Found 107 hits of Enzyme Inhibition Constant Data 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 |
|---|
Histone deacetylase 9
(Homo sapiens (Human)) | BDBM50319209
(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 6 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC9 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 4
(Homo sapiens (Human)) | BDBM50319209
(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 6 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC4 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 6
(Homo sapiens (Human)) | BDBM50319235
(6-(3-Benzoyl-ureido)-hexanoic acid hydroxyamide | ...)Show InChI InChI=1S/C14H19N3O4/c18-12(17-21)9-5-2-6-10-15-14(20)16-13(19)11-7-3-1-4-8-11/h1,3-4,7-8,21H,2,5-6,9-10H2,(H,17,18)(H2,15,16,19,20) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| 7 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC6 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 6
(Homo sapiens (Human)) | BDBM50319209
(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 8 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC6 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 3
(Homo sapiens (Human)) | BDBM50319209
(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 8 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC3 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319209
(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 8 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 11
(Homo sapiens (Human)) | BDBM50319209
(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 9 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC11 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Polyamine deacetylase HDAC10
(Homo sapiens (Human)) | BDBM50319209
(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 9 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC10 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 2
(Homo sapiens (Human)) | BDBM50319209
(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 12 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC2 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 5
(Homo sapiens (Human)) | BDBM50319209
(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 13 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC5 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319235
(6-(3-Benzoyl-ureido)-hexanoic acid hydroxyamide | ...)Show InChI InChI=1S/C14H19N3O4/c18-12(17-21)9-5-2-6-10-15-14(20)16-13(19)11-7-3-1-4-8-11/h1,3-4,7-8,21H,2,5-6,9-10H2,(H,17,18)(H2,15,16,19,20) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| 16 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 4
(Homo sapiens (Human)) | BDBM19149
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| 16 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC4 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 6
(Homo sapiens (Human)) | BDBM19149
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
Article
PubMed
| 18 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC6 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 4
(Homo sapiens (Human)) | BDBM50319235
(6-(3-Benzoyl-ureido)-hexanoic acid hydroxyamide | ...)Show InChI InChI=1S/C14H19N3O4/c18-12(17-21)9-5-2-6-10-15-14(20)16-13(19)11-7-3-1-4-8-11/h1,3-4,7-8,21H,2,5-6,9-10H2,(H,17,18)(H2,15,16,19,20) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| 20 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC4 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 3
(Homo sapiens (Human)) | BDBM50319235
(6-(3-Benzoyl-ureido)-hexanoic acid hydroxyamide | ...)Show InChI InChI=1S/C14H19N3O4/c18-12(17-21)9-5-2-6-10-15-14(20)16-13(19)11-7-3-1-4-8-11/h1,3-4,7-8,21H,2,5-6,9-10H2,(H,17,18)(H2,15,16,19,20) | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| 23 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC3 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 3
(Homo sapiens (Human)) | BDBM19149
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18) | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
Article
PubMed
| 29 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC3 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 6
(Homo sapiens (Human)) | BDBM50319209
(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 31 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC7 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 5
(Homo sapiens (Human)) | BDBM19149
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18) | KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| 33 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC5 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 11
