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Acetaminophen (CID 1983) - Compound BioActivity Data
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BioActivity Outcomes:
Active(60)
 
 
Inactive(1235)
 
 
Inconclusive(98)
 
 
Unspecified(1838)
 
 
Top Targets:
p450(43)
 
 
 
 
 
7TM GPCR Srx(36)
 
 
 
NR LBD PPAR(34)
 
 
 
7TM GPCR Srsx(33)
 
 
 
NR LBD ER(27)
 
 
 
 
BioAssay Types:
Confirmatory(767)
 
 
 
 
 
Literature(437)
 
 
 
 
 
Screening(314)
 
 
 
Summary(72)
 
 
 
BioActivity Types:
Potency(720)
 
 
 
 
 
IC50(156)
 
 
 
 
 
Ki(17)
 
 
 
Kd(3)
 
 
AC50(2)
 
 
Data download

Chemical Probe    Active    Inactive    Inconclusive    Unspecified   

Total Bioassays: 2653    Data Row: 3231   Total Pages: 65   Display: Page     
Sort: [Click the result table header to sort]
#SubstanceActivityBioAssayTargetLinks
OutcomeTypeValue [μM]
1
[SID103178971]
Ki 4.1Inhibition of human carbonic anhydrase 12 catalytic domain by stopped-flow CO2 hydration assay [AID342484, Type: Literature]Carbonic anhydrase 12 [gi:5915866]
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2
[SID103178971]
Kd 5.79Binding affinity to human CYP1A1-heme complex [AID536418, Type: Literature]
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3
[SID103178971]
Ki 6.2Inhibition of human carbonic anhydrase 2 by stopped-flow CO2 hydrase assay [AID331292, Type: Literature]Carbonic anhydrase 2 [gi:115456]
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4
[SID103178971]
Ki 6.2Inhibition of human carbonic anhydrase 2 by stopped-flow CO2 hydration assay [AID342476, Type: Literature]Carbonic anhydrase 2 [gi:115456]
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5
[SID103178971]
Kd 6.64Binding affinity to rat CYP2B1-heme complex [AID536419, Type: Literature]
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6
[SID103178971]
Ki 7.1Inhibition of human carbonic anhydrase 3 by stopped-flow CO2 hydration assay [AID342477, Type: Literature]Carbonic anhydrase 3 [gi:134047703]
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7
[SID103178971]
Ki 9.1Inhibition of human carbonic anhydrase 7 by stopped-flow CO2 hydration assay [AID342482, Type: Literature]Carbonic anhydrase 7 [gi:1168744]
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8
[SID103178971]
Ki 9.23Inhibition of mouse recombinant carbonic anhydrase 15 by stopped-flow CO2 hydrase assay [AID331293, Type: Literature]Carbonic anhydrase 15 [gi:30580362]
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9
[SID103178971]
Ki 10Inhibition of human carbonic anhydrase 1 by stopped-flow CO2 hydration assay [AID342475, Type: Literature]Carbonic anhydrase 1 [gi:115449]
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10
[SID103178971]
Ki 10Inhibition of human carbonic anhydrase 1 by stopped-flow CO2 hydrase assay [AID331291, Type: Literature]Carbonic anhydrase 1 [gi:115449]
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11
[SID103178971]
Ki 10.6Inhibition of human carbonic anhydrase 14 by stopped-flow CO2 hydration assay [AID342485, Type: Literature]Carbonic anhydrase 14 [gi:8928036]
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12
[SID103178971]
Ki 11.4Inhibition of human carbonic anhydrase 4 by stopped-flow CO2 hydration assay [AID342478, Type: Literature]Carbonic anhydrase 4 [gi:115465]
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13
[SID56422763]
AC50_uM 14.53C. difficile toxins: Counterscreen in absence of substrate UDPG Measured in Biochemical System Using Plate Reader - 7074-02_Inhibitor_Dose_CherryPick_Activity [AID720650, Type: confirmatory]
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14
[SID103178971]
Kd 19.1Binding affinity to human CYP1A1 [AID536416, Type: Literature]Cytochrome P450 1A1 [gi:117139]
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15
[SID56422763]
AC50_uM 20.87C. difficile toxins: HTS for inhibitors of TcdB glycohydrolase activity Measured in Biochemical System Using Plate Reader - 7074-01_Inhibitor_Dose_CherryPick_Activity [AID720512, Type: confirmatory]toxin B [Clostridium difficile 630] [gi:126698238]
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16
[SID103178971]
IC50 28.38DRUGMATRIX: Lipoxygenase 15-LO enzyme inhibition (substrate: Linoleic acid) [AID625146, Type: other]Arachidonate 15-lipoxygenase [gi:126397]
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17
[SID103178971]
Ki 30.3Inhibition of mouse carbonic anhydrase 13 by stopped-flow CO2 hydration assay [AID342486, Type: Literature]Carbonic anhydrase 13 [gi:30580372]
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18
[SID103178971]
IC50 44Inhibition of FLAP [AID405531, Type: Literature]
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19
[SID103178971]
IC50 44Inhibition of LPS-stimulated PGE2 production in human whole blood [AID405541, Type: Literature]
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20
[SID144209128]
Potency-Replicate_1 71.0381qHTS assay for identifying genotoxic compounds that show differential cytotoxicity against isogenic chicken DT40 cell lines with known DNA damage response pathways - wild type cell line [AID743012, Type: confirmatory]
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21
[SID103178971]
FDA HLAED, liver enzyme composite activity [AID588214, Type: Literature]
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22
[SID103178971]
FDA HLAED, serum glutamic oxaloacetic transaminase (SGOT) increase [AID588216, Type: Literature]
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23
[SID103178971]
FDA HLAED, serum glutamic pyruvic transaminase (SGPT) increase [AID588217, Type: Literature]
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24
[SID103178971]
Binding affinity to His-6 tagged BRD2 expressed in Escherichia coli at 10 mM after 60 mins by fluorescence anisotropic analysis [AID646027, Type: Literature]
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25
[SID48413133]
DSSTox (CPDBAS) Carcinogenic Potency Database Summary Mouse Bioassay Results [AID1199, Type: other]
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26
[SID48413133]
DSSTox (CPDBAS) Carcinogenic Potency Database Summary MultiCellCall Results [AID1205, Type: other]
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27
[SID48413133]
DSSTox (CPDBAS) Carcinogenic Potency Database Summary Rat Bioassay Results [AID1208, Type: other]
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28
[SID48415047]
DSSTox (EPAFHM) EPA Fathead Minnow Acute Toxicity [AID1188, Type: other]
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29
[SID48415502]
DSSTox (FDAMDD) FDA Maximum (Recommended) Daily Dose Database [AID1195, Type: other]
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30
[SID48413133]
DSSTox (CPDBAS) Carcinogenic Potency Database Summary SingleCellCall Results [AID1189, Type: other]
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31
[SID56422763]
Aqueous Solubility from MLSMR Stock Solutions [AID1996, Type: other]
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32
[SID103178971]
Drug level in mouse brain at 50 mg/kg, po [AID263727, Type: Literature]
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33
[SID103178971]
Inhibition of human CYP1A2 assessed as ratio of IC50 in absence of NADPH to IC50 for presence of NADPH using ethoxyresorufin as substrate after 30 mins [AID678712, Type: Literature]Cytochrome P450 1A2 [gi:117144]
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34
[SID103178971]
Hepatotoxicity in CD1 mouse assessed as reduction in hepatic glutathione levels at 6 mmol/kg [AID304904, Type: Literature]
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35
[SID103178971]
Hepatotoxicity in CD1 mouse assessed as reduction in renal glutathione levels at 6 mmol/kg [AID304905, Type: Literature]
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36
[SID103178971]
Hepatotoxicity in CD1 mouse assessed as increased plasma GPT levels at 6 mmol/kg [AID304907, Type: Literature]
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37
[SID103178971]
Hepatotoxicity in CD1 mouse assessed as increased plasma GOT levels at 6 mmol/kg [AID304909, Type: Literature]
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38
[SID103178971]
Hepatotoxicity against HEPG2 cells at 100 uM after 6 to 8 hrs by tryptan blue exclusion test [AID304912, Type: Literature]
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39
[SID103178971]
Hepatotoxicity against HEPG2 cells at 200 uM after 6 to 8 hrs by tryptan blue exclusion test [AID304913, Type: Literature]
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40
[SID103178971]
Hepatotoxicity against human hepatocytes after 6 to 8 hrs by tryptan blue exclusion test [AID304914, Type: Literature]
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41
[SID103178971]
Induction of apoptosis in HEPG2 cells at 100 uM after 6 to 8 hrs by Hoechst staining [AID304915, Type: Literature]
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42
[SID103178971]
Induction of apoptosis in human hepatocytes after 6 to 8 hrs by Hoechst staining [AID304917, Type: Literature]
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43
[SID103178971]
Upregulation of Fas-ligand in HEPG2 cells by western blot [AID304918, Type: Literature]
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44
[SID103178971]
Upregulation of Fas-ligand in human hepatocytes by western blot [AID304919, Type: Literature]
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45
[SID103178971]
Activation of CAR in HEPG2 cells at 100 uM by western blot [AID304920, Type: Literature]
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46
[SID103178971]
Activation of CAR in human hepatocytes by western blot [AID304921, Type: Literature]
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47
[SID103178971]
Inhibition of human COX-2-mediated PGE2 production after 24 hrs [AID646028, Type: Literature]Prostaglandin G/H synthase 2 [gi:3915797]
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48
[SID103178971]
Inhibition of human CYP2C9 assessed as ratio of IC50 in absence of NADPH to IC50 for presence of NADPH using 7-methoxy-4-trifluoromethylcoumarin-3-acetic acid as substrate after 30 mins [AID678713, Type: Literature]Cytochrome P450 2C9 [gi:6686268]
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49
[SID56422763]
Luminescence-based primary cell-based high throughput screening assay to identify inhibitors of the orphan nuclear receptor subfamily 0, group B, member 1 (DAX1; NR0B1) [AID504766, Type: screening]nuclear receptor subfamily 0 group B member 1 [Homo sapiens] [gi:5016090]
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50
[SID103178971]
Cyclooxygenase inhibitor [AID742498, Type: other]Prostaglandin G/H synthase 2 [gi:3915797]
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