Compile Data Set for Download or QSAR
Found 96 with Last Name = 'brotherton-pleiss' and Initial = 'ce'
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
HOFFMANN-LA INC.

US Patent
LigandPNGBDBM205093(US9556147, 2)copy SMILEScopy InChI
Affinity DataIC50: 0.820nMpH: 7.2Assay Description:The assay is a capture of radioactive 33P phosphorylated product through filtration. The interactions of BTK, biotinylated SH2 peptide substrate (Src...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HX1FP9US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
HOFFMANN-LA INC.

US Patent
LigandPNGBDBM205094(US9556147, 3)copy SMILEScopy InChI
Affinity DataIC50: 0.910nMpH: 7.2Assay Description:The assay is a capture of radioactive 33P phosphorylated product through filtration. The interactions of BTK, biotinylated SH2 peptide substrate (Src...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
HOFFMANN-LA INC.

US Patent
LigandPNGBDBM205082(US9556147, 1)copy SMILEScopy InChI
Affinity DataIC50: 0.920nMpH: 7.2Assay Description:The assay is a capture of radioactive 33P phosphorylated product through filtration. The interactions of BTK, biotinylated SH2 peptide substrate (Src...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
HOFFMANN-LA INC.

US Patent
LigandPNGBDBM205095(US9556147, 4)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMpH: 7.2Assay Description:The assay is a capture of radioactive 33P phosphorylated product through filtration. The interactions of BTK, biotinylated SH2 peptide substrate (Src...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HX1FP9US Patent
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM291171(US9580411, Example 86)copy SMILEScopy InChI
Affinity DataIC50: 9nMT: 2°CAssay Description:IC50s (effective concentration) of compounds on the human TRPA1 channel were determined using a Hamamatsu FDSS fluorescence plate reader. CHO cells e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25T3NJMUS Patent
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM291170(2-[N-(Propan-2-yl)(4-fluorobenzene)sulfonamido]-N-...)copy SMILEScopy InChI
Affinity DataIC50: 13nMT: 2°CAssay Description:IC50s (effective concentration) of compounds on the human TRPA1 channel were determined using a Hamamatsu FDSS fluorescence plate reader. CHO cells e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25T3NJMUS Patent
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM291169(1-(4-Fluoro-N-isopropylphenylsulfonamido)-N-((6-(6...)copy SMILEScopy InChI
Affinity DataIC50: 29nMT: 2°CAssay Description:IC50s (effective concentration) of compounds on the human TRPA1 channel were determined using a Hamamatsu FDSS fluorescence plate reader. CHO cells e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25T3NJMUS Patent
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415550(CHEMBL599760 | Ro-85)copy SMILEScopy InChI
Affinity DataIC50: 31.6nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM291163(US9580411, Example 79-(R) | US9580411, Example 79-...)copy SMILEScopy InChI
Affinity DataIC50: 38nMT: 2°CAssay Description:IC50s (effective concentration) of compounds on the human TRPA1 channel were determined using a Hamamatsu FDSS fluorescence plate reader. CHO cells e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25T3NJMUS Patent
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415553(CHEMBL605130)copy SMILEScopy InChI
Affinity DataIC50: 39.8nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415601(CHEMBL598103)copy SMILEScopy InChI
Affinity DataIC50: 39.8nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415574(CHEMBL597486)copy SMILEScopy InChI
Affinity DataIC50: 50.1nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM291163(US9580411, Example 79-(R) | US9580411, Example 79-...)copy SMILEScopy InChI
Affinity DataIC50: 55nMT: 2°CAssay Description:IC50s (effective concentration) of compounds on the human TRPA1 channel were determined using a Hamamatsu FDSS fluorescence plate reader. CHO cells e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25T3NJMUS Patent
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM291168(2,2-Dideuterio-2-(4-fluoro-N-isopropylphenylsulfon...)copy SMILEScopy InChI
Affinity DataIC50: 58nMT: 2°CAssay Description:IC50s (effective concentration) of compounds on the human TRPA1 channel were determined using a Hamamatsu FDSS fluorescence plate reader. CHO cells e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25T3NJMUS Patent
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415599(CHEMBL604740)copy SMILEScopy InChI
Affinity DataIC50: 63.1nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415550(CHEMBL599760 | Ro-85)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415564(CHEMBL598728)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415575(CHEMBL597485)copy SMILEScopy InChI
Affinity DataIC50: 126nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM234880(US9359337, 11)copy SMILEScopy InChI
Affinity DataIC50: 151nMT: 2°CAssay Description:Compound plates were resuspended with 100 ul of HBSS/20 mM HEPES/0.005% BSA buffer (Compound Buffer): column 1A-H: buffer/DMSO (bk); column 2A-H: AP-...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q81BZZUS Patent
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM234877(US9359337, 8)copy SMILEScopy InChI
Affinity DataIC50: 193nMT: 2°CAssay Description:Compound plates were resuspended with 100 ul of HBSS/20 mM HEPES/0.005% BSA buffer (Compound Buffer): column 1A-H: buffer/DMSO (bk); column 2A-H: AP-...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q81BZZUS Patent
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415583(CHEMBL597110)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM234878(US9359337, 9)copy SMILEScopy InChI
Affinity DataIC50: 226nMT: 2°CAssay Description:Compound plates were resuspended with 100 ul of HBSS/20 mM HEPES/0.005% BSA buffer (Compound Buffer): column 1A-H: buffer/DMSO (bk); column 2A-H: AP-...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q81BZZUS Patent
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM234871(US9359337, 2)copy SMILEScopy InChI
Affinity DataIC50: 233nMT: 2°CAssay Description:Compound plates were resuspended with 100 ul of HBSS/20 mM HEPES/0.005% BSA buffer (Compound Buffer): column 1A-H: buffer/DMSO (bk); column 2A-H: AP-...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q81BZZUS Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
HOFFMANN-LA INC.

