Compile Data Set for Download or QSAR
Found 268 with Last Name = 'kong' and Initial = 'nx'
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111887(1-{3-[4-((Z)-2-Iodo-propenyl)-phenyl]-8-aza-bicycl...)copy SMILEScopy InChI
Affinity DataKi:  0.130nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111894(1-{3-[4-((E)-2-Iodo-propenyl)-phenyl]-8-aza-bicycl...)copy SMILEScopy InChI
Affinity DataKi:  0.570nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111881(1-{3-[4-((E)-2-Iodo-vinyl)-phenyl]-8-aza-bicyclo[3...)copy SMILEScopy InChI
Affinity DataKi:  0.620nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111889(1-[3-(3-Chloro-4-iodo-phenyl)-8-methyl-8-aza-bicyc...)copy SMILEScopy InChI
Affinity DataKi:  1.10nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111893(1-[3-(3-Chloro-4-iodo-phenyl)-8-aza-bicyclo[3.2.1]...)copy SMILEScopy InChI
Affinity DataKi:  1.10nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111891(1-[3-(4-Iodo-phenyl)-8-methyl-8-aza-bicyclo[3.2.1]...)copy SMILEScopy InChI
Affinity DataKi:  1.90nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111883(1-[3-(4-Iodo-phenyl)-8-aza-bicyclo[3.2.1]oct-2-yl]...)copy SMILEScopy InChI
Affinity DataKi:  2.40nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111890(1-{8-((E)-3-Iodo-allyl)-3-[4-(1-methyl-1H-pyrrol-2...)copy SMILEScopy InChI
Affinity DataKi:  2.80nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111886(1-[3-(3-Fluoro-4-iodo-phenyl)-8-aza-bicyclo[3.2.1]...)copy SMILEScopy InChI
Affinity DataKi:  7.30nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111888(1-[3-(3-Fluoro-4-iodo-phenyl)-8-methyl-8-aza-bicyc...)copy SMILEScopy InChI
Affinity DataKi:  9.10nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111880(1-{8-((Z)-3-Iodo-allyl)-3-[4-(1-methyl-1H-pyrrol-2...)copy SMILEScopy InChI
Affinity DataKi:  13nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111885(1-[3-(3-Iodo-phenyl)-8-aza-bicyclo[3.2.1]oct-2-yl]...)copy SMILEScopy InChI
Affinity DataKi:  16nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111892(1-[3-(3-Iodo-phenyl)-8-methyl-8-aza-bicyclo[3.2.1]...)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111882((E)-5-Iodo-1-(8-methyl-3-p-tolyl-8-aza-bicyclo[3.2...)copy SMILEScopy InChI
Affinity DataKi:  51nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50451492(CHEMBL2112943)copy SMILEScopy InChI
Affinity DataKi: >1.10E+3nMAssay Description:Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111889(1-[3-(3-Chloro-4-iodo-phenyl)-8-methyl-8-aza-bicyc...)copy SMILEScopy InChI
Affinity DataIC50: 0.0770nMAssay Description:Tested for the ability to displace [125I]- RTI-55 binding in rat striatal membrane against dopamine transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111893(1-[3-(3-Chloro-4-iodo-phenyl)-8-aza-bicyclo[3.2.1]...)copy SMILEScopy InChI
Affinity DataIC50: 0.0850nMAssay Description:Tested for the ability to displace [125I]- RTI-55 binding in rat striatal membrane against dopamine transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111888(1-[3-(3-Fluoro-4-iodo-phenyl)-8-methyl-8-aza-bicyc...)copy SMILEScopy InChI
Affinity DataIC50: 0.380nMAssay Description:Tested for the ability to displace [125I]- RTI-55 binding in rat striatal membrane against dopamine transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111886(1-[3-(3-Fluoro-4-iodo-phenyl)-8-aza-bicyclo[3.2.1]...)copy SMILEScopy InChI
Affinity DataIC50: 1.10nMAssay Description:Tested for the ability to displace [125I]- RTI-55 binding in rat striatal membrane against dopamine transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111891(1-[3-(4-Iodo-phenyl)-8-methyl-8-aza-bicyclo[3.2.1]...)copy SMILEScopy InChI
Affinity DataIC50: 1.70nMAssay Description:Tested for the ability to displace [125I]- RTI-55 binding in rat striatal membrane against dopamine transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
State University of New York

Curated by ChEMBL
LigandPNGBDBM50111883(1-[3-(4-Iodo-phenyl)-8-aza-bicyclo[3.2.1]oct-2-yl]...)copy SMILEScopy InChI
Affinity DataIC50: 2.20nMAssay Description:Tested for the ability to displace [125I]- RTI-55 binding in rat striatal membrane against dopamine transporterMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M6515PubMed
TargetFibroblast growth factor receptor 3(Homo sapiens (Human))TBA
LigandPNGBDBM592211(US11572353, Compound 26)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
TargetFibroblast growth factor receptor 4(Homo sapiens (Human))TBA
LigandPNGBDBM592211(US11572353, Compound 26)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))TBA
LigandPNGBDBM592212(US11572353, Compound 27)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
TargetFibroblast growth factor receptor 3(Homo sapiens (Human))TBA
LigandPNGBDBM592213(US11572353, Compound 28)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))TBA
LigandPNGBDBM592214(US11572353, Compound 29)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
TargetFibroblast growth factor receptor 3(Homo sapiens (Human))TBA
LigandPNGBDBM592214(US11572353, Compound 29)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))TBA
LigandPNGBDBM592215(US11572353, Compound 30)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
TargetFibroblast growth factor receptor 3(Homo sapiens (Human))TBA
LigandPNGBDBM592215(US11572353, Compound 30)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))TBA
LigandPNGBDBM592216(US11572353, Compound 31)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
TargetFibroblast growth factor receptor 3(Homo sapiens (Human))TBA
LigandPNGBDBM592216(US11572353, Compound 31)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))TBA
LigandPNGBDBM592219(US11572353, Compound 34)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
TargetFibroblast growth factor receptor 3(Homo sapiens (Human))TBA
LigandPNGBDBM592219(US11572353, Compound 34)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436174(US10590109, Compound 1)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436187(US10590109, Compound 5)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436188(US10590109, Compound 6)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436189(US10590109, Compound 7)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436191(US10590109, Compound 9)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436192(US10590109, Compound 10)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436194(US10590109, Compound 12)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436196(US10590109, Compound 14)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436198(US10590109, Compound 16)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436200(US10590109, Compound 18 | US10590109, Compound 25)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436201(US10590109, Compound 19)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436197(US10590109, Compound 15 | US10590109, Compound 20)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436206(US10590109, Compound 24)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436200(US10590109, Compound 18 | US10590109, Compound 25)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 4 [460-802](Homo sapiens (Human))
Nanjing InnoCare Pharma Tech Co., Ltd.

US Patent
LigandPNGBDBM436208(US10590109, Compound 26)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:FGFR4:The in vitro activity of FGFR4 was determined by assaying the phosphorylation level of the substrate in the kinase reaction, by means of an HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J969D2US Patent
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))TBA
LigandPNGBDBM592193(US11572353, Compound 7)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))TBA
LigandPNGBDBM592193(US11572353, Compound 7)copy SMILES
Affinity DataIC50: 10nMAssay Description:The reaction buffer contains the following components: 5-fold diluted enzymatic buffer/kinase 5x(Cisbio, Cat No. 62EZBFDD)(its main component is 50nM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FF3X81US Patent
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