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Compile Data Set for Download or QSAR

Found 4 hits of ic50 for monomerid = 50351943   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Histone deacetylase 6


(Homo sapiens (Human))
BDBM50351943
PNG
(CHEMBL1822042)
Show SMILES CC(C)CCc1c(O)c(CCC(=O)NO)ccc1OCCCCCCC(=O)NO
Show InChI InChI=1S/C21H34N2O6/c1-15(2)8-11-17-18(29-14-6-4-3-5-7-19(24)22-27)12-9-16(21(17)26)10-13-20(25)23-28/h9,12,15,26-28H,3-8,10-11,13-14H2,1-2H3,(H,22,24)(H,23,25)
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Article
PubMed
n/an/a 15.9n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL


Assay Description
Inhibition of HDAC6 using Boc-Lys(Ac)-AMC as substrate incubated 30 mins before substrate addition measured after 30 mins post substrate addition by ...


Eur J Med Chem 46: 4042-9 (2011)


Article DOI: 10.1016/j.ejmech.2011.06.002
BindingDB Entry DOI: 10.7270/Q2ZS2WWD
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50351943
PNG
(CHEMBL1822042)
Show SMILES CC(C)CCc1c(O)c(CCC(=O)NO)ccc1OCCCCCCC(=O)NO
Show InChI InChI=1S/C21H34N2O6/c1-15(2)8-11-17-18(29-14-6-4-3-5-7-19(24)22-27)12-9-16(21(17)26)10-13-20(25)23-28/h9,12,15,26-28H,3-8,10-11,13-14H2,1-2H3,(H,22,24)(H,23,25)
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Article
PubMed
n/an/a 42.9n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL


Assay Description
Inhibition of HDAC1 using KI-177 as substrate incubated 30 mins before substrate addition measured after 30 mins post substrate addition by fluoresce...


Eur J Med Chem 46: 4042-9 (2011)


Article DOI: 10.1016/j.ejmech.2011.06.002
BindingDB Entry DOI: 10.7270/Q2ZS2WWD
More data for this
Ligand-Target Pair
Histone deacetylase 8


(Homo sapiens (Human))
BDBM50351943
PNG
(CHEMBL1822042)
Show SMILES CC(C)CCc1c(O)c(CCC(=O)NO)ccc1OCCCCCCC(=O)NO
Show InChI InChI=1S/C21H34N2O6/c1-15(2)8-11-17-18(29-14-6-4-3-5-7-19(24)22-27)12-9-16(21(17)26)10-13-20(25)23-28/h9,12,15,26-28H,3-8,10-11,13-14H2,1-2H3,(H,22,24)(H,23,25)
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Article
PubMed
n/an/a 268n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL


Assay Description
Inhibition of human HDAC8 using Boc-Lys(TFA)-AMC as substrate incubated 30 mins before substrate addition measured after 30 mins post substrate addit...


Eur J Med Chem 46: 4042-9 (2011)


Article DOI: 10.1016/j.ejmech.2011.06.002
BindingDB Entry DOI: 10.7270/Q2ZS2WWD
More data for this
Ligand-Target Pair
Histone deacetylase 4


(Homo sapiens (Human))
BDBM50351943
PNG
(CHEMBL1822042)
Show SMILES CC(C)CCc1c(O)c(CCC(=O)NO)ccc1OCCCCCCC(=O)NO
Show InChI InChI=1S/C21H34N2O6/c1-15(2)8-11-17-18(29-14-6-4-3-5-7-19(24)22-27)12-9-16(21(17)26)10-13-20(25)23-28/h9,12,15,26-28H,3-8,10-11,13-14H2,1-2H3,(H,22,24)(H,23,25)
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KEGG

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Article
PubMed
n/an/a>1.00E+4n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL


Assay Description
Inhibition of HDAC4 using Boc-Lys(TFA)-AMC as substrate incubated 30 mins before substrate addition measured after 30 mins post substrate addition by...


Eur J Med Chem 46: 4042-9 (2011)


Article DOI: 10.1016/j.ejmech.2011.06.002
BindingDB Entry DOI: 10.7270/Q2ZS2WWD
More data for this
Ligand-Target Pair