US Patent
LigandPNGBDBM205097(US9556147, 6)copy SMILEScopy InChI
Affinity DataIC50: 235nMpH: 7.2Assay Description:The assay is a capture of radioactive 33P phosphorylated product through filtration. The interactions of BTK, biotinylated SH2 peptide substrate (Src...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HX1FP9US Patent
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM291165(2-(4-Fluoro-N-isopropylphenylsulfonamido)-N-((6-(4...)copy SMILEScopy InChI
Affinity DataIC50: 251nMT: 2°CAssay Description:IC50s (effective concentration) of compounds on the human TRPA1 channel were determined using a Hamamatsu FDSS fluorescence plate reader. CHO cells e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25T3NJMUS Patent
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415563(CHEMBL605325)copy SMILEScopy InChI
Affinity DataIC50: 251nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM234874(US9359337, 5)copy SMILEScopy InChI
Affinity DataIC50: 307nMT: 2°CAssay Description:Compound plates were resuspended with 100 ul of HBSS/20 mM HEPES/0.005% BSA buffer (Compound Buffer): column 1A-H: buffer/DMSO (bk); column 2A-H: AP-...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q81BZZUS Patent
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM234881(US9359337, 12)copy SMILEScopy InChI
Affinity DataIC50: 385nMT: 2°CAssay Description:Compound plates were resuspended with 100 ul of HBSS/20 mM HEPES/0.005% BSA buffer (Compound Buffer): column 1A-H: buffer/DMSO (bk); column 2A-H: AP-...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q81BZZUS Patent
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415578(CHEMBL603453)copy SMILEScopy InChI
Affinity DataIC50: 398nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415566(CHEMBL604571)copy SMILEScopy InChI
Affinity DataIC50: 398nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(Homo sapiens (Human))
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415550(CHEMBL599760 | Ro-85)copy SMILEScopy InChI
Affinity DataIC50: 398nMAssay Description:Antagonist activity at human P2X3 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
HOFFMANN-LA INC.

US Patent
LigandPNGBDBM205096(US9556147, 5)copy SMILEScopy InChI
Affinity DataIC50: 414nMpH: 7.2Assay Description:The assay is a capture of radioactive 33P phosphorylated product through filtration. The interactions of BTK, biotinylated SH2 peptide substrate (Src...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HX1FP9US Patent
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM234873(US9359337, 4)copy SMILEScopy InChI
Affinity DataIC50: 425nMT: 2°CAssay Description:Compound plates were resuspended with 100 ul of HBSS/20 mM HEPES/0.005% BSA buffer (Compound Buffer): column 1A-H: buffer/DMSO (bk); column 2A-H: AP-...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q81BZZUS Patent
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM234870(US9359337, 1)copy SMILEScopy InChI
Affinity DataIC50: 494nMT: 2°CAssay Description:Compound plates were resuspended with 100 ul of HBSS/20 mM HEPES/0.005% BSA buffer (Compound Buffer): column 1A-H: buffer/DMSO (bk); column 2A-H: AP-...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q81BZZUS Patent
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415571(CHEMBL598498)copy SMILEScopy InChI
Affinity DataIC50: 501nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415576(CHEMBL597285)copy SMILEScopy InChI
Affinity DataIC50: 501nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415577(CHEMBL597480)copy SMILEScopy InChI
Affinity DataIC50: 501nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415593(CHEMBL599348)copy SMILEScopy InChI
Affinity DataIC50: 501nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM234875(US9359337, 6)copy SMILEScopy InChI
Affinity DataIC50: 504nMT: 2°CAssay Description:Compound plates were resuspended with 100 ul of HBSS/20 mM HEPES/0.005% BSA buffer (Compound Buffer): column 1A-H: buffer/DMSO (bk); column 2A-H: AP-...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q81BZZUS Patent
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415586(CHEMBL603254)copy SMILEScopy InChI
Affinity DataIC50: 631nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415569(CHEMBL605156)copy SMILEScopy InChI
Affinity DataIC50: 631nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM234872(US9359337, 3)copy SMILEScopy InChI
Affinity DataIC50: 634nMT: 2°CAssay Description:Compound plates were resuspended with 100 ul of HBSS/20 mM HEPES/0.005% BSA buffer (Compound Buffer): column 1A-H: buffer/DMSO (bk); column 2A-H: AP-...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q81BZZUS Patent
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM291161(2-(4-fluoro-N-isopropylphenylsulfonamido)-N-(3-(py...)copy SMILEScopy InChI
Affinity DataIC50: 883nMT: 2°CAssay Description:IC50s (effective concentration) of compounds on the human TRPA1 channel were determined using a Hamamatsu FDSS fluorescence plate reader. CHO cells e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25T3NJMUS Patent
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Hoffmann-La Roche Inc.

US Patent
LigandPNGBDBM291162(N-(3-cyclopropylbenzyl)-2-(4-fluoro-N-isopropylphe...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMT: 2°CAssay Description:IC50s (effective concentration) of compounds on the human TRPA1 channel were determined using a Hamamatsu FDSS fluorescence plate reader. CHO cells e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25T3NJMUS Patent
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415596(CHEMBL596814)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415597(CHEMBL598729)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415587(CHEMBL598865)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415580(CHEMBL598471)copy SMILEScopy InChI
Affinity DataIC50: 1.26E+3nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415588(CHEMBL605322)copy SMILEScopy InChI
Affinity DataIC50: 1.26E+3nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
TargetP2X purinoceptor 3(RAT)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50415570(CHEMBL590972)copy SMILEScopy InChI
Affinity DataIC50: 1.26E+3nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2HCRPubMed
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