Found 5 hits of ic50 for monomerid = 50314631 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 1
(Homo sapiens (Human)) | BDBM50314631
![PNG](/data/jpeg/tenK5031/BindingDB_50314631.png) (CHEMBL1088949 | N-hydroxy-3-(2-(2-(2-methyl-1H-ind...)Show SMILES Cc1[nH]c2ccccc2c1CCN1Cc2ccc(\C=C\C(=O)NO)cc2C1 Show InChI InChI=1S/C22H23N3O2/c1-15-19(20-4-2-3-5-21(20)23-15)10-11-25-13-17-8-6-16(12-18(17)14-25)7-9-22(26)24-27/h2-9,12,23,27H,10-11,13-14H2,1H3,(H,24,26)/b9-7+ | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 26 | n/a | n/a | n/a | n/a | n/a | n/a |
Novartis Institutes for Biomedical Research
Curated by ChEMBL
| Assay Description Inhibition of purified recombinant HDAC1 |
Bioorg Med Chem Lett 21: 4909-12 (2011)
Article DOI: 10.1016/j.bmcl.2011.06.015 BindingDB Entry DOI: 10.7270/Q2542NZQ |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50314631
![PNG](/data/jpeg/tenK5031/BindingDB_50314631.png) (CHEMBL1088949 | N-hydroxy-3-(2-(2-(2-methyl-1H-ind...)Show SMILES Cc1[nH]c2ccccc2c1CCN1Cc2ccc(\C=C\C(=O)NO)cc2C1 Show InChI InChI=1S/C22H23N3O2/c1-15-19(20-4-2-3-5-21(20)23-15)10-11-25-13-17-8-6-16(12-18(17)14-25)7-9-22(26)24-27/h2-9,12,23,27H,10-11,13-14H2,1H3,(H,24,26)/b9-7+ | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 27 | n/a | n/a | n/a | n/a | n/a | n/a |
Novartis Institutes for Biomedical Research
Curated by ChEMBL
| Assay Description Inhibition of FLAG-tagged HDAC1 expressed in HEK293 cells by fluorescent assay |
J Med Chem 53: 2952-63 (2010)
Article DOI: 10.1021/jm100007m BindingDB Entry DOI: 10.7270/Q20V8CZC |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50314631
![PNG](/data/jpeg/tenK5031/BindingDB_50314631.png) (CHEMBL1088949 | N-hydroxy-3-(2-(2-(2-methyl-1H-ind...)Show SMILES Cc1[nH]c2ccccc2c1CCN1Cc2ccc(\C=C\C(=O)NO)cc2C1 Show InChI InChI=1S/C22H23N3O2/c1-15-19(20-4-2-3-5-21(20)23-15)10-11-25-13-17-8-6-16(12-18(17)14-25)7-9-22(26)24-27/h2-9,12,23,27H,10-11,13-14H2,1H3,(H,24,26)/b9-7+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 4.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Novartis Institutes for Biomedical Research
Curated by ChEMBL
| Assay Description Inhibition of human ERG by automated patch clamp assay |
Bioorg Med Chem Lett 21: 4909-12 (2011)
Article DOI: 10.1016/j.bmcl.2011.06.015 BindingDB Entry DOI: 10.7270/Q2542NZQ |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50314631
![PNG](/data/jpeg/tenK5031/BindingDB_50314631.png) (CHEMBL1088949 | N-hydroxy-3-(2-(2-(2-methyl-1H-ind...)Show SMILES Cc1[nH]c2ccccc2c1CCN1Cc2ccc(\C=C\C(=O)NO)cc2C1 Show InChI InChI=1S/C22H23N3O2/c1-15-19(20-4-2-3-5-21(20)23-15)10-11-25-13-17-8-6-16(12-18(17)14-25)7-9-22(26)24-27/h2-9,12,23,27H,10-11,13-14H2,1H3,(H,24,26)/b9-7+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 4.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Novartis Institutes for Biomedical Research
Curated by ChEMBL
| Assay Description Inhibition of human ERG expressed in CHO cells by automated patch clamp electrophisiology assay |
J Med Chem 53: 2952-63 (2010)
Article DOI: 10.1021/jm100007m BindingDB Entry DOI: 10.7270/Q20V8CZC |
More data for this Ligand-Target Pair | |
Cytochrome P450 3A4
(Homo sapiens (Human)) | BDBM50314631
![PNG](/data/jpeg/tenK5031/BindingDB_50314631.png) (CHEMBL1088949 | N-hydroxy-3-(2-(2-(2-methyl-1H-ind...)Show SMILES Cc1[nH]c2ccccc2c1CCN1Cc2ccc(\C=C\C(=O)NO)cc2C1 Show InChI InChI=1S/C22H23N3O2/c1-15-19(20-4-2-3-5-21(20)23-15)10-11-25-13-17-8-6-16(12-18(17)14-25)7-9-22(26)24-27/h2-9,12,23,27H,10-11,13-14H2,1H3,(H,24,26)/b9-7+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| 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 |
Novartis Institutes for Biomedical Research
Curated by ChEMBL
| Assay Description Inhibition of CYP3A4 |
Bioorg Med Chem Lett 21: 4909-12 (2011)
Article DOI: 10.1016/j.bmcl.2011.06.015 BindingDB Entry DOI: 10.7270/Q2542NZQ |
More data for this Ligand-Target Pair | |