Compile Data Set for Download or QSAR
Report error Found 58 of ki for UniProtKB: P19971
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20079(5-chloro-6-[(2-iminopyrrolidin-1-yl)methyl]-1,2,3,...)
Affinity DataKi:  1.30nM ΔG°:  -12.6kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50121753(1-(5-Chloro-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin...)
Affinity DataKi:  5nMAssay Description:Binding affinity towards recombinant thymidine phosphorylase TPMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/7/2012
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20079(5-chloro-6-[(2-iminopyrrolidin-1-yl)methyl]-1,2,3,...)
Affinity DataKi:  17nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/28/2012
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50313094(5-fluoro-6-[(2-aminoimidazol-1-yl)methyl]uracil | ...)
Affinity DataKi:  17nMAssay Description:Inhibition of human thymidine phosphorylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50121753(1-(5-Chloro-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin...)
Affinity DataKi:  17nMAssay Description:Inhibitory activity against human thymidine phosphorylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/8/2012
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20079(5-chloro-6-[(2-iminopyrrolidin-1-yl)methyl]-1,2,3,...)
Affinity DataKi:  20nMAssay Description:Inhibitory activity against thymidine phosphorylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2012
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50531739(MA-1 | TPI (freebase) | Tipiracil)
Affinity DataKi:  20nMAssay Description:Competitive inhibition of thymidine phosphorylase (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/26/2021
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20079(5-chloro-6-[(2-iminopyrrolidin-1-yl)methyl]-1,2,3,...)
Affinity DataKi:  20nMAssay Description:Inhibition of human recombinant thymidine phosphorylase by [3H]thymidine incorporation assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20061(6-chloro-5-(cyclopent-1-en-1-yl)-1,2,3,4-tetrahydr...)
Affinity DataKi:  200nM ΔG°:  -9.50kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50310199((1-fluoro-3-(5-methyl-2,4-dioxo-3,4-dihydropyrimid...)
Affinity DataKi:  236nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/28/2012
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50310200((1-hydroxy-3-(5-methyl-2,4-dioxo-3,4-dihydropyrimi...)
Affinity DataKi:  236nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/28/2012
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50310201((1-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-...)
Affinity DataKi:  236nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/28/2012
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50310202((2-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-...)
Affinity DataKi:  236nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/28/2012
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50201010(((2R,3aR,4R,6R,6aR)-4-(hydroxymethyl)-6-(5-methyl-...)
Affinity DataKi:  236nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/28/2012
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50310203(8-(5-bromo-3-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydro...)
Affinity DataKi:  236nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/28/2012
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50201010(((2R,3aR,4R,6R,6aR)-4-(hydroxymethyl)-6-(5-methyl-...)
Affinity DataKi:  236nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20069(6-chloro-5-(thiophen-2-yl)-1,2,3,4-tetrahydropyrim...)
Affinity DataKi:  280nM ΔG°:  -9.29kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20065(6-chloro-5-phenyl-1,2,3,4-tetrahydropyrimidine-2,4...)
Affinity DataKi:  400nM ΔG°:  -9.07kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20073(6-chloro-5-[(1E)-pent-1-en-1-yl]-1,2,3,4-tetrahydr...)
Affinity DataKi:  410nM ΔG°:  -9.06kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20062(6-chloro-5-(cyclohex-1-en-1-yl)-1,2,3,4-tetrahydro...)
Affinity DataKi:  420nM ΔG°:  -9.04kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20064(6-chloro-5-[(2E)-pent-2-en-3-yl]-1,2,3,4-tetrahydr...)
Affinity DataKi:  490nM ΔG°:  -8.95kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20075(6-fluoro-5-phenyl-1,2,3,4-tetrahydropyrimidine-2,4...)
Affinity DataKi:  500nM ΔG°:  -8.94kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20072(5-[(1E)-but-1-en-1-yl]-6-chloro-1,2,3,4-tetrahydro...)
Affinity DataKi:  630nM ΔG°:  -8.79kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20068(6-chloro-5-(4-fluorophenyl)-1,2,3,4-tetrahydropyri...)
Affinity DataKi:  710nM ΔG°:  -8.72kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50117689(Thiophene-2-sulfonic acid [(E)-3-(3',4'-dichloro-b...)
Affinity DataKi:  770nMAssay Description:Inhibitory constant against Prostanoid TP receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20056(5-butyl-6-chloro-1,2,3,4-tetrahydropyrimidine-2,4-...)
Affinity DataKi:  1.03E+3nM ΔG°:  -8.49kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50201013(((2S,3aR,4S,6R,6aR)-4-(hydroxymethyl)-6-(5-methyl-...)
Affinity DataKi:  1.05E+3nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20059(6-chloro-5-heptyl-1,2,3,4-tetrahydropyrimidine-2,4...)
