Found 7 hits for monomerid = 50137849 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 |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50137849
(6-(1,3-Dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-hexa...)Show SMILES Nc1ccccc1NC(=O)CCCCCN1C(=O)c2cccc3cccc(C1=O)c23 Show InChI InChI=1S/C24H23N3O3/c25-19-12-3-4-13-20(19)26-21(28)14-2-1-5-15-27-23(29)17-10-6-8-16-9-7-11-18(22(16)17)24(27)30/h3-4,6-13H,1-2,5,14-15,25H2,(H,26,28) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
MethylGene Inc.
Curated by ChEMBL
| Assay Description Ability to inhibit recombinant human histone deacetylase 1 (HDAC-1). |
Bioorg Med Chem Lett 14: 283-7 (2003)
BindingDB Entry DOI: 10.7270/Q2BV7G17 |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50137849
(6-(1,3-Dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-hexa...)Show SMILES Nc1ccccc1NC(=O)CCCCCN1C(=O)c2cccc3cccc(C1=O)c23 Show InChI InChI=1S/C24H23N3O3/c25-19-12-3-4-13-20(19)26-21(28)14-2-1-5-15-27-23(29)17-10-6-8-16-9-7-11-18(22(16)17)24(27)30/h3-4,6-13H,1-2,5,14-15,25H2,(H,26,28) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | n/a | n/a | 3.00E+3 | n/a | n/a | n/a | n/a |
MethylGene Inc.
Curated by ChEMBL
| Assay Description Effect on induced hyperacetylation of histones in whole cells |
Bioorg Med Chem Lett 14: 283-7 (2003)
BindingDB Entry DOI: 10.7270/Q2BV7G17 |
More data for this Ligand-Target Pair | |
Cereblon/Histone deacetylase 6
(Homo sapiens (Human)) | BDBM50137849
(6-(1,3-Dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-hexa...)Show SMILES Nc1ccccc1NC(=O)CCCCCN1C(=O)c2cccc3cccc(C1=O)c23 Show InChI InChI=1S/C24H23N3O3/c25-19-12-3-4-13-20(19)26-21(28)14-2-1-5-15-27-23(29)17-10-6-8-16-9-7-11-18(22(16)17)24(27)30/h3-4,6-13H,1-2,5,14-15,25H2,(H,26,28) | 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+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Deakin University
Curated by ChEMBL
| Assay Description Inhibition of recombinant N-terminal GST-tagged human HDAC6 (1 to 1215 residues) expressed in Baculovirus infected insect cells using RHKK-Ac as subs... |
Eur J Med Chem 162: 321-333 (2019)
Article DOI: 10.1016/j.ejmech.2018.11.020 |
More data for this Ligand-Target Pair | |
Histone deacetylase 11
(Homo sapiens (Human)) | BDBM50137849
(6-(1,3-Dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-hexa...)Show SMILES Nc1ccccc1NC(=O)CCCCCN1C(=O)c2cccc3cccc(C1=O)c23 Show InChI InChI=1S/C24H23N3O3/c25-19-12-3-4-13-20(19)26-21(28)14-2-1-5-15-27-23(29)17-10-6-8-16-9-7-11-18(22(16)17)24(27)30/h3-4,6-13H,1-2,5,14-15,25H2,(H,26,28) | NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 9.35E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Deakin University
Curated by ChEMBL
| Assay Description Inhibition of recombinant C-terminal His-tagged human HDAC11 (1 to 347 residues) expressed in Baculovirus infected insect cells using RHKK-Ac as subs... |
Eur J Med Chem 162: 321-333 (2019)
Article DOI: 10.1016/j.ejmech.2018.11.020 |
More data for this Ligand-Target Pair | |
Cereblon/Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50137849
(6-(1,3-Dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-hexa...)Show SMILES Nc1ccccc1NC(=O)CCCCCN1C(=O)c2cccc3cccc(C1=O)c23 Show InChI InChI=1S/C24H23N3O3/c25-19-12-3-4-13-20(19)26-21(28)14-2-1-5-15-27-23(29)17-10-6-8-16-9-7-11-18(22(16)17)24(27)30/h3-4,6-13H,1-2,5,14-15,25H2,(H,26,28) | 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 | 740 | n/a | n/a | n/a | n/a | n/a | n/a |
Deakin University
Curated by ChEMBL
| Assay Description Inhibition of recombinant full length C-terminal FLAG/His-tagged human HDAC1 (1 to 482 residues) expressed in sf21 cells using RHK-K(Ac)-AMC as subst... |
Eur J Med Chem 162: 321-333 (2019)
Article DOI: 10.1016/j.ejmech.2018.11.020 |
More data for this Ligand-Target Pair | |
Histone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2)
(Homo sapiens (Human)) | BDBM50137849
(6-(1,3-Dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-hexa...)Show SMILES Nc1ccccc1NC(=O)CCCCCN1C(=O)c2cccc3cccc(C1=O)c23 Show InChI InChI=1S/C24H23N3O3/c25-19-12-3-4-13-20(19)26-21(28)14-2-1-5-15-27-23(29)17-10-6-8-16-9-7-11-18(22(16)17)24(27)30/h3-4,6-13H,1-2,5,14-15,25H2,(H,26,28) | PDB
KEGG
UniProtKB/SwissProt
antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Deakin University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant full length C-terminal His-tagged HDAC3 (1 to 428 residues)/N-terminal GST-tagged NCOR2 (395 to 489 residues) express... |
Eur J Med Chem 162: 321-333 (2019)
Article DOI: 10.1016/j.ejmech.2018.11.020 |
More data for this Ligand-Target Pair | |
Histone deacetylase 8
(Homo sapiens (Human)) | BDBM50137849
(6-(1,3-Dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-hexa...)Show SMILES Nc1ccccc1NC(=O)CCCCCN1C(=O)c2cccc3cccc(C1=O)c23 Show InChI InChI=1S/C24H23N3O3/c25-19-12-3-4-13-20(19)26-21(28)14-2-1-5-15-27-23(29)17-10-6-8-16-9-7-11-18(22(16)17)24(27)30/h3-4,6-13H,1-2,5,14-15,25H2,(H,26,28) | 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+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Deakin University
Curated by ChEMBL
| Assay Description Inhibition of recombinant C-terminal His-tagged human HDAC8 (1 to 377 residues) expressed in Baculovirus infected insect cells using RHK-K(Ac)-AMC as... |
Eur J Med Chem 162: 321-333 (2019)
Article DOI: 10.1016/j.ejmech.2018.11.020 |
More data for this Ligand-Target Pair | |