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Found 2 hits Enz. Inhib. hit(s) with Target = 'Histone deacetylase 3' and Ligand = 'BDBM323718'   
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 3


(Homo sapiens (Human))
BDBM323718
PNG
(US10188756, Compound CN149 | US11207431, Example B)
Show SMILES CN(Cc1ccc(\C=C\C(=O)NO)cc1F)CC12CC3CC(CC(C3)C1)C2 |TLB:20:21:25:19.24.18,24:19:26:25.23.22,24:23:26:19.20.18,THB:20:19:25:26.21.22|
Show InChI InChI=1S/C22H29FN2O2/c1-25(14-22-10-16-6-17(11-22)8-18(7-16)12-22)13-19-4-2-15(9-20(19)23)3-5-21(26)24-27/h2-5,9,16-18,27H,6-8,10-14H2,1H3,(H,24,26)/b5-3+
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UniProtKB/SwissProt

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DrugBank
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PC cid
PC sid
UniChem
US Patent
n/an/a 0.760n/an/an/an/an/an/a



The General Hospital Corporation

US Patent


Assay Description
All histone deacetylases were purchased from BPS Bioscience. The substrates, Broad Substrate A, and Broad Substrate B, were synthesized and are now a...


US Patent US10188756 (2019)


BindingDB Entry DOI: 10.7270/Q20Z75CX
More data for this
Ligand-Target Pair
Histone deacetylase 3


(Homo sapiens (Human))
BDBM323718
PNG
(US10188756, Compound CN149 | US11207431, Example B)
Show SMILES CN(Cc1ccc(\C=C\C(=O)NO)cc1F)CC12CC3CC(CC(C3)C1)C2 |TLB:20:21:25:19.24.18,24:19:26:25.23.22,24:23:26:19.20.18,THB:20:19:25:26.21.22|
Show InChI InChI=1S/C22H29FN2O2/c1-25(14-22-10-16-6-17(11-22)8-18(7-16)12-22)13-19-4-2-15(9-20(19)23)3-5-21(26)24-27/h2-5,9,16-18,27H,6-8,10-14H2,1H3,(H,24,26)/b5-3+
PDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 23n/an/an/an/an/an/a


TBA

Assay Description
IC50 measurements were conducted by BPS Biosciences (Table 1) or by Nanosyn (Table 1A) with an established fluorescence assay.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2639SXJ
More data for this
Ligand-Target Pair