Affinity DataKi:  1.06E+3nM ΔG°:  -8.47kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20071(6-chloro-5-[(1E)-prop-1-en-1-yl]-1,2,3,4-tetrahydr...)
Affinity DataKi:  1.17E+3nM ΔG°:  -8.41kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20076(6-bromo-5-phenyl-1,2,3,4-tetrahydropyrimidine-2,4-...)
Affinity DataKi:  1.21E+3nM ΔG°:  -8.39kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50004462(CHEMBL3233329)
Affinity DataKi:  1.65E+3nMAssay Description:Mixed-type inhibition of human recombinant thymidine phosphorylase expressed in Escherichia coli assessed as conversion of thymidide to thymine by Li...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/7/2015
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20066(6-chloro-5-(3,5-dimethylphenyl)-1,2,3,4-tetrahydro...)
Affinity DataKi:  1.74E+3nM ΔG°:  -8.17kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50004460(CHEMBL3233327)
Affinity DataKi:  1.77E+3nMAssay Description:Mixed-type inhibition of human recombinant thymidine phosphorylase expressed in Escherichia coli assessed as conversion of thymidide to thymine by Li...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/7/2015
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20058(6-chloro-5-hexyl-1,2,3,4-tetrahydropyrimidine-2,4-...)
Affinity DataKi:  1.83E+3nM ΔG°:  -8.14kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50122770(6-amino-5-bromo-1,2,3,4-tetrahydropyrimidine-2,4-d...)
Affinity DataKi:  2.60E+3nMAssay Description:Inhibitory activity against Escherichia coli thymidine phosphorylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/8/2012
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20070(6-chloro-5-(pyridin-3-yl)-1,2,3,4-tetrahydropyrimi...)
Affinity DataKi:  3.01E+3nM ΔG°:  -7.83kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20063(6-chloro-5-(prop-1-en-2-yl)-1,2,3,4-tetrahydropyri...)
Affinity DataKi:  3.34E+3nM ΔG°:  -7.77kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20057(6-chloro-5-pentyl-1,2,3,4-tetrahydropyrimidine-2,4...)
Affinity DataKi:  3.67E+3nM ΔG°:  -7.71kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20067(6-chloro-5-(naphthalen-1-yl)-1,2,3,4-tetrahydropyr...)
Affinity DataKi:  4.59E+3nM ΔG°:  -7.57kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20060(5-benzyl-6-chloro-1,2,3,4-tetrahydropyrimidine-2,4...)
Affinity DataKi:  4.65E+3nM ΔG°:  -7.56kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20055(6-chloro-5-propyl-1,2,3,4-tetrahydropyrimidine-2,4...)
Affinity DataKi:  5.81E+3nM ΔG°:  -7.43kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50201015(((2R,3aR,4R,6R,6aS)-6-(hydroxymethyl)-4-(5-methyl-...)
Affinity DataKi:  8.03E+3nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50439105(CHEMBL2418061)
Affinity DataKi:  1.96E+4nMAssay Description:Mixed inhibition of human recombinant thymidine phosphorylase expressed in Escherichia coli using thymidine as substrate by Lineweaver-Burk plot anal...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20077(5-phenyl-6-(pyrrolidin-1-yl)-1,2,3,4-tetrahydropyr...)
Affinity DataKi: >2.00E+4nM ΔG°: >-6.66kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20078(6-[(2-aminoethyl)amino]-5-phenyl-1,2,3,4-tetrahydr...)
Affinity DataKi: >2.00E+4nM ΔG°: >-6.66kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20054(6-chloro-5-ethyl-1,2,3,4-tetrahydropyrimidine-2,4-...)
Affinity DataKi: >2.00E+4nM ΔG°: >-6.66kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM20074(6-methyl-5-phenyl-1,2,3,4-tetrahydropyrimidine-2,4...)
Affinity DataKi: >2.00E+4nM ΔG°: >-6.66kcal/molepH: 6.4 T: 2°CAssay Description:The enzyme reaction was started by the addition of enzyme to the reaction mixture containing substrate and test compounds. The reaction was stopped b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50439106(CHEMBL2418074)
Affinity DataKi:  2.01E+4nMAssay Description:Mixed inhibition of human recombinant thymidine phosphorylase expressed in Escherichia coli using thymidine as substrate by Lineweaver-Burk plot anal...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50201012(((2R,3aR,4S,6R,6aR)-4-(hydroxymethyl)-6-(5-methyl-...)
Affinity DataKi:  3.34E+4nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidine phosphorylase(Human)
Gilead Sciences

LigandPNGBDBM50201011(2-((2R,3aR,4R,6R,6aR)-4-(hydroxymethyl)-6-(5-methy...)
Affinity DataKi:  4.35E+4nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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