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stearic acid (CID 5281) - Compound BioActivity Data
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BioActivity Outcomes:
Active(18)
 
 
Inactive(555)
 
 
Inconclusive(33)
 
 
Unspecified(42)
 
 
Top Targets:
NR LBD PPAR(37)
 
 
 
 
NR LBD ER(25)
 
 
 
 
NR LBD AR(25)
 
 
 
NR LBD VDR(17)
 
 
 
NR LBD TR(17)
 
 
 
BioAssay Types:
Confirmatory(406)
 
 
 
 
Literature(143)
 
 
 
 
 
Summary(72)
 
 
 
 
Screening(2)
 
 
BioActivity Types:
Potency(419)
 
 
 
 
IC50(10)
 
 
 
 
 
Kd(9)
 
 
 
Data download

Chemical Probe    Active    Inactive    Inconclusive    Unspecified   

Total Bioassays: 349    Data Row: 648   Total Pages: 33   Display: Page     
Sort: [Click the result table header to sort]
#SubstanceActivityBioAssayTargetLinks
OutcomeTypeValue [μM]
1
[SID208012641]
Kd 0.0272Experimentally measured binding affinity data (Kd) for protein-ligand complexes derived from PDB [AID977611, Type: Literature]
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2
[SID208012641]
Kd 0.0272Experimentally measured binding affinity data (Kd) for protein-ligand complexes derived from PDB [AID977611, Type: Literature]
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3
[SID46392135]
Kd 0.28Experimentally measured binding affinity data (Kd) for protein-ligand complexes derived from PDB [AID977611, Type: Literature]Chain A, 1.4 Angstroms Structural Studies On Human Muscle Fatty Acid Binding Protein: Binding Interactions With Three Saturated And Unsaturated C18 Fatty Acids [gi:157831353]
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4
[SID46392135]
Kd 0.28Experimentally measured binding affinity data (Kd) for protein-ligand complexes derived from PDB [AID977611, Type: Literature]Chain A, 1.4 Angstroms Structural Studies On Human Muscle Fatty Acid Binding Protein: Binding Interactions With Three Saturated And Unsaturated C18 Fatty Acids [gi:157831353]
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5
[SID208013392]
Kd 0.44Experimentally measured binding affinity data (Kd) for protein-ligand complexes derived from PDB [AID977611, Type: Literature]
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6
[SID208013392]
Kd 0.44Experimentally measured binding affinity data (Kd) for protein-ligand complexes derived from PDB [AID977611, Type: Literature]
View
7
[SID144210879]
Potency-Replicate_1 0.6113qHTS assay to identify small molecule agonists of the estrogen receptor alpha (ER-alpha) signaling pathway using the BG1 cell line [AID743079, Type: confirmatory]estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627]
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8
[SID103224646]
IC50 1.1Displacement of [3H]GW2331 from Homo sapiens (human) PPARalpha receptor by scintillation proximity assay [AID1114584, Type: confirmatory]Peroxisome proliferator-activated receptor alpha [gi:3041727]
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9
[SID46392137]
Kd 1.64Experimentally measured binding affinity data (Kd) for protein-ligand complexes derived from PDB [AID977611, Type: Literature]Chain A, 1.4 Angstroms Structural Studies On Human Muscle Fatty Acid Binding Protein: Binding Interactions With Three Saturated And Unsaturated C18 Fatty Acids [gi:157831355]
View
10
[SID46392137]
Kd 1.64Experimentally measured binding affinity data (Kd) for protein-ligand complexes derived from PDB [AID977611, Type: Literature]Chain A, 1.4 Angstroms Structural Studies On Human Muscle Fatty Acid Binding Protein: Binding Interactions With Three Saturated And Unsaturated C18 Fatty Acids [gi:157831355]
View
11
[SID103224646]
IC50 6Displacement of [3H]GW2433 from Homo sapiens (human) PPARdelta receptor by scintillation proximity assay [AID1114582, Type: confirmatory]Peroxisome proliferator-activated receptor delta [gi:417522]
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12
[SID144210879]
Potency-Replicate_1 8.7076qHTS assay to identify small molecule agonists of the estrogen receptor alpha (ER-alpha) signaling pathway [AID743075, Type: confirmatory]estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627]
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13
[SID144210879]
Ratio Potency (uM) 18.058qHTS assay to identify small molecule agonists of the estrogen receptor alpha (ER-alpha) signaling pathway: Summary [AID743077, Type: summary]estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627]
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14
[SID17389656]
Potency 25.1189qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 [AID893, Type: confirmatory]Chain B, The Structure Of Wild-Type Human Hadh2 (17beta-Hydroxysteroid Dehydrogenase Type 10) Bound To Nad+ At 1.2 A [gi:122921311]
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15
[SID17389656]
Potency 25.1189qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 [AID893, Type: confirmatory]Chain A, The Structure Of Wild-Type Human Hadh2 (17beta-Hydroxysteroid Dehydrogenase Type 10) Bound To Nad+ At 1.2 A [gi:122921310]
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16
[SID103224646]
IC50 30Displacement of [3H]BRL49653 from Homo sapiens (human) PPARgamma receptor by scintillation proximity assay [AID1114583, Type: confirmatory]Peroxisome proliferator-activated receptor gamma [gi:13432234]
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17
[SID46392135]
Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature]Chain A, 1.4 Angstroms Structural Studies On Human Muscle Fatty Acid Binding Protein: Binding Interactions With Three Saturated And Unsaturated C18 Fatty Acids [gi:157831353]
View
18
[SID46392137]
Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature]Chain A, 1.4 Angstroms Structural Studies On Human Muscle Fatty Acid Binding Protein: Binding Interactions With Three Saturated And Unsaturated C18 Fatty Acids [gi:157831355]
View
19
[SID103224646]
LD50 10Cytotoxicity against mouse RAW264.7 cells [AID627981, Type: Literature]
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20
[SID103224646]
Kd 80Binding affinity against Adipocyte lipid binding protein [AID32788, Type: Literature]
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