| 1 | [SID103201463] | Active | Ki | 0.00023 | Inhibition constant against HIV-1 Protease [AID160455, Type: Literature] | Pol polyprotein [gi:75593047] |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | Ki | 0.00023 [uM] | | BioAssay | Inhibition constant against HIV-1 Protease | | AID | 160455 | | BioAssay type | Literature | | Target | Pol polyprotein [gi:75593047] | | PubMed | 12459011 | | Data Table |  |
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| 2 | [SID103201463] | Active | Kd | 0.00113 | Equilibrium constant for the interaction between inhibitor and HIV-1 Protease [AID162706, Type: Literature] | Pol polyprotein [gi:75593047] |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | Kd | 0.00113 [uM] | | BioAssay | Equilibrium constant for the interaction between inhibitor and HIV-1 Protease | | AID | 162706 | | BioAssay type | Literature | | Target | Pol polyprotein [gi:75593047] | | PubMed | 12459011 | | Data Table |  |
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| 3 | [SID103201463] | Active | IC50 | 0.1 | Inhibition of p60c-src expressed in chick embryo fibroblast [AID358183, Type: other] | |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | IC50 | 0.1 [uM] | | BioAssay | Inhibition of p60c-src expressed in chick embryo fibroblast | | AID | 358183 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 4 | [SID103201463] | Active | IC50 | 0.14 | Inhibition of FBPase in human liver using fructose-2,6phosphate as a substrate [AID453457, Type: Literature] | Fructose-1,6-bisphosphatase 1 [gi:311033495] |   View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | IC50 | 0.14 [uM] | | BioAssay | Inhibition of FBPase in human liver using fructose-2,6phosphate as a substrate | | AID | 453457 | | BioAssay type | Literature | | Target | Fructose-1,6-bisphosphatase 1 [gi:311033495] | | PubMed | 19969452 | | Data Table |  |
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| 5 | [SID103201463] | Active | IC50 | 0.3 | Inhibition of Rous sarcoma virus p60 v-src-induced IgG phosphorylation in tumor bearing rabbits by SDS PAGE [AID358182, Type: other] | |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | IC50 | 0.3 [uM] | | BioAssay | Inhibition of Rous sarcoma virus p60 v-src-induced IgG phosphorylation in tumor bearing rabbits by SDS PAGE | | AID | 358182 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 6 | [SID103201463] | Active | IC50 | 0.44 | Inhibition of FBPase in human liver [AID453456, Type: Literature] | Fructose-1,6-bisphosphatase 1 [gi:311033495] |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | IC50 | 0.44 [uM] | | BioAssay | Inhibition of FBPase in human liver | | AID | 453456 | | BioAssay type | Literature | | Target | Fructose-1,6-bisphosphatase 1 [gi:311033495] | | PubMed | 19969452 | | Data Table |  |
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| 7 | [SID103201463] | Active | IC50 | 0.8 | Concentration required to inhibit the human liver recombinant fructose-1,6-bisphosphatase. [AID89523, Type: Literature] | |   View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | IC50 | 0.8 [uM] | | BioAssay | Concentration required to inhibit the human liver recombinant fructose-1,6-bisphosphatase. | | AID | 89523 | | BioAssay type | Literature | | Target | | | PubMed | 11140724 | | Data Table |  |
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| 8 | [SID103201463] | Active | IC50 | 1 | Inhibition of human liver FBPase expressed in Escherichia coli by spectrophotometry [AID354019, Type: Literature] | Fructose-1,6-bisphosphatase 1 [gi:311033495] |   View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | IC50 | 1 [uM] | | BioAssay | Inhibition of human liver FBPase expressed in Escherichia coli by spectrophotometry | | AID | 354019 | | BioAssay type | Literature | | Target | Fructose-1,6-bisphosphatase 1 [gi:311033495] | | PubMed | 19348494 | | Data Table |  |
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| 9 | [SID103201463] | Active | IC50 | 1 | Inhibition of rat FBPase [AID580981, Type: other] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | IC50 | 1 [uM] | | BioAssay | Inhibition of rat FBPase | | AID | 580981 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 10 | [SID103201463] | Active | IC50 | 1.3 | Inhibition of pig FBPase expressed in Escherichia coli EK1601 by spectrophotometry [AID419859, Type: Literature] | Fructose-1,6-bisphosphatase 1 [gi:1706735] |   View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | IC50 | 1.3 [uM] | | BioAssay | Inhibition of pig FBPase expressed in Escherichia coli EK1601 by spectrophotometry | | AID | 419859 | | BioAssay type | Literature | | Target | Fructose-1,6-bisphosphatase 1 [gi:1706735] | | PubMed | 19419876 | | Data Table |  |
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| 11 | [SID103201463] | Active | IC50 | 1.3 | Inhibition of pig kidney fructose-1,6-bisphosphatase expressed in Escherichia coli BL21 (DE3) assessed as reduction of NADP+ to NADPH by phosphoglucose isomerase/glucose-6-phosphate dehydrogenase coupled assay [AID477766, Type: Literature] | Fructose-1,6-bisphosphatase 1 [gi:1706735] |   View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | IC50 | 1.3 [uM] | | BioAssay | Inhibition of pig kidney fructose-1,6-bisphosphatase expressed in Escherichia coli BL21 (DE3) assessed as reduction of NADP+ to NADPH by phosphoglucose isomerase/glucose-6-phosphate dehydrogenase coupled assay | | AID | 477766 | | BioAssay type | Literature | | Target | Fructose-1,6-bisphosphatase 1 [gi:1706735] | | PubMed | 20116906 | | Data Table |  |
|
| 12 | [SID103201463] | Active | EC50 | 1.4 | Activation of rat GPPase [AID580980, Type: other] | |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | EC50 | 1.4 [uM] | | BioAssay | Activation of rat GPPase | | AID | 580980 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 13 | [SID103201463] | Active | Kd | 2.7 | Dissociation constant of the compound [AID238114, Type: Literature] | |   View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | Kd | 2.7 [uM] | | BioAssay | Dissociation constant of the compound | | AID | 238114 | | BioAssay type | Literature | | Target | | | PubMed | 15293991 | | Data Table |  |
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| 14 | [SID103201463] | Active | EC50 | 3.5 | Measure of Agonist Potency at turkey Purinoceptor P2Y1 stably expressed in 131N1 astrocytoma cell [AID165253, Type: Literature] | |   View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | EC50 | 3.5 [uM] | | BioAssay | Measure of Agonist Potency at turkey Purinoceptor P2Y1 stably expressed in 131N1 astrocytoma cell | | AID | 165253 | | BioAssay type | Literature | | Target | | | PubMed | 11754592 | | Data Table |  |
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| 15 | [SID103201463] | Active | EC50 | 3.7 | Measure of Agonist Potency at human P2Y purinoceptor 2 (hP2Y2) stably expressed in 131N1 astrocytoma cell [AID150498, Type: Literature] | |   View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | EC50 | 3.7 [uM] | | BioAssay | Measure of Agonist Potency at human P2Y purinoceptor 2 (hP2Y2) stably expressed in 131N1 astrocytoma cell | | AID | 150498 | | BioAssay type | Literature | | Target | | | PubMed | 11754592 | | Data Table |  |
|
| 16 | [SID103201463] | Active | Kd | 5.4 | Displacement of [35S]APS from Mycobacterium tuberculosis adenosine-5'-phosphosulfate reductase by liquid scintillation counting [AID440580, Type: Literature] | |   View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | Kd | 5.4 [uM] | | BioAssay | Displacement of [35S]APS from Mycobacterium tuberculosis adenosine-5'-phosphosulfate reductase by liquid scintillation counting | | AID | 440580 | | BioAssay type | Literature | | Target | | | PubMed | 19678707 | | Data Table |  |
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| 17 | [SID103201463] | Active | Kd | 5.4 | Binding affinity to Mycobacterium tuberculosis adenosine-5'-phosphosulfate reductase assessed as S-sulfocysteine formation at pH 7.5 by single turnover method in absence of MgCl2 [AID440581, Type: Literature] | |   View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | Kd | 5.4 [uM] | | BioAssay | Binding affinity to Mycobacterium tuberculosis adenosine-5'-phosphosulfate reductase assessed as S-sulfocysteine formation at pH 7.5 by single turnover method in absence of MgCl2 | | AID | 440581 | | BioAssay type | Literature | | Target | | | PubMed | 19678707 | | Data Table |  |
|
| 18 | [SID103201463] | Active | EC50 | 5.9 | Activation of human AMPK after 15 mins [AID580978, Type: other] | |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | EC50 | 5.9 [uM] | | BioAssay | Activation of human AMPK after 15 mins | | AID | 580978 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 19 | [SID103201463] | Active | EC50 | 7.2 | Measure of Agonist Potency at human P2Y purinoceptor 1 (hP2Y1) stably expressed in 131N1 astrocytoma cell [AID150332, Type: Literature] | |   View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | EC50 | 7.2 [uM] | | BioAssay | Measure of Agonist Potency at human P2Y purinoceptor 1 (hP2Y1) stably expressed in 131N1 astrocytoma cell | | AID | 150332 | | BioAssay type | Literature | | Target | | | PubMed | 11754592 | | Data Table |  |
|
| 20 | [SID103201463] | Active | IC50 | 9.8 | Inhibition of human liver fructose-1,6-bisphosphatase expressed in Escherichia coli BL21 (DE3) assessed as reduction of NADP+ to NADPH by phosphoglucose isomerase/glucose-6-phosphate dehydrogenase coupled assay [AID477767, Type: Literature] | Fructose-1,6-bisphosphatase 1 [gi:311033495] |   View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | IC50 | 9.8 [uM] | | BioAssay | Inhibition of human liver fructose-1,6-bisphosphatase expressed in Escherichia coli BL21 (DE3) assessed as reduction of NADP+ to NADPH by phosphoglucose isomerase/glucose-6-phosphate dehydrogenase coupled assay | | AID | 477767 | | BioAssay type | Literature | | Target | Fructose-1,6-bisphosphatase 1 [gi:311033495] | | PubMed | 20116906 | | Data Table |  |
|
| 21 | [SID103201463] | Active | IC50 | 12.3 | Inhibition of human recombinant FBPase using fructose-1,6-biphosphate as substrate incubated for 3 mins prior to substrate addition by spectrophotometric analysis [AID684832, Type: other] | |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | IC50 | 12.3 [uM] | | BioAssay | Inhibition of human recombinant FBPase using fructose-1,6-biphosphate as substrate incubated for 3 mins prior to substrate addition by spectrophotometric analysis | | AID | 684832 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 22 | [SID103201463] | Active | Km | 14 | Activity at ecto-5'-nucleotidase [AID448478, Type: Literature] | |   View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | Km | 14 [uM] | | BioAssay | Activity at ecto-5'-nucleotidase | | AID | 448478 | | BioAssay type | Literature | | Target | | | PubMed | 19580286 | | Data Table |  |
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| 23 | [SID103201463] | Active | EC50 | 17.25 | Measure of Agonist Potency at human P2Y purinoceptor 11 (hP2Y11) stably expressed in 131N1 astrocytoma cell at 10 uM [AID150488, Type: Literature] | |   View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | EC50 | 17.25 [uM] | | BioAssay | Measure of Agonist Potency at human P2Y purinoceptor 11 (hP2Y11) stably expressed in 131N1 astrocytoma cell at 10 uM | | AID | 150488 | | BioAssay type | Literature | | Target | | | PubMed | 11754592 | | Data Table |  |
|
| 24 | [SID103201463] | Active | Kd | 21 | Binding affinity to Mycobacterium tuberculosis adenosine-5'-phosphosulfate reductase assessed as S-sulfocysteine formation at pH 7.5 by single turnover method in presence of 0.5 mM MgCl2 [AID440582, Type: Literature] | |   View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | Kd | 21 [uM] | | BioAssay | Binding affinity to Mycobacterium tuberculosis adenosine-5'-phosphosulfate reductase assessed as S-sulfocysteine formation at pH 7.5 by single turnover method in presence of 0.5 mM MgCl2 | | AID | 440582 | | BioAssay type | Literature | | Target | | | PubMed | 19678707 | | Data Table |  |
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| 25 | [SID103201463] | Active | Kd | 31 | Binding affinity to Mycobacterium tuberculosis adenosine-5'-phosphosulfate reductase assessed as S-sulfocysteine formation at pH 7.5 by single turnover method in presence of 2 mM MgCl2 [AID440583, Type: Literature] | |   View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | Kd | 31 [uM] | | BioAssay | Binding affinity to Mycobacterium tuberculosis adenosine-5'-phosphosulfate reductase assessed as S-sulfocysteine formation at pH 7.5 by single turnover method in presence of 2 mM MgCl2 | | AID | 440583 | | BioAssay type | Literature | | Target | | | PubMed | 19678707 | | Data Table |  |
|
| 26 | [SID103201463] | Active | Km | 32.8 | Activity of recombinant human ADAL1 expressed in Escherichia coli by UV-spectrophotometry [AID612651, Type: Literature] | Adenosine deaminase-like protei [gi:146286026] |   View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | Km | 32.8 [uM] | | BioAssay | Activity of recombinant human ADAL1 expressed in Escherichia coli by UV-spectrophotometry | | AID | 612651 | | BioAssay type | Literature | | Target | Adenosine deaminase-like protei [gi:146286026] | | PubMed | 21755941 | | Data Table |  |
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| 27 | [SID103201463] | Active | Ki | 38 | Inhibition constant was evaluated against horse liver alcohol dehydrogenase [AID33710, Type: Literature] | |   View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | Ki | 38 [uM] | | BioAssay | Inhibition constant was evaluated against horse liver alcohol dehydrogenase | | AID | 33710 | | BioAssay type | Literature | | Target | | | PubMed | 7021832 | | Data Table |  |
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| 28 | [SID103201463] | Active | | | Tested for relaxation of carbachol-contracted guinea pig taenia coli at 37 degree C; Significantly less potent than ATP [AID77361, Type: Literature] | |   View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | BioAssay | Tested for relaxation of carbachol-contracted guinea pig taenia coli at 37 degree C; Significantly less potent than ATP | | AID | 77361 | | BioAssay type | Literature | | Target | | | PubMed | 8254622 | | Data Table |  |
