BDBM50354088 CHEMBL1836142

SMILES CC[C@H](C)[C@H]1NC(=O)[C@H]2CSSCC\C=C\[C@H](CC(=O)N[C@H](CCSC)C(=O)N2)OC(=O)C[C@@H]1O

InChI Key InChIKey=VJXBYUITQBTTQM-UHFFFAOYSA-N

Data  10 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 50354088   

TargetHistone deacetylase 7(Human)
University of Wisconsin-Milwaukee

Curated by ChEMBL
LigandPNGBDBM50354088(CHEMBL1836142)
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of recombinant human HDAC7 using Boc-L-Lys(epsilon-trifluoroacetyl)-AMC as substrate by two-step fluorogenic assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/24/2012
Entry Details Article
PubMed
TargetHistone deacetylase 8(Human)
University of Wisconsin-Milwaukee

Curated by ChEMBL
LigandPNGBDBM50354088(CHEMBL1836142)
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of recombinant human HDAC8 using Boc-L-Lys(epsilon-trifluoroacetyl)-AMC as substrate by two-step fluorogenic assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/24/2012
Entry Details Article
PubMed
TargetHistone deacetylase 9(Human)
University of Wisconsin-Milwaukee

Curated by ChEMBL
LigandPNGBDBM50354088(CHEMBL1836142)
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of recombinant human HDAC9 using Boc-L-Lys(epsilon-trifluoroacetyl)-AMC as substrate by two-step fluorogenic assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/24/2012
Entry Details Article
PubMed
TargetHistone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2)(Human)
University of Wisconsin-Milwaukee

Curated by ChEMBL
LigandPNGBDBM50354088(CHEMBL1836142)
Affinity DataIC50: 87nMAssay Description:Inhibition of recombinant human HDAC3/NCOR2 using Boc-L-Lys(epsilon-trifluoroacetyl)-AMC as substrate by two-step fluorogenic assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/24/2012
Entry Details Article
PubMed
TargetHistone deacetylase 4(Human)
University of Wisconsin-Milwaukee

Curated by ChEMBL
LigandPNGBDBM50354088(CHEMBL1836142)
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of recombinant human HDAC4 using Boc-L-Lys(epsilon-trifluoroacetyl)-AMC as substrate by two-step fluorogenic assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/24/2012
Entry Details Article
PubMed
TargetHistone deacetylase 6(Human)
University of Wisconsin-Milwaukee

Curated by ChEMBL
LigandPNGBDBM50354088(CHEMBL1836142)
Affinity DataIC50: 9.90E+3nMAssay Description:Inhibition of recombinant human HDAC6 using Boc-L-Lys(epsilon-acetyl)-AMC as substrate by two-step fluorogenic assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/24/2012
Entry Details Article
PubMed
TargetHistone deacetylase 6(Mouse)
Tohoku Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50354088(CHEMBL1836142)
Affinity DataIC50: 992nMAssay Description:Inhibition of mouse HDAC6 expressed in human 293T cells using Ac-KGLGK(Ac)-MCA as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetHistone deacetylase 4(Human)
University of Wisconsin-Milwaukee

Curated by ChEMBL
LigandPNGBDBM50354088(CHEMBL1836142)
Affinity DataIC50: 3.72E+4nMAssay Description:Inhibition of human recombinant HDAC4 after 1 hr by luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/2/2020
Entry Details Article
PubMed
TargetHistone deacetylase 6(Human)
University of Wisconsin-Milwaukee

Curated by ChEMBL
LigandPNGBDBM50354088(CHEMBL1836142)
Affinity DataIC50: 830nMAssay Description:Inhibition of human recombinant HDAC6 after 1 hr by luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/2/2020
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
University of Wisconsin-Milwaukee

Curated by ChEMBL
LigandPNGBDBM50354088(CHEMBL1836142)
Affinity DataIC50: 0.280nMAssay Description:Inhibition of human recombinant HDAC1 after 1 hr by luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/2/2020
Entry Details Article
PubMed