Found 3 hits for monomerid = 50161468 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 2
(Homo sapiens (Human)) | BDBM50161468
(CHEMBL3794127)Show SMILES [#6]\[#6](-[#6])=[#6](\c1ccccc1)-c1ccc(\[#6]=[#6]\[#6](=O)-[#7]-[#8])cc1 Show InChI InChI=1S/C19H19NO2/c1-14(2)19(16-6-4-3-5-7-16)17-11-8-15(9-12-17)10-13-18(21)20-22/h3-13,22H,1-2H3,(H,20,21)/b13-10+ | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
| PubMed
| n/a | n/a | 1.18E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Milan
Curated by ChEMBL
| Assay Description Inhibition of human recombinant HDAC2 using Fluor de Lys Green as substrate incubated for 30 mins by fluorescence assay |
Eur J Med Chem 112: 99-105 (2016)
BindingDB Entry DOI: 10.7270/Q2HM5BB0 |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50161468
(CHEMBL3794127)Show SMILES [#6]\[#6](-[#6])=[#6](\c1ccccc1)-c1ccc(\[#6]=[#6]\[#6](=O)-[#7]-[#8])cc1 Show InChI InChI=1S/C19H19NO2/c1-14(2)19(16-6-4-3-5-7-16)17-11-8-15(9-12-17)10-13-18(21)20-22/h3-13,22H,1-2H3,(H,20,21)/b13-10+ | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
| PubMed
| n/a | n/a | 2.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Milan
Curated by ChEMBL
| Assay Description Inhibition of HDAC in human HeLa nuclear extract using BOC-Ac-Lys-AMC as substrate incubated for 90 mins by fluorescence assay |
Eur J Med Chem 112: 99-105 (2016)
BindingDB Entry DOI: 10.7270/Q2HM5BB0 |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50161468
(CHEMBL3794127)Show SMILES [#6]\[#6](-[#6])=[#6](\c1ccccc1)-c1ccc(\[#6]=[#6]\[#6](=O)-[#7]-[#8])cc1 Show InChI InChI=1S/C19H19NO2/c1-14(2)19(16-6-4-3-5-7-16)17-11-8-15(9-12-17)10-13-18(21)20-22/h3-13,22H,1-2H3,(H,20,21)/b13-10+ | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
| PubMed
| n/a | n/a | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Milan
Curated by ChEMBL
| Assay Description Inhibition of HDAC in human HeLa cells using BOC-Ac-Lys-AMC as substrate incubated for 4 hrs by fluorescence assay |
Eur J Med Chem 112: 99-105 (2016)
BindingDB Entry DOI: 10.7270/Q2HM5BB0 |
More data for this Ligand-Target Pair | |