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Found 21 Enz. Inhib. hit(s) with all data for entry = 9833
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492604(US10980781, Compound 14 | US11617738, Compound 14)
Affinity DataIC50:  530nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492588(6-Amino-4-(4-hydroxy-3-(trifluoromethyl)phenyl)-3-...)
Affinity DataIC50:  750nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492603(6-Amino-4-(3-iodo-4-methoxyphenyl)-3-(1-methyl-1H-...)
Affinity DataIC50:  1.31E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492589(6-Amino-4-(5-isopropyl-4-methoxy-2-methylphenyl)-3...)
Affinity DataIC50:  1.40E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492592(6-Amino-4-(3-iodo-4-methoxyphenyl)-3-(thiophen-2-y...)
Affinity DataIC50:  1.80E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492602(6-Amino-4-(3-bromo-4-methoxyphenyl)-3-(1-methyl-1H...)
Affinity DataIC50:  1.91E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492584(6-Amino-4-(3-bromo-4-methoxyphenyl)-3-(thiophen-2-...)
Affinity DataIC50:  3.70E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492597(6-Amino-4-(3-iodo-4-methoxyphenyl)-3-(pyridin-2-yl...)
Affinity DataIC50:  4.40E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492586(6-Amino-4-(3-bromo-4-(prop-2-yn-1-yloxy)phenyl)-3-...)
Affinity DataIC50:  4.50E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492592(6-Amino-4-(3-iodo-4-methoxyphenyl)-3-(thiophen-2-y...)
Affinity DataIC50:  5.60E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492590(6-Amino-4-(3-fluoro-4-methoxyphenyl)-3-(thiophen-2...)
Affinity DataIC50:  7.00E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492591(6-Amino-4-(3-chloro-4-methoxyphenyl)-3-(thiophen-2...)
Affinity DataIC50:  7.00E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492600(6-Amino-4-(3-bromo-4-methoxyphenyl)-3-(4-chlorophe...)
Affinity DataIC50:  7.50E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492599(6-Amino-4-(3-iodo-4-methoxyphenyl)-3-(pyridin-3-yl...)
Affinity DataIC50:  7.70E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492596(6-Amino-4-(3-iodo-4-methoxyphenyl)-3-(thiophen-3-y...)
Affinity DataIC50:  7.90E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492584(6-Amino-4-(3-bromo-4-methoxyphenyl)-3-(thiophen-2-...)
Affinity DataIC50:  8.10E+3nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492588(6-Amino-4-(4-hydroxy-3-(trifluoromethyl)phenyl)-3-...)
Affinity DataIC50:  1.10E+4nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492587(6-Amino-4-(2,3-dihydrobenzofuran-5-yl)-3-(thiophen...)
Affinity DataIC50:  1.30E+4nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492601(6-Amino-3-(4-chlorophenyl)-4-(3-iodo-4-methoxyphen...)
Affinity DataIC50:  1.50E+4nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492598(6-Amino-4-(3-bromo-4-methoxyphenyl)-3-(pyridin-3-y...)
Affinity DataIC50:  2.40E+4nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Purdue Research Foundation

US Patent
LigandPNGBDBM492585(US10980781, Compound 6g | US10980781, Entry 7 | US...)
Affinity DataIC50:  3.30E+4nMAssay Description:The lyophilized compounds were re-suspended in 100% DMSO to a stock concentration of 10 mM and stored at −20° C. Where Ratesample is the initia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent