| 1 | [SID103284478] | Active | IC50 | 0.15 | Inhibition of human recombinant aldose reductase [AID322413, Type: Literature] | Aldose reductase [gi:113596] |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | IC50 | 0.15 [uM] | | BioAssay | Inhibition of human recombinant aldose reductase | | AID | 322413 | | BioAssay type | Literature | | Target | Aldose reductase [gi:113596] | | PubMed | 18165015 | | Data Table |  |
|
| 2 | [SID103284478] | Active | IC50 | 0.16 | Inhibition of rat lens aldose reductase [AID385353, Type: Literature] | Aldose reductase [gi:1168407] |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | IC50 | 0.16 [uM] | | BioAssay | Inhibition of rat lens aldose reductase | | AID | 385353 | | BioAssay type | Literature | | Target | Aldose reductase [gi:1168407] | | PubMed | 18298080 | | Data Table |  |
|
| 3 | [SID103284478] | Active | IC50 | 2 | Inhibition of human recombinant aldose reductase using D-glyceraldehyde as substrate preincubated for 10 mins before substrate addition measured for every 10 secs for 50 mins by spectrophotometry [AID639825, Type: Literature] | Aldose reductase [gi:113596] |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | IC50 | 2 [uM] | | BioAssay | Inhibition of human recombinant aldose reductase using D-glyceraldehyde as substrate preincubated for 10 mins before substrate addition measured for every 10 secs for 50 mins by spectrophotometry | | AID | 639825 | | BioAssay type | Literature | | Target | Aldose reductase [gi:113596] | | PubMed | 22261024 | | Data Table |  |
|
| 4 | [SID85149171] | Active | AC50 | 2.48 | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity [AID602350, Type: confirmatory] | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | AC50 | 2.48 [uM] | | BioAssay | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity | | AID | 602350 | | BioAssay type | confirmatory | | Target | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] | | PubMed | | | Data Table |  |
|
| 5 | [SID85149171] | Active | AC50 | 2.48 | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity [AID602350, Type: confirmatory] | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | AC50 | 2.48 [uM] | | BioAssay | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity | | AID | 602350 | | BioAssay type | confirmatory | | Target | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] | | PubMed | | | Data Table |  |
|
| 6 | [SID85149171] | Active | AC50 | 2.48 | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity_Set2 [AID624274, Type: confirmatory] | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | AC50 | 2.48 [uM] | | BioAssay | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity_Set2 | | AID | 624274 | | BioAssay type | confirmatory | | Target | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] | | PubMed | | | Data Table |  |
|
| 7 | [SID85149171] | Active | AC50 | 2.48 | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity_Set2 [AID624274, Type: confirmatory] | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | AC50 | 2.48 [uM] | | BioAssay | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity_Set2 | | AID | 624274 | | BioAssay type | confirmatory | | Target | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] | | PubMed | | | Data Table |  |
|
| 8 | [SID103284478] | Active | IC50 | 8.1 | Antioxidant activity assessed as superoxide-scavenging activity by nitrite method [AID399341, Type: Literature] | |   View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | IC50 | 8.1 [uM] | | BioAssay | Antioxidant activity assessed as superoxide-scavenging activity by nitrite method | | AID | 399341 | | BioAssay type | Literature | | Target | | | PubMed | 9461655 | | Data Table |  |
|
| 9 | [SID103284478] | Active | IC50 | 9 | Antialgal activity against Microcystis aeruginosa NIES 44 after 24 hrs by fluorophotometric method [AID337227, Type: other] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | IC50 | 9 [uM] | | BioAssay | Antialgal activity against Microcystis aeruginosa NIES 44 after 24 hrs by fluorophotometric method | | AID | 337227 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 10 | [SID103284478] | Active | IC50 | 10 | In vitro inhibition of partially purified calf lens aldose reductase; value ranges from 10E-5 to 10E-6 [AID34503, Type: Literature] | |   View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | IC50 | 10 [uM] | | BioAssay | In vitro inhibition of partially purified calf lens aldose reductase; value ranges from 10E-5 to 10E-6 | | AID | 34503 | | BioAssay type | Literature | | Target | | | PubMed | 3121857 | | Data Table |  |
|
| 11 | [SID103284478] | Active | IC50 | 12.46 | Inhibition of human RNase H by FRET assay [AID362726, Type: Literature] | |   View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | IC50 | 12.46 [uM] | | BioAssay | Inhibition of human RNase H by FRET assay | | AID | 362726 | | BioAssay type | Literature | | Target | | | PubMed | 18763827 | | Data Table |  |
