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Found 6686 with Last Name = 'srinivas' and Initial = 'v'
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052789(CHEMBL3318616)
Affinity DataKi:  0.100nMAssay Description:Irreversible inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052783(CHEMBL3318605)
Affinity DataKi:  0.160nMAssay Description:Irreversible inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052768(CHEMBL3318613)
Affinity DataKi:  0.160nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052771(CHEMBL3318617)
Affinity DataKi:  0.190nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052785(CHEMBL3318607)
Affinity DataKi:  0.290nMAssay Description:Irreversible inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052786(CHEMBL3318610)
Affinity DataKi:  0.360nMAssay Description:Irreversible inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052784(CHEMBL3318606)
Affinity DataKi:  0.470nMAssay Description:Irreversible inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052787(CHEMBL3318614)
Affinity DataKi:  9.20nMAssay Description:Irreversible inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052781(CHEMBL3318603)
Affinity DataKi:  9.80nMAssay Description:Irreversible inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052766(CHEMBL3318611)
Affinity DataKi:  10nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052769(CHEMBL3318608)
Affinity DataKi:  12nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50326165(CHEMBL1241315 | oxalylaminobenzoic acid)
Affinity DataKi:  18nMAssay Description:Inhibition of human recombinant PTP1B after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM13976(Aminobenzoic acid analog 5 | CHEMBL116605)
Affinity DataKi:  18nMAssay Description:Inhibition of PTP1BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052774(CHEMBL3318620)
Affinity DataKi:  42nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052762(CHEMBL3318593)
Affinity DataKi:  55nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM13976(Aminobenzoic acid analog 5 | CHEMBL116605)
Affinity DataKi:  65nMAssay Description:Inhibition of TCPTPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50326165(CHEMBL1241315 | oxalylaminobenzoic acid)
Affinity DataKi:  65nMAssay Description:Inhibition of human recombinant TCPTP after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052765(CHEMBL3318602)
Affinity DataKi:  75nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052760(CHEMBL3318590)
Affinity DataKi:  80nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052767(CHEMBL3318612)
Affinity DataKi:  100nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052782(CHEMBL3318604)
Affinity DataKi:  130nMAssay Description:Irreversible inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052770(CHEMBL3318609)
Affinity DataKi:  170nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052763(CHEMBL3318600)
Affinity DataKi:  180nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052777(CHEMBL3318623)
Affinity DataKi:  210nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052788(CHEMBL3318615)
Affinity DataKi:  210nMAssay Description:Irreversible inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052764(CHEMBL3318601)
Affinity DataKi:  250nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052772(CHEMBL3318618)
Affinity DataKi:  290nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052731(CHEMBL3318591)
Affinity DataKi:  340nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052773(CHEMBL3318619)
Affinity DataKi:  550nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052775(CHEMBL3318621)
Affinity DataKi:  710nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052791(CHEMBL3318588)
Affinity DataKi:  750nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052761(CHEMBL3318592)
Affinity DataKi:  850nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052790(CHEMBL3318589)
Affinity DataKi: >1.00E+3nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50296368(7-(biphenyl-4-yl)-4-oxo-4H-chromene-3-carbaldehyde...)
Affinity DataKi:  4.30E+3nMAssay Description:Inhibition of TCPTPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50296368(7-(biphenyl-4-yl)-4-oxo-4H-chromene-3-carbaldehyde...)
Affinity DataKi:  4.30E+3nMAssay Description:Inhibition of human recombinant PTP1B after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052776(CHEMBL3318622)
Affinity DataKi: >5.00E+3nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052778(CHEMBL3318624)
Affinity DataKi: >5.00E+3nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052779(CHEMBL3318625)
Affinity DataKi: >5.00E+3nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50052780(CHEMBL3318626)
Affinity DataKi: >5.00E+3nMAssay Description:Inhibition of recombinant rat FAAH preincubated for 3 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50133280(5-(3-(3-(3-hydroxy-2-(methoxycarbonyl)phenoxy)prop...)
Affinity DataKi:  5.70E+3nMAssay Description:Inhibition of human recombinant PTP1B after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50133280(5-(3-(3-(3-hydroxy-2-(methoxycarbonyl)phenoxy)prop...)
Affinity DataKi:  5.70E+3nMAssay Description:Inhibition of PTP1BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50296368(7-(biphenyl-4-yl)-4-oxo-4H-chromene-3-carbaldehyde...)
Affinity DataKi:  5.10E+4nMAssay Description:Inhibition of PTP1BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50296368(7-(biphenyl-4-yl)-4-oxo-4H-chromene-3-carbaldehyde...)
Affinity DataKi:  5.10E+4nMAssay Description:Inhibition of human recombinant TCPTP after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50133280(5-(3-(3-(3-hydroxy-2-(methoxycarbonyl)phenoxy)prop...)
Affinity DataKi:  2.02E+5nMAssay Description:Inhibition of human recombinant TCPTP after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50133280(5-(3-(3-(3-hydroxy-2-(methoxycarbonyl)phenoxy)prop...)
Affinity DataKi:  2.02E+5nMAssay Description:Inhibition of TCPTPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetToll-like receptor 7(Homo sapiens (Human))
Bristol-Myers Squibb

US Patent
LigandPNGBDBM516908(US11053244, Example 328 | US11053244, Example 329)
Affinity DataIC50:  0.0800nMAssay Description:HEK-Blue™-cells (Invivogen) overexpressing human TLR7, TLR8 or TLR9 receptors were used for screening inhibitors of these receptors using an inducibl...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetToll-like receptor 7(Homo sapiens (Human))
Bristol-Myers Squibb

US Patent
LigandPNGBDBM427894(US10544143, Example 328 | US10544143, Example 329 ...)
Affinity DataIC50:  0.0800nMAssay Description:HEK-Blue-cells (Invivogen) overexpressing human TLR7, TLR8 or TLR9 receptors were used for screening inhibitors of these receptors using an inducible...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetToll-like receptor 7(Homo sapiens (Human))
Bristol-Myers Squibb

US Patent
LigandPNGBDBM428633(US10544143, Example 1069 | US10544143, Example 107...)
Affinity DataIC50:  0.0900nMAssay Description:HEK-Blue™-cells (Invivogen) overexpressing human TLR7, TLR8 or TLR9 receptors were used for screening inhibitors of these receptors using an inducibl...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetToll-like receptor 7(Homo sapiens (Human))
Bristol-Myers Squibb

US Patent
LigandPNGBDBM428633(US10544143, Example 1069 | US10544143, Example 107...)
Affinity DataIC50:  0.0900nMAssay Description:HEK-Blue-cells (Invivogen) overexpressing human TLR7, TLR8 or TLR9 receptors were used for screening inhibitors of these receptors using an inducible...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetToll-like receptor 8(Homo sapiens (Human))
Bristol-Myers Squibb

US Patent
LigandPNGBDBM428533(US10544143, Example 969 | US10730877, Example 969 ...)
Affinity DataIC50:  0.120nMAssay Description:HEK-Blue-cells (Invivogen) overexpressing human TLR7, TLR8 or TLR9 receptors were used for screening inhibitors of these receptors using an inducible...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
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