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BDBM50263460 CHEMBL4084164

SMILES: ONC(=O)\C=C\c1ccc(Cn2c3C4CCCC(=O)N4CCc3c3ccccc23)cc1

InChI Key: InChIKey=XIEDZYSMTIAQIH-OUKQBFOZSA-N

Data: 3 KI

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50263460   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Cereblon/Histone deacetylase 6


(Homo sapiens (Human))
BDBM50263460
PNG
(CHEMBL4084164)
Show SMILES ONC(=O)\C=C\c1ccc(Cn2c3C4CCCC(=O)N4CCc3c3ccccc23)cc1
Show InChI InChI=1S/C25H25N3O3/c29-23(26-31)13-12-17-8-10-18(11-9-17)16-28-21-5-2-1-4-19(21)20-14-15-27-22(25(20)28)6-3-7-24(27)30/h1-2,4-5,8-13,22,31H,3,6-7,14-16H2,(H,26,29)/b13-12+
PDB
MMDB

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PC cid
PC sid
UniChem
Article
PubMed
14n/an/an/an/an/an/an/an/a



Institute of Pharmacy, Faculty of Chemistry and Pharmacy , University of Regensburg , 93040 Regensburg , Germany.

Curated by ChEMBL


Assay Description
Inhibition of full length recombinant human N-terminal GST-tagged HDAC6 expressed in baculovirus-infected Sf9 insect cells using RHKK(Ac)AMC as subst...


J Med Chem 61: 3454-3477 (2018)


Article DOI: 10.1021/acs.jmedchem.7b01593
BindingDB Entry DOI: 10.7270/Q24B33S0
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50263460
PNG
(CHEMBL4084164)
Show SMILES ONC(=O)\C=C\c1ccc(Cn2c3C4CCCC(=O)N4CCc3c3ccccc23)cc1
Show InChI InChI=1S/C25H25N3O3/c29-23(26-31)13-12-17-8-10-18(11-9-17)16-28-21-5-2-1-4-19(21)20-14-15-27-22(25(20)28)6-3-7-24(27)30/h1-2,4-5,8-13,22,31H,3,6-7,14-16H2,(H,26,29)/b13-12+
PDB
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antibodypedia
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PC sid
UniChem
Article
PubMed
234n/an/an/an/an/an/an/an/a



Institute of Pharmacy, Faculty of Chemistry and Pharmacy , University of Regensburg , 93040 Regensburg , Germany.

Curated by ChEMBL


Assay Description
Inhibition of full length recombinant human C-terminal GST-tagged HDAC2 expressed in baculovirus-infected insect cells using RHKK(Ac)AMC as substrate...


J Med Chem 61: 3454-3477 (2018)


Article DOI: 10.1021/acs.jmedchem.7b01593
BindingDB Entry DOI: 10.7270/Q24B33S0
More data for this
Ligand-Target Pair
Histone deacetylase 8


(Homo sapiens (Human))
BDBM50263460
PNG
(CHEMBL4084164)
Show SMILES ONC(=O)\C=C\c1ccc(Cn2c3C4CCCC(=O)N4CCc3c3ccccc23)cc1
Show InChI InChI=1S/C25H25N3O3/c29-23(26-31)13-12-17-8-10-18(11-9-17)16-28-21-5-2-1-4-19(21)20-14-15-27-22(25(20)28)6-3-7-24(27)30/h1-2,4-5,8-13,22,31H,3,6-7,14-16H2,(H,26,29)/b13-12+
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
720n/an/an/an/an/an/an/an/a



Institute of Pharmacy, Faculty of Chemistry and Pharmacy , University of Regensburg , 93040 Regensburg , Germany.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human C-terminal His-tagged HDAC8 (1 to 377 residues) expressed in baculovirus-infected insect cells using RHK(Ac)K(Ac)AMC ...


J Med Chem 61: 3454-3477 (2018)


Article DOI: 10.1021/acs.jmedchem.7b01593
BindingDB Entry DOI: 10.7270/Q24B33S0
More data for this
Ligand-Target Pair