(Homo sapiens (Human)) | BDBM19149
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18) | NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| 36 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC11 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 11
(Homo sapiens (Human)) | BDBM50319235
(6-(3-Benzoyl-ureido)-hexanoic acid hydroxyamide | ...)Show InChI InChI=1S/C14H19N3O4/c18-12(17-21)9-5-2-6-10-15-14(20)16-13(19)11-7-3-1-4-8-11/h1,3-4,7-8,21H,2,5-6,9-10H2,(H,17,18)(H2,15,16,19,20) | NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| 39 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC11 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Polyamine deacetylase HDAC10
(Homo sapiens (Human)) | BDBM50319235
(6-(3-Benzoyl-ureido)-hexanoic acid hydroxyamide | ...)Show InChI InChI=1S/C14H19N3O4/c18-12(17-21)9-5-2-6-10-15-14(20)16-13(19)11-7-3-1-4-8-11/h1,3-4,7-8,21H,2,5-6,9-10H2,(H,17,18)(H2,15,16,19,20) | NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| 40 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC10 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 2
(Homo sapiens (Human)) | BDBM19149
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
PDB
Article
PubMed
| 40 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC2 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Histone deacetylase 2
(Homo sapiens (Human)) | BDBM50319235
(6-(3-Benzoyl-ureido)-hexanoic acid hydroxyamide | ...)Show InChI InChI=1S/C14H19N3O4/c18-12(17-21)9-5-2-6-10-15-14(20)16-13(19)11-7-3-1-4-8-11/h1,3-4,7-8,21H,2,5-6,9-10H2,(H,17,18)(H2,15,16,19,20) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| 44 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC2 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 5
(Homo sapiens (Human)) | BDBM50319235
(6-(3-Benzoyl-ureido)-hexanoic acid hydroxyamide | ...)Show InChI InChI=1S/C14H19N3O4/c18-12(17-21)9-5-2-6-10-15-14(20)16-13(19)11-7-3-1-4-8-11/h1,3-4,7-8,21H,2,5-6,9-10H2,(H,17,18)(H2,15,16,19,20) | KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| 46 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC5 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Polyamine deacetylase HDAC10
(Homo sapiens (Human)) | BDBM19149
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18) | NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| 50 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC10 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 9
(Homo sapiens (Human)) | BDBM50319235
(6-(3-Benzoyl-ureido)-hexanoic acid hydroxyamide | ...)Show InChI InChI=1S/C14H19N3O4/c18-12(17-21)9-5-2-6-10-15-14(20)16-13(19)11-7-3-1-4-8-11/h1,3-4,7-8,21H,2,5-6,9-10H2,(H,17,18)(H2,15,16,19,20) | Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| 55 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC9 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM19149
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
PDB
Article
PubMed
| 63 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Histone deacetylase 9
(Homo sapiens (Human)) | BDBM19149
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18) | Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| 65 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC9 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 6
(Homo sapiens (Human)) | BDBM19149
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
Article
PubMed
| 126 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC7 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 8
(Homo sapiens (Human)) | BDBM19149
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
MMDB
PDB
Article
PubMed
| 205 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC8 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Histone deacetylase 8
(Homo sapiens (Human)) | BDBM50319235
(6-(3-Benzoyl-ureido)-hexanoic acid hydroxyamide | ...)Show InChI InChI=1S/C14H19N3O4/c18-12(17-21)9-5-2-6-10-15-14(20)16-13(19)11-7-3-1-4-8-11/h1,3-4,7-8,21H,2,5-6,9-10H2,(H,17,18)(H2,15,16,19,20) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| 252 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC8 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 8
(Homo sapiens (Human)) | BDBM50319235
(6-(3-Benzoyl-ureido)-hexanoic acid hydroxyamide | ...)Show InChI InChI=1S/C14H19N3O4/c18-12(17-21)9-5-2-6-10-15-14(20)16-13(19)11-7-3-1-4-8-11/h1,3-4,7-8,21H,2,5-6,9-10H2,(H,17,18)(H2,15,16,19,20) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| 252 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC8 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 8
(Homo sapiens (Human)) | BDBM50319209
