccc(cc2O1)-c1nnc(SCc2ccc(cc2)-c2ccccc2C#N)o1 |r| Show InChI InChI=1S/C26H21N3O4S/c1-30-14-21-15-31-23-11-10-19(12-24(23)32-21)25-28-29-26(33-25)34-16-17-6-8-18(9-7-17)22-5-3-2-4-20(22)13-27/h2-12,21H,14-16H2,1H3/t21-/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 195 | 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)) | BDBM50389084
(CHEMBL2064538)Show SMILES COC[C@@H]1COc2ccc(cc2O1)-c1nnc(SCc2ccc(cc2)-c2ccccc2C#N)o1 |r| Show InChI InChI=1S/C26H21N3O4S/c1-30-14-21-15-31-23-11-10-19(12-24(23)32-21)25-28-29-26(33-25)34-16-17-6-8-18(9-7-17)22-5-3-2-4-20(22)13-27/h2-12,21H,14-16H2,1H3/t21-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
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 | |
Glycogen synthase kinase-3 beta
(Homo sapiens (Human)) | BDBM50389084
(CHEMBL2064538)Show SMILES COC[C@@H]1COc2ccc(cc2O1)-c1nnc(SCc2ccc(cc2)-c2ccccc2C#N)o1 |r| Show InChI InChI=1S/C26H21N3O4S/c1-30-14-21-15-31-23-11-10-19(12-24(23)32-21)25-28-29-26(33-25)34-16-17-6-8-18(9-7-17)22-5-3-2-4-20(22)13-27/h2-12,21H,14-16H2,1H3/t21-/m1/s1 | 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 | 758 | 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 | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50389084
(CHEMBL2064538)Show SMILES COC[C@@H]1COc2ccc(cc2O1)-c1nnc(SCc2ccc(cc2)-c2ccccc2C#N)o1 |r| Show InChI InChI=1S/C26H21N3O4S/c1-30-14-21-15-31-23-11-10-19(12-24(23)32-21)25-28-29-26(33-25)34-16-17-6-8-18(9-7-17)22-5-3-2-4-20(22)13-27/h2-12,21H,14-16H2,1H3/t21-/m1/s1 | 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 | |