Compile Data Set for Download or QSAR
maximum 50k data
Found 90 Enz. Inhib. hit(s) with all data for entry = 2358
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362853((R)-(8-methyl-3-(2- (trifluoromethyl)thiazol-4-yl)...)
Affinity DataKi:  13nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362853((R)-(8-methyl-3-(2- (trifluoromethyl)thiazol-4-yl)...)
Affinity DataKi:  13nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362854((R)-(3-chloro-4- fluorophenyl)(8-methyl-3-(2- (tri...)
Affinity DataKi:  14nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362854((R)-(3-chloro-4- fluorophenyl)(8-methyl-3-(2- (tri...)
Affinity DataKi:  14nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362851((R)-(3,4-difluorophenyl)(8- methyl-3-(2- (trifluor...)
Affinity DataKi:  20nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362851((R)-(3,4-difluorophenyl)(8- methyl-3-(2- (trifluor...)
Affinity DataKi:  20nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362856((R)-(4-chlorophenyl)(8- methyl-3-(2- (trifluoromet...)
Affinity DataKi:  21nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362856((R)-(4-chlorophenyl)(8- methyl-3-(2- (trifluoromet...)
Affinity DataKi:  21nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362855((R)-(4-chloro-3- fluorophenyl)(8-methyl-3-(2- (tri...)
Affinity DataKi:  22nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362841((R)-(4-fluorophenyl)(8- methyl-3-(2- (trifluoromet...)
Affinity DataKi:  22nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362855((R)-(4-chloro-3- fluorophenyl)(8-methyl-3-(2- (tri...)
Affinity DataKi:  22nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362841((R)-(4-fluorophenyl)(8- methyl-3-(2- (trifluoromet...)
Affinity DataKi:  22nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362849((R)-(3,4-dichlorophenyl)(8- methyl-3-(5-methylfura...)
Affinity DataKi:  27nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362849((R)-(3,4-dichlorophenyl)(8- methyl-3-(5-methylfura...)
Affinity DataKi:  27nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362850((R)-(8-methyl-3-(2- (trifluoromethyl)thiazol-4-yl)...)
Affinity DataKi:  29nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362850((R)-(8-methyl-3-(2- (trifluoromethyl)thiazol-4-yl)...)
Affinity DataKi:  29nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362845((R)-(8-methyl-3-(5- methylfuran-2-yl)-5,6-dihydro-...)
Affinity DataKi:  33nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362845((R)-(8-methyl-3-(5- methylfuran-2-yl)-5,6-dihydro-...)
Affinity DataKi:  33nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362848((R)-(4-chlorophenyl)(8- methyl-3-(5-methylfuran-2-...)
Affinity DataKi:  36nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362848((R)-(4-chlorophenyl)(8- methyl-3-(5-methylfuran-2-...)
Affinity DataKi:  36nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362847((R)-(4-chloro-3- fluorophenyl)(8-methyl-3-(5- meth...)
Affinity DataKi:  38nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362847((R)-(4-chloro-3- fluorophenyl)(8-methyl-3-(5- meth...)
Affinity DataKi:  38nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362852((R)-(8-methyl-3-(2- (trifluoromethyl)thiazol-4-yl)...)
Affinity DataKi:  40nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362852((R)-(8-methyl-3-(2- (trifluoromethyl)thiazol-4-yl)...)
Affinity DataKi:  40nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362843((R)-(3,4-difluorophenyl)(8- methyl-3-(5-methylfura...)
Affinity DataKi:  42nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362843((R)-(3,4-difluorophenyl)(8- methyl-3-(5-methylfura...)
Affinity DataKi:  42nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362846((R)-(3-chloro-4- fluorophenyl)(8-methyl-3-(5- meth...)
Affinity DataKi:  44nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362846((R)-(3-chloro-4- fluorophenyl)(8-methyl-3-(5- meth...)
Affinity DataKi:  44nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362839((R)-(4-fluorophenyl)(8- methyl-3-(5-methylfuran-2-...)
Affinity DataKi:  48nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362839((R)-(4-fluorophenyl)(8- methyl-3-(5-methylfuran-2-...)
Affinity DataKi:  48nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362842((R)-(8-methyl-3-(5- methylfuran-2-yl)-5,6-dihydro-...)
Affinity DataKi:  52nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362842((R)-(8-methyl-3-(5- methylfuran-2-yl)-5,6-dihydro-...)
Affinity DataKi:  52nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362844((R)-(8-methyl-3-(5- methylfuran-2-yl)-5,6-dihydro-...)
Affinity DataKi:  74nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362844((R)-(8-methyl-3-(5- methylfuran-2-yl)-5,6-dihydro-...)