(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 315 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC8 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319216
(6-[3-(Naphthalene-2-carbonyl)-ureido]-hexanoic aci...)Show InChI InChI=1S/C18H21N3O4/c22-16(21-25)8-2-1-5-11-19-18(24)20-17(23)15-10-9-13-6-3-4-7-14(13)12-15/h3-4,6-7,9-10,12,25H,1-2,5,8,11H2,(H,21,22)(H2,19,20,23,24) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 6 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319211
(6-[3-(4-Iodo-benzoyl)-ureido]-hexanoic acid hydrox...)Show InChI InChI=1S/C14H18IN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | 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 | 8 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319220
(6-[3-(3-amino-4-chloro-benzoyl)-ureido]-hexanoic a...)Show InChI InChI=1S/C14H19ClN4O4/c15-10-6-5-9(8-11(10)16)13(21)18-14(22)17-7-3-1-2-4-12(20)19-23/h5-6,8,23H,1-4,7,16H2,(H,19,20)(H2,17,18,21,22) | 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 | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319209
(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | 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 | 13 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319221
(6-[3-(3-Nitro-4-pyrrolidin-1-yl-benzoyl)-ureido]-h...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(N2CCCC2)c(c1)[N+]([O-])=O Show InChI InChI=1S/C18H25N5O6/c24-16(21-27)6-2-1-3-9-19-18(26)20-17(25)13-7-8-14(15(12-13)23(28)29)22-10-4-5-11-22/h7-8,12,27H,1-6,9-11H2,(H,21,24)(H2,19,20,25,26) | 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 | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319228
(6-{3-[1-(3-Phenyl-propyl)-1H-benzimidazole-5-carbo...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc2n(CCCc3ccccc3)cnc2c1 Show InChI InChI=1S/C24H29N5O4/c30-22(28-33)11-5-2-6-14-25-24(32)27-23(31)19-12-13-21-20(16-19)26-17-29(21)15-7-10-18-8-3-1-4-9-18/h1,3-4,8-9,12-13,16-17,33H,2,5-7,10-11,14-15H2,(H,28,30)(H2,25,27,31,32) | 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 | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319226
(6-{3-[4-(2-Diethylamino-ethylamino)-3-nitro-benzoy...)Show SMILES CCN(CC)CCNc1ccc(cc1[N+]([O-])=O)C(=O)NC(=O)NCCCCCC(=O)NO Show InChI InChI=1S/C20H32N6O6/c1-3-25(4-2)13-12-21-16-10-9-15(14-17(16)26(31)32)19(28)23-20(29)22-11-7-5-6-8-18(27)24-30/h9-10,14,21,30H,3-8,11-13H2,1-2H3,(H,24,27)(H2,22,23,28,29) | 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 | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319230
(6-{3-[1-(2-Diethylamino-ethyl)-1H-benzimidazole-5-...)Show SMILES CCN(CC)CCn1cnc2cc(ccc12)C(=O)NC(=O)NCCCCCC(=O)NO Show InChI InChI=1S/C21H32N6O4/c1-3-26(4-2)12-13-27-15-23-17-14-16(9-10-18(17)27)20(29)24-21(30)22-11-7-5-6-8-19(28)25-31/h9-10,14-15,31H,3-8,11-13H2,1-2H3,(H,25,28)(H2,22,24,29,30) | 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 | 21 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319212
(6-[3-(4-tert-Butyl-benzoyl)-ureido]-hexanoic acid ...)Show InChI InChI=1S/C18H27N3O4/c1-18(2,3)14-10-8-13(9-11-14)16(23)20-17(24)19-12-6-4-5-7-15(22)21-25/h8-11,25H,4-7,12H2,1-3H3,(H,21,22)(H2,19,20,23,24) | 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 | 24 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319208
(6-[3-(4-Chloro-benzoyl)-ureido]-hexanoic acid hydr...)Show InChI InChI=1S/C14H18ClN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | 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 | 26 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319219
(6-[3-(4-pyrimidin-5-yl-benzoyl)-ureido]-hexanoic a...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(cc1)-c1cncnc1 Show InChI InChI=1S/C18H21N5O4/c24-16(23-27)4-2-1-3-9-21-18(26)22-17(25)14-7-5-13(6-8-14)15-10-19-12-20-11-15/h5-8,10-12,27H,1-4,9H2,(H,23,24)(H2,21,22,25,26) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 26 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319232
(6-{3-[2-phenethyl-1-(2-pyrrolidin-1-yl-ethyl)-1H-b...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc2n(CCN3CCCC3)c(CCc3ccccc3)nc2c1 Show InChI InChI=1S/C29H38N6O4/c36-27(33-39)11-5-2-6-16-30-29(38)32-28(37)23-13-14-25-24(21-23)31-26(15-12-22-9-3-1-4-10-22)35(25)20-19-34-17-7-8-18-34/h1,3-4,9-10,13-14,21,39H,2,5-8,11-12,15-20H2,(H,33,36)(H2,30,32,37,38) | 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 | 34 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319217
(6-[3-(4-phenylacetylamino-benzoyl)-ureido]-hexanoi...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(NC(=O)Cc2ccccc2)cc1 Show InChI InChI=1S/C22H26N4O5/c27-19(26-31)9-5-2-6-14-23-22(30)25-21(29)17-10-12-18(13-11-17)24-20(28)15-16-7-3-1-4-8-16/h1,3-4,7-8,10-13,31H,2,5-6,9,14-15H2,(H,24,28)(H,26,27)(H2,23,25,29,30) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 44 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319213