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| 29 | [SID48415520] | Active | | | DSSTox (FDAMDD) FDA Maximum (Recommended) Daily Dose Database [AID1195, Type: other] | |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 48415520 | | CID | 6083 | | Outcome | Active | | BioAssay | DSSTox (FDAMDD) FDA Maximum (Recommended) Daily Dose Database | | AID | 1195 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 30 | [SID103201463] | Active | | | Measure of Agonist Potency at human P2Y purinoceptor 4 (hP2Y4) stably expressed in 131N1 astrocytoma cell; Antagonist effect [AID150626, Type: Literature] | |   View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | BioAssay | Measure of Agonist Potency at human P2Y purinoceptor 4 (hP2Y4) stably expressed in 131N1 astrocytoma cell; Antagonist effect | | AID | 150626 | | BioAssay type | Literature | | Target | | | PubMed | 11754592 | | Data Table |  |
|
| 31 | [SID103201463] | Active | Ki | | Binding affinity to Mycobacterium tuberculosis adenosine-5'-phosphosulfate reductase assessed as S-sulfocysteine formation at pH 5.5 by single turnover method in absence of thioredoxin [AID440574, Type: Literature] | |   View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | Ki | [uM] | | BioAssay | Binding affinity to Mycobacterium tuberculosis adenosine-5'-phosphosulfate reductase assessed as S-sulfocysteine formation at pH 5.5 by single turnover method in absence of thioredoxin | | AID | 440574 | | BioAssay type | Literature | | Target | | | PubMed | 19678707 | | Data Table |  |
|
| 32 | [SID103201463] | Active | | | Inhibition of Escherichia coli KPR at 1 mM [AID269131, Type: Literature] | |   View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 103201463 | | CID | 6083 | | Outcome | Active | | BioAssay | Inhibition of Escherichia coli KPR at 1 mM | | AID | 269131 | | BioAssay type | Literature | | Target | | | PubMed | 16884311 | | Data Table |  |
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| 33 | [SID46392931] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Structural Basis For The Activation Of Glycogen Phosphorylase B By Adenosine Monophosphate [gi:494494] |   View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 46392931 | | CID | 6083 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Structural Basis For The Activation Of Glycogen Phosphorylase B By Adenosine Monophosphate [gi:494494] | | PubMed | 1962195 | | Data Table |  |
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| 34 | [SID46393301] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Crystal Structure Of An Adp-Dependent Glucokinase From Pyrococcus Furiosus [gi:46015797] |   View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 46393301 | | CID | 6083 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Crystal Structure Of An Adp-Dependent Glucokinase From Pyrococcus Furiosus [gi:46015797] | | PubMed | 12909015 | | Data Table |  |
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| 35 | [SID46393711] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Ribonuclease A- Amp Complex [gi:75765679] |   View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 46393711 | | CID | 6083 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Ribonuclease A- Amp Complex [gi:75765679] | | PubMed | 16045769 | | Data Table |  |
|
| 36 | [SID46394204] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Structure Of Xac Nucleotide Pyrophosphatase/phosphodiesterase In Complex With Amp [gi:112490889] |   View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 46394204 | | CID | 6083 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Structure Of Xac Nucleotide Pyrophosphatase/phosphodiesterase In Complex With Amp [gi:112490889] | | PubMed | 16893180 | | Data Table |  |
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| 37 | [SID46394436] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Structural Mechanism For Glycogen Phosphorylase Control By Phosphorylation And Amp [gi:231257] |   View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 46394436 | | CID | 6083 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Structural Mechanism For Glycogen Phosphorylase Control By Phosphorylation And Amp [gi:231257] | | PubMed | 1900534 | | Data Table |  |
|
| 38 | [SID46394446] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Structural Mechanism For Glycogen Phosphorylase Control By Phosphorylation And Amp [gi:157837173] |   View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 46394446 | | CID | 6083 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Structural Mechanism For Glycogen Phosphorylase Control By Phosphorylation And Amp [gi:157837173] | | PubMed | 1900534 | | Data Table |  |
|