|
| 12 | [SID103284478] | Active | IC50 | 14.74 | Inhibition of xanthine oxidase-mediated formation of uric acid by spectrophotometry [AID336485, Type: Literature] | |   View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | IC50 | 14.74 [uM] | | BioAssay | Inhibition of xanthine oxidase-mediated formation of uric acid by spectrophotometry | | AID | 336485 | | BioAssay type | Literature | | Target | | | PubMed | 12444671 | | Data Table |  |
|
| 13 | [SID103284478] | Active | IC50 | 21.27 | Inhibition of HIV2 RNase H by FRET assay [AID362724, Type: Literature] | |   View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | IC50 | 21.27 [uM] | | BioAssay | Inhibition of HIV2 RNase H by FRET assay | | AID | 362724 | | BioAssay type | Literature | | Target | | | PubMed | 18763827 | | Data Table |  |
|
| 14 | [SID103284478] | Active | IC50 | 25 | Inhibition of Pim2 kinase [AID327000, Type: Literature] | |   View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | IC50 | 25 [uM] | | BioAssay | Inhibition of Pim2 kinase | | AID | 327000 | | BioAssay type | Literature | | Target | | | PubMed | 18163587 | | Data Table |  |
|
| 15 | [SID85149171] | Active | AC50 | 29.77 | Luminescence Cell-Free Homogeneous Dose Retest to Confirm Inhibitors of GSK-3 alpha [AID463203, Type: confirmatory] | GSK3A gene product [Homo sapiens] [gi:49574532] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | AC50 | 29.77 [uM] | | BioAssay | Luminescence Cell-Free Homogeneous Dose Retest to Confirm Inhibitors of GSK-3 alpha | | AID | 463203 | | BioAssay type | confirmatory | | Target | GSK3A gene product [Homo sapiens] [gi:49574532] | | PubMed | | | Data Table |  |
|
| 16 | [SID85149171] | Active | AC50 | 29.77 | Luminescence Cell-Free Homogeneous Dose Retest to Confirm Inhibitors of GSK-3 alpha [AID463203, Type: confirmatory] | GSK3A gene product [Homo sapiens] [gi:49574532] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | AC50 | 29.77 [uM] | | BioAssay | Luminescence Cell-Free Homogeneous Dose Retest to Confirm Inhibitors of GSK-3 alpha | | AID | 463203 | | BioAssay type | confirmatory | | Target | GSK3A gene product [Homo sapiens] [gi:49574532] | | PubMed | | | Data Table |  |
|
| 17 | [SID103284478] | Active | IC50 | 33.3 | Inhibition of mouse recombinant AKR1C21 [AID322409, Type: Literature] | Aldo-keto reductase family 1 member C21 [gi:172045824] |   View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | IC50 | 33.3 [uM] | | BioAssay | Inhibition of mouse recombinant AKR1C21 | | AID | 322409 | | BioAssay type | Literature | | Target | Aldo-keto reductase family 1 member C21 [gi:172045824] | | PubMed | 18165015 | | Data Table |  |
|
| 18 | [SID85149171] | Active | Potency | 35.4813 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | Potency | 35.4813 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Iota | | AID | 588590 | | BioAssay type | confirmatory | | Target | DNA polymerase iota [Homo sapiens] [gi:154350220] | | PubMed | | | Data Table |  |
|
| 19 | [SID85149171] | Active | Potency | 35.4813 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | Potency | 35.4813 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Iota | | AID | 588590 | | BioAssay type | confirmatory | | Target | DNA polymerase iota [Homo sapiens] [gi:154350220] | | PubMed | | | Data Table |  |
|
| 20 | [SID85149171] | Active | Potency | 44.6684 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | Potency | 44.6684 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 21 | [SID85149171] | Active | Potency | 44.6684 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | Potency | 44.6684 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 22 | [SID103284478] | Active | IC50 | 45 | Antialgal activity against Anabaena flos-aquae NIES 73 after 48 hrs by fluorophotometric method [AID337228, Type: other] | |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | IC50 | 45 [uM] | | BioAssay | Antialgal activity against Anabaena flos-aquae NIES 73 after 48 hrs by fluorophotometric method | | AID | 337228 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 23 | [SID103284478] | Active | | | Growth inhibition of BALB/c mouse cloned 3T3/A31 cells at 100 ug/mL after 72 hrs by nigrosin assay [AID379093, Type: Literature] | |   View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | BioAssay | Growth inhibition of BALB/c mouse cloned 3T3/A31 cells at 100 ug/mL after 72 hrs by nigrosin assay | | AID | 379093 | | BioAssay type | Literature | | Target | | | PubMed | 10096863 | | Data Table |  |
|