(6-[3-(4-Nitro-benzoyl)-ureido]-hexanoic acid hydro...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(cc1)[N+]([O-])=O Show InChI InChI=1S/C14H18N4O6/c19-12(17-22)4-2-1-3-9-15-14(21)16-13(20)10-5-7-11(8-6-10)18(23)24/h5-8,22H,1-4,9H2,(H,17,19)(H2,15,16,20,21) | 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 | 45 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319224
(6-[3-(4-Morpholin-4-yl-3-nitro-benzoyl)-ureido]-he...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(N2CCOCC2)c(c1)[N+]([O-])=O Show InChI InChI=1S/C18H25N5O7/c24-16(21-27)4-2-1-3-7-19-18(26)20-17(25)13-5-6-14(15(12-13)23(28)29)22-8-10-30-11-9-22/h5-6,12,27H,1-4,7-11H2,(H,21,24)(H2,19,20,25,26) | 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 | 55 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319210
(6-[3-(3-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-6-4-5-10(9-11)13(20)17-14(21)16-8-3-1-2-7-12(19)18-22/h4-6,9,22H,1-3,7-8H2,(H,18,19)(H2,16,17,20,21) | 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 | 60 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319214
(6-[3-(3-Nitro-benzoyl)-ureido]-hexanoic acid hydro...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1cccc(c1)[N+]([O-])=O Show InChI InChI=1S/C14H18N4O6/c19-12(17-22)7-2-1-3-8-15-14(21)16-13(20)10-5-4-6-11(9-10)18(23)24/h4-6,9,22H,1-3,7-8H2,(H,17,19)(H2,15,16,20,21) | 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 | 92 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319237
(8-(3-Benzoyl-ureido)-octanoic acid hydroxyamide | ...)Show InChI InChI=1S/C16H23N3O4/c20-14(19-23)11-7-2-1-3-8-12-17-16(22)18-15(21)13-9-5-4-6-10-13/h4-6,9-10,23H,1-3,7-8,11-12H2,(H,19,20)(H2,17,18,21,22) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 97 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319218
(6-[3-(4-benzenesulfonylamino-benzoyl)-ureido]-hexa...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(NS(=O)(=O)c2ccccc2)cc1 Show InChI InChI=1S/C20H24N4O6S/c25-18(23-28)9-5-2-6-14-21-20(27)22-19(26)15-10-12-16(13-11-15)24-31(29,30)17-7-3-1-4-8-17/h1,3-4,7-8,10-13,24,28H,2,5-6,9,14H2,(H,23,25)(H2,21,22,26,27) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 97 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319207
(6-[3-(4-Fluoro-benzoyl)-ureido]-hexanoic acid hydr...)Show InChI InChI=1S/C14H18FN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | 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 | 115 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319236
(7-(3-Benzoyl-ureido)-heptanoic acid hydroxyamide |...)Show InChI InChI=1S/C15H21N3O4/c19-13(18-22)10-6-1-2-7-11-16-15(21)17-14(20)12-8-4-3-5-9-12/h3-5,8-9,22H,1-2,6-7,10-11H2,(H,18,19)(H2,16,17,20,21) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 145 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319215
(6-[3-(2,6-Dichloro-benzoyl)-ureido]-hexanoic acid ...)Show InChI InChI=1S/C14H17Cl2N3O4/c15-9-5-4-6-10(16)12(9)13(21)18-14(22)17-8-3-1-2-7-11(20)19-23/h4-6,23H,1-3,7-8H2,(H,19,20)(H2,17,18,21,22) | 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 | 185 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319205
(6-(3-Benzoyl-1-pyridin-2-ylmethyl-ureido)-hexanoic...)Show SMILES ONC(=O)CCCCCN(Cc1ccccn1)C(=O)NC(=O)c1ccccc1 Show InChI InChI=1S/C20H24N4O4/c25-18(23-28)12-5-2-8-14-24(15-17-11-6-7-13-21-17)20(27)22-19(26)16-9-3-1-4-10-16/h1,3-4,6-7,9-11,13,28H,2,5,8,12,14-15H2,(H,23,25)(H,22,26,27) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 245 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 8
(Homo sapiens (Human)) | BDBM50319236
(7-(3-Benzoyl-ureido)-heptanoic acid hydroxyamide |...)Show InChI InChI=1S/C15H21N3O4/c19-13(18-22)10-6-1-2-7-11-16-15(21)17-14(20)12-8-4-3-5-9-12/h3-5,8-9,22H,1-2,6-7,10-11H2,(H,18,19)(H2,16,17,20,21) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 270 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC8 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 8
(Homo sapiens (Human)) | BDBM19149
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
MMDB
PDB
Article
PubMed
| n/a | n/a | 272 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC8 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Histone deacetylase 8
(Homo sapiens (Human)) | BDBM50319238
(6-[3-benzoyl-1-(3-phenyl-propyl)-ureido]-hexanoic ...)Show SMILES ONC(=O)CCCCCN(CCCc1ccccc1)C(=O)NC(=O)c1ccccc1 Show InChI InChI=1S/C23H29N3O4/c27-21(25-30)16-8-3-9-17-26(18-10-13-19-11-4-1-5-12-19)23(29)24-22(28)20-14-6-2-7-15-20/h1-2,4-7,11-12,14-15,30H,3,8-10,13,16-18H2,(H,25,27)(H,24,28,29) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 328 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC8 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319239
