Found 3 hits in this display 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 |
DNA polymerase alpha catalytic subunit
(Homo sapiens (Human)) | BDBM50184763
((3aS,4S,7R,7aR)-1,6-diethyl-2,7-bis(methoxycarbony...)Show SMILES CCC1=C(C(=O)OC)C(=O)[C@H]2[C@@H]1[C@@H](C(=O)OC)C(CC)=C[C@@H]2C(O)=O |c:2,20| Show InChI InChI=1S/C18H22O7/c1-5-8-7-10(16(20)21)13-12(11(8)17(22)24-3)9(6-2)14(15(13)19)18(23)25-4/h7,10-13H,5-6H2,1-4H3,(H,20,21)/t10-,11-,12-,13+/m0/s1 | 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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
The University of Manchester
Curated by ChEMBL
| Assay Description Inhibition of DNA polymerase alpha |
Bioorg Med Chem Lett 16: 2877-81 (2006)
Article DOI: 10.1016/j.bmcl.2006.03.005 BindingDB Entry DOI: 10.7270/Q25D8RF8 |
More data for this Ligand-Target Pair | |
DNA polymerase beta
(Homo sapiens (Human)) | BDBM50184763
((3aS,4S,7R,7aR)-1,6-diethyl-2,7-bis(methoxycarbony...)Show SMILES CCC1=C(C(=O)OC)C(=O)[C@H]2[C@@H]1[C@@H](C(=O)OC)C(CC)=C[C@@H]2C(O)=O |c:2,20| Show InChI InChI=1S/C18H22O7/c1-5-8-7-10(16(20)21)13-12(11(8)17(22)24-3)9(6-2)14(15(13)19)18(23)25-4/h7,10-13H,5-6H2,1-4H3,(H,20,21)/t10-,11-,12-,13+/m0/s1 | 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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
The University of Manchester
Curated by ChEMBL
| Assay Description Inhibition of DNA polymerase beta |
Bioorg Med Chem Lett 16: 2877-81 (2006)
Article DOI: 10.1016/j.bmcl.2006.03.005 BindingDB Entry DOI: 10.7270/Q25D8RF8 |
More data for this Ligand-Target Pair | |
DNA nucleotidylexotransferase
(Homo sapiens (Human)) | BDBM50184763
((3aS,4S,7R,7aR)-1,6-diethyl-2,7-bis(methoxycarbony...)Show SMILES CCC1=C(C(=O)OC)C(=O)[C@H]2[C@@H]1[C@@H](C(=O)OC)C(CC)=C[C@@H]2C(O)=O |c:2,20| Show InChI InChI=1S/C18H22O7/c1-5-8-7-10(16(20)21)13-12(11(8)17(22)24-3)9(6-2)14(15(13)19)18(23)25-4/h7,10-13H,5-6H2,1-4H3,(H,20,21)/t10-,11-,12-,13+/m0/s1 | PDB MMDB
NCI pathway KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
The University of Manchester
Curated by ChEMBL
| Assay Description Inhibition of human TdT |
Bioorg Med Chem Lett 16: 2877-81 (2006)
Article DOI: 10.1016/j.bmcl.2006.03.005 BindingDB Entry DOI: 10.7270/Q25D8RF8 |
More data for this Ligand-Target Pair | |