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Oxalic Acid (CID 971) - Compound BioActivity Data
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BioActivity Outcomes:
Active(11)
 
 
Inactive(163)
 
 
Inconclusive(11)
 
 
Unspecified(3)
 
 
Top Targets:
NR LBD PPAR(16)
 
 
 
NR LBD ER(14)
 
 
 
NR LBD AR(14)
 
 
 
NR LBD Fxr(8)
 
 
NR LBD VDR(8)
 
 
 
BioAssay Types:
Confirmatory(124)
 
 
 
Summary(48)
 
 
 
Literature(14)
 
 
 
BioActivity Types:
Potency(160)
 
 
 
Ki(6)
 
 
IC50(3)
 
 
 
Data download

Chemical Probe    Active    Inactive    Inconclusive    Unspecified   

Total Bioassays: 94    Data Row: 188   Total Pages: 10   Display: Page     
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#SubstanceActivityBioAssayTargetLinks
OutcomeTypeValue [μM]
1
[SID46394048]
Ki 17Experimentally measured binding affinity data (Ki) for protein-ligand complexes derived from PDB [AID977610, Type: Literature]Chain A, Crystal Structure Of Phosphonopyruvate Hydrolase Complex With Oxalate And Mg++ [gi:116667098]
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2
[SID46394048]
Ki 17Experimentally measured binding affinity data (Ki) for protein-ligand complexes derived from PDB [AID977610, Type: Literature]Chain A, Crystal Structure Of Phosphonopyruvate Hydrolase Complex With Oxalate And Mg++ [gi:116667098]
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3
[SID46393204]
Ki 24Experimentally measured binding affinity data (Ki) for protein-ligand complexes derived from PDB [AID977610, Type: Literature]Chain A, Human Pyruvate Kinase M2 [gi:73535278]
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4
[SID46393204]
Ki 24Experimentally measured binding affinity data (Ki) for protein-ligand complexes derived from PDB [AID977610, Type: Literature]Chain A, Human Pyruvate Kinase M2 [gi:73535278]
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5
[SID46394255]
Ki 280Experimentally measured binding affinity data (Ki) for protein-ligand complexes derived from PDB [AID977610, Type: Literature]Chain A, Structure Of Phosphorylated Enzyme I Of The Phosphoenolpyruvate:sugar Phosphotransferase System [gi:119389970]
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6
[SID46394255]
Ki 280Experimentally measured binding affinity data (Ki) for protein-ligand complexes derived from PDB [AID977610, Type: Literature]Chain A, Structure Of Phosphorylated Enzyme I Of The Phosphoenolpyruvate:sugar Phosphotransferase System [gi:119389970]
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7
[SID46392737]
IC50 40000Experimentally measured binding affinity data (IC50) for protein-ligand complexes derived from PDB [AID977608, Type: Literature]Chain A, Crystal Structure Of Sh2 In Complex With Oxalic Acid. [gi:46015003]
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8
[SID46392737]
IC50 40000Experimentally measured binding affinity data (IC50) for protein-ligand complexes derived from PDB [AID977608, Type: Literature]Chain A, Crystal Structure Of Sh2 In Complex With Oxalic Acid. [gi:46015003]
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9
[SID46394048]
Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature]Chain A, Crystal Structure Of Phosphonopyruvate Hydrolase Complex With Oxalate And Mg++ [gi:116667098]
View
10
[SID46394255]
Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature]Chain A, Structure Of Phosphorylated Enzyme I Of The Phosphoenolpyruvate:sugar Phosphotransferase System [gi:119389970]
View
11
[SID46392737]
Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature]Chain A, Crystal Structure Of Sh2 In Complex With Oxalic Acid. [gi:46015003]
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12
[SID103393333]
IC50 40000Inhibitory activity against SH2 domain of human p60 c-Src tyrosine kinase using surface plasmon resonance (SPR) assay. [AID224309, Type: Literature]
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13
[SID103393333]
Binding energy by using the equation deltaG obsd = -RT ln KD [AID227718, Type: Literature]
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14
[SID103393333]
TP_TRANSPORTER: inhibition of E1S uptake (E1S: 0.00476 uM, oxalic acid: 10000 uM) in OATP-B-expressing HEK293 cells [AID679442, Type: Literature]Solute carrier organic anion transporter family member 2B1 [gi:313104012]
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15
[SID144209320]
Potency-Replicate_1 qHTS assay to identify small molecule agonists of the farnesoid-X-receptor (FXR) signaling pathway [AID743220, Type: confirmatory]farnesoid X nuclear receptor [Homo sapiens] [gi:325495553]
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16
[SID144209320]
Potency-Replicate_1 qHTS assay to identify small molecule antagonists of the farnesoid-X-receptor (FXR) signaling pathway [AID743217, Type: confirmatory]farnesoid X nuclear receptor [Homo sapiens] [gi:325495553]
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17
[SID144209320]
Ratio Potency (uM) qHTS assay to identify small molecule agonists of the farnesoid-X-receptor (FXR) signaling pathway: Summary [AID743239, Type: summary]farnesoid X nuclear receptor [Homo sapiens] [gi:325495553]
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18
[SID144209320]
qHTS assay to identify small molecule antagonists of the farnesoid-X-receptor (FXR) signaling pathway: Summary [AID743240, Type: summary]farnesoid X nuclear receptor [Homo sapiens] [gi:325495553]
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19
[SID144213663]
Ratio Potency (uM) qHTS assay to identify small molecule agonists of the farnesoid-X-receptor (FXR) signaling pathway: Summary [AID743239, Type: summary]farnesoid X nuclear receptor [Homo sapiens] [gi:325495553]
View
20
[SID144213663]
qHTS assay to identify small molecule antagonists of the farnesoid-X-receptor (FXR) signaling pathway: Summary [AID743240, Type: summary]farnesoid X nuclear receptor [Homo sapiens] [gi:325495553]
View