(6-(3-benzoyl-1-benzyl-ureido)-hexanoic acid hydrox...)Show SMILES ONC(=O)CCCCCN(Cc1ccccc1)C(=O)NC(=O)c1ccccc1 Show InChI InChI=1S/C21H25N3O4/c25-19(23-28)14-8-3-9-15-24(16-17-10-4-1-5-11-17)21(27)22-20(26)18-12-6-2-7-13-18/h1-2,4-7,10-13,28H,3,8-9,14-16H2,(H,23,25)(H,22,26,27) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 355 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319238
(6-[3-benzoyl-1-(3-phenyl-propyl)-ureido]-hexanoic ...)Show SMILES ONC(=O)CCCCCN(CCCc1ccccc1)C(=O)NC(=O)c1ccccc1 Show InChI InChI=1S/C23H29N3O4/c27-21(25-30)16-8-3-9-17-26(18-10-13-19-11-4-1-5-12-19)23(29)24-22(28)20-14-6-2-7-15-20/h1-2,4-7,11-12,14-15,30H,3,8-10,13,16-18H2,(H,25,27)(H,24,28,29) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 392 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 8
(Homo sapiens (Human)) | BDBM50319237
(8-(3-Benzoyl-ureido)-octanoic acid hydroxyamide | ...)Show InChI InChI=1S/C16H23N3O4/c20-14(19-23)11-7-2-1-3-8-12-17-16(22)18-15(21)13-9-5-4-6-10-13/h4-6,9-10,23H,1-3,7-8,11-12H2,(H,19,20)(H2,17,18,21,22) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 405 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC8 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319206
(7-(3-Benzoyl-1-pyridin-2-ylmethyl-ureido)-heptanoi...)Show SMILES ONC(=O)CCCCCCN(Cc1ccccn1)C(=O)NC(=O)c1ccccc1 Show InChI InChI=1S/C21H26N4O4/c26-19(24-29)13-6-1-2-9-15-25(16-18-12-7-8-14-22-18)21(28)23-20(27)17-10-4-3-5-11-17/h3-5,7-8,10-12,14,29H,1-2,6,9,13,15-16H2,(H,24,26)(H,23,27,28) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 555 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319209
(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | 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 | 870 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319211
(6-[3-(4-Iodo-benzoyl)-ureido]-hexanoic acid hydrox...)Show InChI InChI=1S/C14H18IN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | 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 | 870 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319220
(6-[3-(3-amino-4-chloro-benzoyl)-ureido]-hexanoic a...)Show InChI InChI=1S/C14H19ClN4O4/c15-10-6-5-9(8-11(10)16)13(21)18-14(22)17-7-3-1-2-4-12(20)19-23/h5-6,8,23H,1-4,7,16H2,(H,19,20)(H2,17,18,21,22) | 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 | 1.25E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319208
(6-[3-(4-Chloro-benzoyl)-ureido]-hexanoic acid hydr...)Show InChI InChI=1S/C14H18ClN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | 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 | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319240
(7-(3-Benzoyl-1-benzyl-ureido)-heptanoic acid hydro...)Show SMILES ONC(=O)CCCCCCN(Cc1ccccc1)C(=O)NC(=O)c1ccccc1 Show InChI InChI=1S/C22H27N3O4/c26-20(24-29)15-9-1-2-10-16-25(17-18-11-5-3-6-12-18)22(28)23-21(27)19-13-7-4-8-14-19/h3-8,11-14,29H,1-2,9-10,15-17H2,(H,24,26)(H,23,27,28) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319226
(6-{3-[4-(2-Diethylamino-ethylamino)-3-nitro-benzoy...)Show SMILES CCN(CC)CCNc1ccc(cc1[N+]([O-])=O)C(=O)NC(=O)NCCCCCC(=O)NO Show InChI InChI=1S/C20H32N6O6/c1-3-25(4-2)13-12-21-16-10-9-15(14-17(16)26(31)32)19(28)23-20(29)22-11-7-5-6-8-18(27)24-30/h9-10,14,21,30H,3-8,11-13H2,1-2H3,(H,24,27)(H2,22,23,28,29) | 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 | 1.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319216
(6-[3-(Naphthalene-2-carbonyl)-ureido]-hexanoic aci...)Show InChI InChI=1S/C18H21N3O4/c22-16(21-25)8-2-1-5-11-19-18(24)20-17(23)15-10-9-13-6-3-4-7-14(13)12-15/h3-4,6-7,9-10,12,25H,1-2,5,8,11H2,(H,21,22)(H2,19,20,23,24) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 2.15E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM19149
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
PDB
Article
PubMed
| n/a | n/a | 2.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319235
(6-(3-Benzoyl-ureido)-hexanoic acid hydroxyamide | ...)Show InChI InChI=1S/C14H19N3O4/c18-12(17-21)9-5-2-6-10-15-14(20)16-13(19)11-7-3-1-4-8-11/h1,3-4,7-8,21H,2,5-6,9-10H2,(H,17,18)(H2,15,16,19,20) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 2.21E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319213
(6-[3-(4-Nitro-benzoyl)-ureido]-hexanoic acid hydro...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(cc1)[N+]([O-])=O Show InChI InChI=1S/C14H18N4O6/c19-12(17-22)4-2-1-3-9-15-14(21)16-13(20)10-5-7-11(8-6-10)18(23)24/h5-8,22H,1-4,9H2,(H,17,19)(H2,15,16,20,21) | 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 | 2.31E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319212
(6-[3-(4-tert-Butyl-benzoyl)-ureido]-hexanoic acid ...)Show InChI InChI=1S/C18H27N3O4/c1-18(2,3)14-10-8-13(9-11-14)16(23)20-17(24)19-12-6-4-5-7-15(22)21-25/h8-11,25H,4-7,12H2,1-3H3,(H,21,22)(H2,19,20,23,24) | 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 | 2.35E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319225
(6-{3-[3-nitro-4-(2-pyrrolidin-1-yl-ethylamino)-ben...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(NCCN2CCCC2)c(c1)[N+]([O-])=O Show InChI InChI=1S/C20H30N6O6/c27-18(24-30)6-2-1-3-9-22-20(29)23-19(28)15-7-8-16(17(14-15)26(31)32)21-10-13-25-11-4-5-12-25/h7-8,14,21,30H,1-6,9-13H2,(H,24,27)(H2,22,23,28,29) | 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 | 2.42E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319225
(6-{3-[3-nitro-4-(2-pyrrolidin-1-yl-ethylamino)-ben...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(NCCN2CCCC2)c(c1)[N+]([O-])=O Show InChI InChI=1S/C20H30N6O6/c27-18(24-30)6-2-1-3-9-22-20(29)23-19(28)15-7-8-16(17(14-15)26(31)32)21-10-13-25-11-4-5-12-25/h7-8,14,21,30H,1-6,9-13H2,(H,24,27)(H2,22,23,28,29) | 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 | 2.42E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319207
(6-[3-(4-Fluoro-benzoyl)-ureido]-hexanoic acid hydr...)Show InChI InChI=1S/C14H18FN3O4/c15-11-7-5-10(6-8-11)13(20)17-14(21)16-9-3-1-2-4-12(19)18-22/h5-8,22H,1-4,9H2,(H,18,19)(H2,16,17,20,21) | 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 | 2.55E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319236
(7-(3-Benzoyl-ureido)-heptanoic acid hydroxyamide |...)Show InChI InChI=1S/C15H21N3O4/c19-13(18-22)10-6-1-2-7-11-16-15(21)17-14(20)12-8-4-3-5-9-12/h3-5,8-9,22H,1-2,6-7,10-11H2,(H,18,19)(H2,16,17,20,21) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 2.68E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319214
(6-[3-(3-Nitro-benzoyl)-ureido]-hexanoic acid hydro...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1cccc(c1)[N+]([O-])=O Show InChI InChI=1S/C14H18N4O6/c19-12(17-22)7-2-1-3-8-15-14(21)16-13(20)10-5-4-6-11(9-10)18(23)24/h4-6,9,22H,1-3,7-8H2,(H,17,19)(H2,15,16,20,21) | 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 | 2.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319233
(6-{3-[2-Butyl-1-(2-pyrrolidin-1-yl-ethyl)-1H-benzi...)Show SMILES CCCCc1nc2cc(ccc2n1CCN1CCCC1)C(=O)NC(=O)NCCCCCC(=O)NO Show InChI InChI=1S/C25H38N6O4/c1-2-3-9-22-27-20-18-19(11-12-21(20)31(22)17-16-30-14-7-8-15-30)24(33)28-25(34)26-13-6-4-5-10-23(32)29-35/h11-12,18,35H,2-10,13-17H2,1H3,(H,29,32)(H2,26,28,33,34) | 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 | 2.91E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319233
(6-{3-[2-Butyl-1-(2-pyrrolidin-1-yl-ethyl)-1H-benzi...)Show SMILES CCCCc1nc2cc(ccc2n1CCN1CCCC1)C(=O)NC(=O)NCCCCCC(=O)NO Show InChI InChI=1S/C25H38N6O4/c1-2-3-9-22-27-20-18-19(11-12-21(20)31(22)17-16-30-14-7-8-15-30)24(33)28-25(34)26-13-6-4-5-10-23(32)29-35/h11-12,18,35H,2-10,13-17H2,1H3,(H,29,32)(H2,26,28,33,34) | 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 | 2.91E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319215
(6-[3-(2,6-Dichloro-benzoyl)-ureido]-hexanoic acid ...)Show InChI InChI=1S/C14H17Cl2N3O4/c15-9-5-4-6-10(16)12(9)13(21)18-14(22)17-8-3-1-2-7-11(20)19-23/h4-6,23H,1-3,7-8H2,(H,19,20)(H2,17,18,21,22) | 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 | 2.95E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319210
(6-[3-(3-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)Show InChI InChI=1S/C14H18BrN3O4/c15-11-6-4-5-10(9-11)13(20)17-14(21)16-8-3-1-2-7-12(19)18-22/h4-6,9,22H,1-3,7-8H2,(H,18,19)(H2,16,17,20,21) | 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 | 3.15E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319239
(6-(3-benzoyl-1-benzyl-ureido)-hexanoic acid hydrox...)Show SMILES ONC(=O)CCCCCN(Cc1ccccc1)C(=O)NC(=O)c1ccccc1 Show InChI InChI=1S/C21H25N3O4/c25-19(23-28)14-8-3-9-15-24(16-17-10-4-1-5-11-17)21(27)22-20(26)18-12-6-2-7-13-18/h1-2,4-7,10-13,28H,3,8-9,14-16H2,(H,23,25)(H,22,26,27) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 3.19E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319222
(6-[3-(3-Nitro-4-piperidin-1-yl-benzoyl)-ureido]-he...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(N2CCCCC2)c(c1)[N+]([O-])=O Show InChI InChI=1S/C19H27N5O6/c25-17(22-28)7-3-1-4-10-20-19(27)21-18(26)14-8-9-15(16(13-14)24(29)30)23-11-5-2-6-12-23/h8-9,13,28H,1-7,10-12H2,(H,22,25)(H2,20,21,26,27) | 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 | 3.25E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319222
