Compile Data Set for Download or QSAR
maximum 50k data
Found 63 with Last Name = 'tang' and Initial = 'sp'
TargetProstaglandin E2 receptor EP1 subtype(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50160917(3-(3-(2-(benzyloxy)-5-chlorophenyl)thiophen-2-yl)b...)
Affinity DataKi:  0.300nMAssay Description:Antagonist activity against PGE2 activated EP1 receptor assessed as ability to inhibit intracellular calcium mobilisation by FLIPRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin E2 receptor EP1 subtype(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50160917(3-(3-(2-(benzyloxy)-5-chlorophenyl)thiophen-2-yl)b...)
Affinity DataIC50:  5nMAssay Description:Displacement of [3H]PGE2 from human EP1 receptor expressed in CHO-K1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418862(CHEMBL1801455)
Affinity DataIC50:  31.6nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50348620(CHEMBL1801364 | CHEMBL1801372)
Affinity DataIC50:  39.8nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418877(CHEMBL1801456)
Affinity DataIC50:  39.8nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50415892(CHEMBL1094411)
Affinity DataIC50:  39.8nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418870(CHEMBL1801366)
Affinity DataIC50:  50.1nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418863(CHEMBL1801367)
Affinity DataIC50:  50.1nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418861(CHEMBL1801457)
Affinity DataIC50:  50.1nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418865(CHEMBL1801368)
Affinity DataIC50:  50.1nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418869(CHEMBL1801369)
Affinity DataIC50:  50.1nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418871(CHEMBL1801462)
Affinity DataIC50:  63.1nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418876(CHEMBL1801458)
Affinity DataIC50:  63.1nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418867(CHEMBL1801370)
Affinity DataIC50:  100nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418872(CHEMBL1801454)
Affinity DataIC50:  100nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418873(CHEMBL1801365)
Affinity DataIC50:  100nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418864(CHEMBL1801459)
Affinity DataIC50:  126nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418873(CHEMBL1801365)
Affinity DataIC50:  158nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418872(CHEMBL1801454)
Affinity DataIC50:  158nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418866(CHEMBL1801371)
Affinity DataIC50:  158nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418874(CHEMBL1801460)
Affinity DataIC50:  200nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418874(CHEMBL1801460)
Affinity DataIC50:  251nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50415892(CHEMBL1094411)
Affinity DataIC50:  251nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50348620(CHEMBL1801364 | CHEMBL1801372)
Affinity DataIC50:  316nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418875(CHEMBL1801461)
Affinity DataIC50:  398nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418877(CHEMBL1801456)
Affinity DataIC50:  398nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418869(CHEMBL1801369)
Affinity DataIC50:  501nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418875(CHEMBL1801461)
Affinity DataIC50:  501nMAssay Description:Antagonist activity at human recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418861(CHEMBL1801457)
Affinity DataIC50:  631nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418862(CHEMBL1801455)
Affinity DataIC50:  631nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418863(CHEMBL1801367)
Affinity DataIC50:  631nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418871(CHEMBL1801462)
Affinity DataIC50:  631nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418864(CHEMBL1801459)
Affinity DataIC50:  1.00E+3nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50183189(3-(3-(2-(benzyloxy)-5-chlorophenyl)pyridin-4-yl)be...)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibition of CYP450 3A4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418870(CHEMBL1801366)
Affinity DataIC50:  1.58E+3nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50183187(3-(5-(2-(benzyloxy)-5-chlorophenyl)-1H-imidazol-1-...)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibition of CYP450 2C9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418865(CHEMBL1801368)
Affinity DataIC50:  3.16E+3nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50183182(2''-benzyloxy-5''-chloro-[1,1';2',1'']terphenyl-3-...)
Affinity DataIC50:  3.90E+3nMAssay Description:Inhibition of CYP450 2C9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50187023(3-(2-(2-(4-fluorobenzyloxy)-5-bromophenyl)-5-methy...)
Affinity DataIC50:  3.90E+3nMAssay Description:Inhibition of CYP450 2C9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418866(CHEMBL1801371)
Affinity DataIC50:  3.98E+3nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50183189(3-(3-(2-(benzyloxy)-5-chlorophenyl)pyridin-4-yl)be...)
Affinity DataIC50:  4.30E+3nMAssay Description:Inhibition of CYP450 2C9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50197894(2-(2-(2-(4-fluorobenzyloxy)-5-bromophenyl)cyclopen...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of human CYP2C9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50418867(CHEMBL1801370)
Affinity DataIC50:  5.01E+3nMAssay Description:Antagonist activity at rat recombinant P2X7 receptor expressed in HEK293 cells by ethidium bromide release assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50197895(6-(2-(2-(2,4-difluorobenzyloxy)-5-chlorophenyl)cyc...)
Affinity DataIC50:  5.40E+3nMAssay Description:Inhibition of human CYP2C9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50348620(CHEMBL1801364 | CHEMBL1801372)
Affinity DataIC50:  5.50E+3nMAssay Description:Inhibition of CYP3A4 using diethoxyflourescein as a substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50183188(3-(2-(2-(benzyloxy)-5-chlorophenyl)cyclopent-1-eny...)
Affinity DataIC50:  5.70E+3nMAssay Description:Inhibition of CYP450 2C9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50183185(3-(2-(2-(benzyloxy)-5-chlorophenyl)-5-methyl-1H-py...)
Affinity DataIC50:  6.50E+3nMAssay Description:Inhibition of CYP450 2C9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50183186(3-(2-(2-(benzyloxy)-5-bromophenyl)-5-methyl-1H-pyr...)
Affinity DataIC50:  6.80E+3nMAssay Description:Inhibition of CYP450 2C9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50183184(3-(2-(2-(benzyloxy)-5-chlorophenyl)-1H-pyrrol-1-yl...)
Affinity DataIC50:  7.30E+3nMAssay Description:Inhibition of CYP450 2C9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50197897(5-(2-(2-(4-fluorobenzyloxy)-5-chlorophenyl)cyclope...)
Affinity DataIC50:  9.00E+3nMAssay Description:Inhibition of human CYP2C9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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