BDBM50304368 CHEMBL595582::N-(4-(N-1,3,4-thiadiazol-2-ylsulfamoyl)phenyl)decanamide::US9320734, 101

SMILES CCCCCCCCCC(=O)Nc1ccc(cc1)S(=O)(=O)Nc1nncs1

InChI Key InChIKey=YWVBYQMBZAUQKJ-UHFFFAOYSA-N

Data  2 KI  3 IC50  3 Kd

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50304368   

TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50304368(CHEMBL595582 | N-(4-(N-1,3,4-thiadiazol-2-ylsulfam...)
Affinity DataKi:  2.18E+4nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase(Mus musculus)
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50304368(CHEMBL595582 | N-(4-(N-1,3,4-thiadiazol-2-ylsulfam...)
Affinity DataKi:  2.20E+4nMAssay Description:Displacement of biotinylated phosphatidylinositol-3,4,5-phosphate from mouse AKT1 PH domain by surface plasmon resonance competitive binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50304368(CHEMBL595582 | N-(4-(N-1,3,4-thiadiazol-2-ylsulfam...)
Affinity DataIC50:  1.50E+4nMAssay Description:Inhibition of AKT was measured by Western blots using specific antibodies against phospho-Ser473-AKT in HT-29 lung cancer cells. Inhibition of the ph...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
The University Of Texas

Curated by ChEMBL
LigandPNGBDBM50304368(CHEMBL595582 | N-(4-(N-1,3,4-thiadiazol-2-ylsulfam...)
Affinity DataKd:  1.96E+4nMAssay Description:Inhibition of pleckstrin homology domain of AKT by surface plasmon resonance spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
The University Of Texas

Curated by ChEMBL
LigandPNGBDBM50304368(CHEMBL595582 | N-(4-(N-1,3,4-thiadiazol-2-ylsulfam...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of Akt phosphorylation in human BxPC3 cells by Western blottingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50304368(CHEMBL595582 | N-(4-(N-1,3,4-thiadiazol-2-ylsulfam...)
Affinity DataKd:  1.96E+4nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50304368(CHEMBL595582 | N-(4-(N-1,3,4-thiadiazol-2-ylsulfam...)
Affinity DataKd:  1.02E+4nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50304368(CHEMBL595582 | N-(4-(N-1,3,4-thiadiazol-2-ylsulfam...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of AKT was measured by Western blots using specific antibodies against phospho-Ser473-AKT in HT-29 lung cancer cells. Inhibition of the ph...More data for this Ligand-Target Pair
In DepthDetails US Patent