Compile Data Set for Download or QSAR
Found 553 with Last Name = 'hammond' and Initial = 'e'
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388329(CHEMBL2059500)copy SMILEScopy InChI
Affinity DataKi:  3.70nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388343(CHEMBL2059243)copy SMILEScopy InChI
Affinity DataKi:  5.5nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388341(CHEMBL2059241)copy SMILEScopy InChI
Affinity DataKi:  5.80nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388342(CHEMBL2059242)copy SMILEScopy InChI
Affinity DataKi:  6nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388331(CHEMBL2059499)copy SMILEScopy InChI
Affinity DataKi:  6.10nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388345(CHEMBL2059245)copy SMILEScopy InChI
Affinity DataKi:  6.40nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50378647(CHEMBL1627122 | PI-88)copy SMILEScopy InChI
Affinity DataKi:  7.90nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388332(CHEMBL2059498)copy SMILEScopy InChI
Affinity DataKi:  8.40nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388346(CHEMBL2059246)copy SMILEScopy InChI
Affinity DataKi:  8.5nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388335(CHEMBL2059503)copy SMILEScopy InChI
Affinity DataKi:  9.10nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388336(CHEMBL2059504)copy SMILEScopy InChI
Affinity DataKi:  9.10nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388330(CHEMBL2059247)copy SMILEScopy InChI
Affinity DataKi:  10.5nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388328(CHEMBL2059505)copy SMILEScopy InChI
Affinity DataKi:  11.3nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388334(CHEMBL2059501)copy SMILEScopy InChI
Affinity DataKi:  16nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388333(CHEMBL2059502)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388344(CHEMBL2059244)copy SMILEScopy InChI
Affinity DataKi:  22.3nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388340(CHEMBL2059510)copy SMILEScopy InChI
Affinity DataKi:  30nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50388338(CHEMBL2059508)copy SMILEScopy InChI
Affinity DataKi:  111nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G161WNPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50375292(CHEMBL407200)copy SMILEScopy InChI
Affinity DataKi:  200nMAssay Description:Inhibition of human platelet heparanase by competitive binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ918DPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50375290(CHEMBL279625)copy SMILEScopy InChI
Affinity DataKi:  240nMAssay Description:Inhibition of human platelet heparanase by competitive binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ918DPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50375291(CHEMBL439118)copy SMILEScopy InChI
Affinity DataKi:  280nMAssay Description:Inhibition of human platelet heparanase by competitive binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ918DPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50375287(CHEMBL260220)copy SMILEScopy InChI
Affinity DataKi:  2.23E+3nMAssay Description:Inhibition of human platelet heparanase by competitive binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ918DPubMed
TargetHeparanase(Homo sapiens (Human))
Progen Pharmaceuticals Limited

Curated by ChEMBL
LigandPNGBDBM50375287(CHEMBL260220)copy SMILEScopy InChI
Affinity DataKi:  6.83E+4nMAssay Description:Inhibition of human platelet heparanase by uncompetitive binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ918DPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265746(CHEMBL526507 | {4-Amino-3-[6-(4-methylpiperazinyl)...)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265774(4-Amino-3-benzimidazol-2-yl-5-(1-methyl(3-piperidy...)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265574(3-(1H-benzo[d]imidazol-2-yl)-4-(4-ethyl-1-methylpi...)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265773(4-Amino-3-benzimidazol-2-yl-5-(4-methylpiperazinyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265678(4-Amino-5-chloro-3-[6-(4-methylpiperazinyl)benzimi...)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265750(4-Amino-7-fluoro-3-[6-(4-methylpiperazinyl)benzimi...)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265745(4-Amino-6-(benzylamino)-3-(6-(4-methylpiperazin-1-...)copy SMILEScopy InChI
Affinity DataIC50: 0.600nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Biogen Inc.

Curated by ChEMBL
LigandPNGBDBM50074659((S)-2-[(S)-3-Carboxy-2-((S)-4-methyl-2-{2-[4-(3-o-...)copy SMILEScopy InChI
Affinity DataIC50: 0.600nMAssay Description:Inhibition of integrin alpha4-beta1 binding to VCAM-IgMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2P26XBFPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265679(4-Amino-5-methyl-3-[6-(4-methylpiperazinyl)benzimi...)copy SMILEScopy InChI
Affinity DataIC50: 0.700nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265641(4-Amino-3-{6-[(4-methylpiperazinyl)carbonyl]benzim...)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265613(3-(1H-benzo[d]imidazol-2-yl)-4-(piperidin-4-ylmeth...)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Biogen Inc.

Curated by ChEMBL
LigandPNGBDBM50074664((S)-N-[(S)-1-((S)-2-Carbamoyl-pyrrolidine-1-carbon...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of integrin alpha4-beta1 binding to VCAM-IgMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2P26XBFPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265738(4-Amino-6-fluoro-3-[6-(4-methylpiperazinyl)benzimi...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265773(4-Amino-3-benzimidazol-2-yl-5-(4-methylpiperazinyl...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human recombinant FGFR1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Biogen Inc.

Curated by ChEMBL
LigandPNGBDBM50074661((S)-1-{(S)-2-[(S)-3-Carboxy-2-((S)-4-methyl-2-{2-[...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of integrin alpha4-beta1 binding to VCAM-IgMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2P26XBFPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265676(CHEMBL495962 | N-(2-(4-Amino-2-oxo-1,2-dihydroquin...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Biogen Inc.

Curated by ChEMBL
LigandPNGBDBM50422305(CHEMBL1791268)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of integrin alpha4-beta1 binding to VCAM-IgMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2P26XBFPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265774(4-Amino-3-benzimidazol-2-yl-5-(1-methyl(3-piperidy...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human recombinant FGFR1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265675(4-Amino-3-(6-((4-methylpiperazin-1-yl)methyl)-1H-b...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50181320(4-Amino-3-[6-(4-methylpiperazinyl)benzimidazol-2-y...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265737(4-Amino-5-(methylamino)-3-(6-(4-methylpiperazin-1-...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of human recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265678(4-Amino-5-chloro-3-[6-(4-methylpiperazinyl)benzimi...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of human recombinant FGFR1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Biogen Inc.

Curated by ChEMBL
LigandPNGBDBM50074660((S)-2-[(S)-3-Carboxy-2-((S)-4-methyl-2-{2-[4-(3-ph...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of integrin alpha4-beta1 binding to VCAM-IgMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2P26XBFPubMed
TargetVascular endothelial growth factor receptor 3(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM25118((3Z)-4-amino-5-fluoro-3-[5-(4-methylpiperazino)-1,...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of VEGFR3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265750(4-Amino-7-fluoro-3-[6-(4-methylpiperazinyl)benzimi...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of human recombinant FGFR1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265679(4-Amino-5-methyl-3-[6-(4-methylpiperazinyl)benzimi...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of human recombinant FGFR1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50265676(CHEMBL495962 | N-(2-(4-Amino-2-oxo-1,2-dihydroquin...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of human recombinant FGFR1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TD9X7XPubMed
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