(6-[3-(3-Nitro-4-piperidin-1-yl-benzoyl)-ureido]-he...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(N2CCCCC2)c(c1)[N+]([O-])=O Show InChI InChI=1S/C19H27N5O6/c25-17(22-28)7-3-1-4-10-20-19(27)21-18(26)14-8-9-15(16(13-14)24(29)30)23-11-5-2-6-12-23/h8-9,13,28H,1-7,10-12H2,(H,22,25)(H2,20,21,26,27) | 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 | 3.25E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319221
(6-[3-(3-Nitro-4-pyrrolidin-1-yl-benzoyl)-ureido]-h...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(N2CCCC2)c(c1)[N+]([O-])=O Show InChI InChI=1S/C18H25N5O6/c24-16(21-27)6-2-1-3-9-19-18(26)20-17(25)13-7-8-14(15(12-13)23(28)29)22-10-4-5-11-22/h7-8,12,27H,1-6,9-11H2,(H,21,24)(H2,19,20,25,26) | 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 | 3.45E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319231
(6-{3-[1-(3-Dimethylamino-2,2-dimethyl-propyl)-1H-b...)Show SMILES CN(C)CC(C)(C)Cn1cnc2cc(ccc12)C(=O)NC(=O)NCCCCCC(=O)NO Show InChI InChI=1S/C22H34N6O4/c1-22(2,13-27(3)4)14-28-15-24-17-12-16(9-10-18(17)28)20(30)25-21(31)23-11-7-5-6-8-19(29)26-32/h9-10,12,15,32H,5-8,11,13-14H2,1-4H3,(H,26,29)(H2,23,25,30,31) | 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 | 3.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319231
(6-{3-[1-(3-Dimethylamino-2,2-dimethyl-propyl)-1H-b...)Show SMILES CN(C)CC(C)(C)Cn1cnc2cc(ccc12)C(=O)NC(=O)NCCCCCC(=O)NO Show InChI InChI=1S/C22H34N6O4/c1-22(2,13-27(3)4)14-28-15-24-17-12-16(9-10-18(17)28)20(30)25-21(31)23-11-7-5-6-8-19(29)26-32/h9-10,12,15,32H,5-8,11,13-14H2,1-4H3,(H,26,29)(H2,23,25,30,31) | 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 | 3.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319228
(6-{3-[1-(3-Phenyl-propyl)-1H-benzimidazole-5-carbo...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc2n(CCCc3ccccc3)cnc2c1 Show InChI InChI=1S/C24H29N5O4/c30-22(28-33)11-5-2-6-14-25-24(32)27-23(31)19-12-13-21-20(16-19)26-17-29(21)15-7-10-18-8-3-1-4-9-18/h1,3-4,8-9,12-13,16-17,33H,2,5-7,10-11,14-15H2,(H,28,30)(H2,25,27,31,32) | 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 | 3.75E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319230
(6-{3-[1-(2-Diethylamino-ethyl)-1H-benzimidazole-5-...)Show SMILES CCN(CC)CCn1cnc2cc(ccc12)C(=O)NC(=O)NCCCCCC(=O)NO Show InChI InChI=1S/C21H32N6O4/c1-3-26(4-2)12-13-27-15-23-17-14-16(9-10-18(17)27)20(29)24-21(30)22-11-7-5-6-8-19(28)25-31/h9-10,14-15,31H,3-8,11-13H2,1-2H3,(H,25,28)(H2,22,24,29,30) | 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 | 5.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319232
(6-{3-[2-phenethyl-1-(2-pyrrolidin-1-yl-ethyl)-1H-b...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc2n(CCN3CCCC3)c(CCc3ccccc3)nc2c1 Show InChI InChI=1S/C29H38N6O4/c36-27(33-39)11-5-2-6-16-30-29(38)32-28(37)23-13-14-25-24(21-23)31-26(15-12-22-9-3-1-4-10-22)35(25)20-19-34-17-7-8-18-34/h1,3-4,9-10,13-14,21,39H,2,5-8,11-12,15-20H2,(H,33,36)(H2,30,32,37,38) | 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 | 5.38E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319237
(8-(3-Benzoyl-ureido)-octanoic acid hydroxyamide | ...)Show InChI InChI=1S/C16H23N3O4/c20-14(19-23)11-7-2-1-3-8-12-17-16(22)18-15(21)13-9-5-4-6-10-13/h4-6,9-10,23H,1-3,7-8,11-12H2,(H,19,20)(H2,17,18,21,22) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 8.28E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319206
(7-(3-Benzoyl-1-pyridin-2-ylmethyl-ureido)-heptanoi...)Show SMILES ONC(=O)CCCCCCN(Cc1ccccn1)C(=O)NC(=O)c1ccccc1 Show InChI InChI=1S/C21H26N4O4/c26-19(24-29)13-6-1-2-9-15-25(16-18-12-7-8-14-22-18)21(28)23-20(27)17-10-4-3-5-11-17/h3-5,7-8,10-12,14,29H,1-2,6,9,13,15-16H2,(H,24,26)(H,23,27,28) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 9.06E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319227
(6-[3-(1-Phenethyl-1H-benzimidazole-5-carbonyl)-ure...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc2n(CCc3ccccc3)cnc2c1 Show InChI InChI=1S/C23H27N5O4/c29-21(27-32)9-5-2-6-13-24-23(31)26-22(30)18-10-11-20-19(15-18)25-16-28(20)14-12-17-7-3-1-4-8-17/h1,3-4,7-8,10-11,15-16,32H,2,5-6,9,12-14H2,(H,27,29)(H2,24,26,30,31) | 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 | 9.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319227
(6-[3-(1-Phenethyl-1H-benzimidazole-5-carbonyl)-ure...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc2n(CCc3ccccc3)cnc2c1 Show InChI InChI=1S/C23H27N5O4/c29-21(27-32)9-5-2-6-13-24-23(31)26-22(30)18-10-11-20-19(15-18)25-16-28(20)14-12-17-7-3-1-4-8-17/h1,3-4,7-8,10-11,15-16,32H,2,5-6,9,12-14H2,(H,27,29)(H2,24,26,30,31) | 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 | 9.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319219
(6-[3-(4-pyrimidin-5-yl-benzoyl)-ureido]-hexanoic a...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(cc1)-c1cncnc1 Show InChI InChI=1S/C18H21N5O4/c24-16(23-27)4-2-1-3-9-21-18(26)22-17(25)14-7-5-13(6-8-14)15-10-19-12-20-11-15/h5-8,10-12,27H,1-4,9H2,(H,23,24)(H2,21,22,25,26) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319234
(4-(3-Benzoyl-ureido)-N-hydroxy-butyramide | CHEMBL...)Show InChI InChI=1S/C12H15N3O4/c16-10(15-19)7-4-8-13-12(18)14-11(17)9-5-2-1-3-6-9/h1-3,5-6,19H,4,7-8H2,(H,15,16)(H2,13,14,17,18) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 8
(Homo sapiens (Human)) | BDBM50319234
(4-(3-Benzoyl-ureido)-N-hydroxy-butyramide | CHEMBL...)Show InChI InChI=1S/C12H15N3O4/c16-10(15-19)7-4-8-13-12(18)14-11(17)9-5-2-1-3-6-9/h1-3,5-6,19H,4,7-8H2,(H,15,16)(H2,13,14,17,18) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC8 |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319223
(6-{3-[4-(4-Methyl-piperazin-1-yl)-3-nitro-benzoyl]...)Show SMILES CN1CCN(CC1)c1ccc(cc1[N+]([O-])=O)C(=O)NC(=O)NCCCCCC(=O)NO Show InChI InChI=1S/C19H28N6O6/c1-23-9-11-24(12-10-23)15-7-6-14(13-16(15)25(30)31)18(27)21-19(28)20-8-4-2-3-5-17(26)22-29/h6-7,13,29H,2-5,8-12H2,1H3,(H,22,26)(H2,20,21,27,28) | 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 | 1.15E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319223
(6-{3-[4-(4-Methyl-piperazin-1-yl)-3-nitro-benzoyl]...)Show SMILES CN1CCN(CC1)c1ccc(cc1[N+]([O-])=O)C(=O)NC(=O)NCCCCCC(=O)NO Show InChI InChI=1S/C19H28N6O6/c1-23-9-11-24(12-10-23)15-7-6-14(13-16(15)25(30)31)18(27)21-19(28)20-8-4-2-3-5-17(26)22-29/h6-7,13,29H,2-5,8-12H2,1H3,(H,22,26)(H2,20,21,27,28) | 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 | 1.15E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319224
(6-[3-(4-Morpholin-4-yl-3-nitro-benzoyl)-ureido]-he...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(N2CCOCC2)c(c1)[N+]([O-])=O Show InChI InChI=1S/C18H25N5O7/c24-16(21-27)4-2-1-3-7-19-18(26)20-17(25)13-5-6-14(15(12-13)23(28)29)22-8-10-30-11-9-22/h5-6,12,27H,1-4,7-11H2,(H,21,24)(H2,19,20,25,26) | 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 | 1.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319217
(6-[3-(4-phenylacetylamino-benzoyl)-ureido]-hexanoi...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(NC(=O)Cc2ccccc2)cc1 Show InChI InChI=1S/C22H26N4O5/c27-19(26-31)9-5-2-6-14-23-22(30)25-21(29)17-10-12-18(13-11-17)24-20(28)15-16-7-3-1-4-8-16/h1,3-4,7-8,10-13,31H,2,5-6,9,14-15H2,(H,24,28)(H,26,27)(H2,23,25,29,30) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 1.32E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319205
(6-(3-Benzoyl-1-pyridin-2-ylmethyl-ureido)-hexanoic...)Show SMILES ONC(=O)CCCCCN(Cc1ccccn1)C(=O)NC(=O)c1ccccc1 Show InChI InChI=1S/C20H24N4O4/c25-18(23-28)12-5-2-8-14-24(15-17-11-6-7-13-21-17)20(27)22-19(26)16-9-3-1-4-10-16/h1,3-4,6-7,9-11,13,28H,2,5,8,12,14-15H2,(H,23,25)(H,22,26,27) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 1.47E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319229
(6-{3-[1-(2-Dimethylamino-ethyl)-1H-benzimidazole-5...)Show SMILES CN(C)CCn1cnc2cc(ccc12)C(=O)NC(=O)NCCCCCC(=O)NO Show InChI InChI=1S/C19H28N6O4/c1-24(2)10-11-25-13-21-15-12-14(7-8-16(15)25)18(27)22-19(28)20-9-5-3-4-6-17(26)23-29/h7-8,12-13,29H,3-6,9-11H2,1-2H3,(H,23,26)(H2,20,22,27,28) | 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 | 1.95E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319229
(6-{3-[1-(2-Dimethylamino-ethyl)-1H-benzimidazole-5...)Show SMILES CN(C)CCn1cnc2cc(ccc12)C(=O)NC(=O)NCCCCCC(=O)NO Show InChI InChI=1S/C19H28N6O4/c1-24(2)10-11-25-13-21-15-12-14(7-8-16(15)25)18(27)22-19(28)20-9-5-3-4-6-17(26)23-29/h7-8,12-13,29H,3-6,9-11H2,1-2H3,(H,23,26)(H2,20,22,27,28) | 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 | 1.95E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50319218
(6-[3-(4-benzenesulfonylamino-benzoyl)-ureido]-hexa...)Show SMILES ONC(=O)CCCCCNC(=O)NC(=O)c1ccc(NS(=O)(=O)c2ccccc2)cc1 Show InChI InChI=1S/C20H24N4O6S/c25-18(23-28)9-5-2-6-14-21-20(27)22-19(26)15-10-12-16(13-11-15)24-31(29,30)17-7-3-1-4-8-17/h1,3-4,7-8,10-13,24,28H,2,5-6,9,14H2,(H,23,25)(H2,21,22,26,27) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
S *BIO Pte Ltd
Curated by ChEMBL
| Assay Description
Inhibition of HDAC1 in human COLO205 cells assessed as induction of histone H3 acetylation |
Bioorg Med Chem Lett 20: 3314-21 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.041
BindingDB Entry DOI: 10.7270/Q2GT5NCX |
More data for this
Ligand-Target Pair | |
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