Affinity DataKi:  74nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM50081280(CHEMBL3422005 | US9840508, Compound 2)
Affinity DataKi:  100nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetNeuromedin-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM50081280(CHEMBL3422005 | US9840508, Compound 2)
Affinity DataKi:  100nMAssay Description:The ability of compounds of the invention to inhibit the binding of the NK-3 receptor selective antagonist 3H-SB222200 was assessed by an in vitro ra...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetSubstance-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362854((R)-(3-chloro-4- fluorophenyl)(8-methyl-3-(2- (tri...)
Affinity DataKi:  1.50E+3nMAssay Description:The affinity of compounds of the invention for the NK-2 receptor was evaluated in CHO recombinant cells which express the human NK-2 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSubstance-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362853((R)-(8-methyl-3-(2- (trifluoromethyl)thiazol-4-yl)...)
Affinity DataKi:  3.50E+3nMAssay Description:The affinity of compounds of the invention for the NK-2 receptor was evaluated in CHO recombinant cells which express the human NK-2 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSubstance-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362849((R)-(3,4-dichlorophenyl)(8- methyl-3-(5-methylfura...)
Affinity DataKi:  4.20E+3nMAssay Description:The affinity of compounds of the invention for the NK-2 receptor was evaluated in CHO recombinant cells which express the human NK-2 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSubstance-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362850((R)-(8-methyl-3-(2- (trifluoromethyl)thiazol-4-yl)...)
Affinity DataKi:  4.70E+3nMAssay Description:The affinity of compounds of the invention for the NK-2 receptor was evaluated in CHO recombinant cells which express the human NK-2 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSubstance-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362855((R)-(4-chloro-3- fluorophenyl)(8-methyl-3-(2- (tri...)
Affinity DataKi:  5.20E+3nMAssay Description:The affinity of compounds of the invention for the NK-2 receptor was evaluated in CHO recombinant cells which express the human NK-2 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSubstance-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362856((R)-(4-chlorophenyl)(8- methyl-3-(2- (trifluoromet...)
Affinity DataKi:  5.90E+3nMAssay Description:The affinity of compounds of the invention for the NK-2 receptor was evaluated in CHO recombinant cells which express the human NK-2 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSubstance-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362841((R)-(4-fluorophenyl)(8- methyl-3-(2- (trifluoromet...)
Affinity DataKi:  6.60E+3nMAssay Description:The affinity of compounds of the invention for the NK-2 receptor was evaluated in CHO recombinant cells which express the human NK-2 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSubstance-P receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362849((R)-(3,4-dichlorophenyl)(8- methyl-3-(5-methylfura...)
Affinity DataKi:  6.90E+3nMAssay Description:The affinity of compounds of the invention for the NK-1 receptor was evaluated in CHO recombinant cells which express the human NK-1 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSubstance-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362851((R)-(3,4-difluorophenyl)(8- methyl-3-(2- (trifluor...)
Affinity DataKi:  7.00E+3nMAssay Description:The affinity of compounds of the invention for the NK-2 receptor was evaluated in CHO recombinant cells which express the human NK-2 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSubstance-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362846((R)-(3-chloro-4- fluorophenyl)(8-methyl-3-(5- meth...)
Affinity DataKi:  9.10E+3nMAssay Description:The affinity of compounds of the invention for the NK-2 receptor was evaluated in CHO recombinant cells which express the human NK-2 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSubstance-P receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362854((R)-(3-chloro-4- fluorophenyl)(8-methyl-3-(2- (tri...)
Affinity DataKi:  9.40E+3nMAssay Description:The affinity of compounds of the invention for the NK-1 receptor was evaluated in CHO recombinant cells which express the human NK-1 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSubstance-P receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362855((R)-(4-chloro-3- fluorophenyl)(8-methyl-3-(2- (tri...)
Affinity DataKi:  1.20E+4nMAssay Description:The affinity of compounds of the invention for the NK-1 receptor was evaluated in CHO recombinant cells which express the human NK-1 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSubstance-P receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362847((R)-(4-chloro-3- fluorophenyl)(8-methyl-3-(5- meth...)
Affinity DataKi:  1.30E+4nMAssay Description:The affinity of compounds of the invention for the NK-1 receptor was evaluated in CHO recombinant cells which express the human NK-1 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSubstance-K receptor(Homo sapiens (Human))
Oged

US Patent
LigandPNGBDBM362847((R)-(4-chloro-3- fluorophenyl)(8-methyl-3-(5- meth...)
Affinity DataKi:  1.40E+4nMAssay Description:The affinity of compounds of the invention for the NK-2 receptor was evaluated in CHO recombinant cells which express the human NK-2 receptor. Membra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
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