| 24 | [SID103284478] | Active | | | Cytotoxicity against african green monkey Vero cells after 3 days by MTT assay [AID469284, Type: Literature] | |   View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | BioAssay | Cytotoxicity against african green monkey Vero cells after 3 days by MTT assay | | AID | 469284 | | BioAssay type | Literature | | Target | | | PubMed | 19778089 | | Data Table |  |
|
| 25 | [SID103284478] | Active | | | Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS/IFN-gamma-induced NO production at 25 to 100 uM after 20 hrs by Griess method [AID646459, Type: Literature] | |   View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Active | | BioAssay | Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS/IFN-gamma-induced NO production at 25 to 100 uM after 20 hrs by Griess method | | AID | 646459 | | BioAssay type | Literature | | Target | | | PubMed | 22281186 | | Data Table |  |
|
| 26 | [SID85149171] | Active | | | uHTS Luminescent assay for identification of inhibitors of human intestinal alkaline phosphatase [AID2544, Type: screening] | Alkaline phosphatase, intestinal [Homo sapiens] [gi:124376142] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | BioAssay | uHTS Luminescent assay for identification of inhibitors of human intestinal alkaline phosphatase | | AID | 2544 | | BioAssay type | screening | | Target | Alkaline phosphatase, intestinal [Homo sapiens] [gi:124376142] | | PubMed | | | Data Table |  |
|
| 27 | [SID85149171] | Active | | | uHTS Luminescent assay for identification of inhibitors of human intestinal alkaline phosphatase [AID2544, Type: screening] | Alkaline phosphatase, intestinal [Homo sapiens] [gi:124376142] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | BioAssay | uHTS Luminescent assay for identification of inhibitors of human intestinal alkaline phosphatase | | AID | 2544 | | BioAssay type | screening | | Target | Alkaline phosphatase, intestinal [Homo sapiens] [gi:124376142] | | PubMed | | | Data Table |  |
|
| 28 | [SID85149171] | Active | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of human platelet-activating factor acetylhydrolase 1B, catalytic subunit 3 (PAFAH1B3) [AID492972, Type: screening] | platelet-activating factor acetylhydrolase IB subunit gamma [Homo sapiens] [gi:225543099] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of human platelet-activating factor acetylhydrolase 1B, catalytic subunit 3 (PAFAH1B3) | | AID | 492972 | | BioAssay type | screening | | Target | platelet-activating factor acetylhydrolase IB subunit gamma [Homo sapiens] [gi:225543099] | | PubMed | | | Data Table |  |
|
| 29 | [SID85149171] | Active | | | HTS-Luminescent assay for inhibitors of ALR by detection of hydrogen peroxide production Measured in Biochemical System Using Plate Reader - 2036-02_Inhibitor_SinglePoint_HTS [AID485317, Type: screening] | FAD-linked sulfhydryl oxidase ALR [Homo sapiens] [gi:54112432] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | BioAssay | HTS-Luminescent assay for inhibitors of ALR by detection of hydrogen peroxide production Measured in Biochemical System Using Plate Reader - 2036-02_Inhibitor_SinglePoint_HTS | | AID | 485317 | | BioAssay type | screening | | Target | FAD-linked sulfhydryl oxidase ALR [Homo sapiens] [gi:54112432] | | PubMed | | | Data Table |  |
|
| 30 | [SID85149171] | Active | | | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_SinglePoint_HTS_Activity [AID588391, Type: screening] | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | BioAssay | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 588391 | | BioAssay type | screening | | Target | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] | | PubMed | | | Data Table |  |
|
| 31 | [SID85149171] | Active | | | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_SinglePoint_HTS_Activity [AID588391, Type: screening] | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | BioAssay | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 588391 | | BioAssay type | screening | | Target | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] | | PubMed | | | Data Table |  |
|
| 32 | [SID85149171] | Active | | | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) [AID588664, Type: screening] | ABL1 gene product [Homo sapiens] [gi:62362414] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | BioAssay | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) | | AID | 588664 | | BioAssay type | screening | | Target | ABL1 gene product [Homo sapiens] [gi:62362414] | | PubMed | | | Data Table |  |
|
| 33 | [SID85149171] | Active | | | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) [AID588664, Type: screening] | ABL1 gene product [Homo sapiens] [gi:62362414] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | BioAssay | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) | | AID | 588664 | | BioAssay type | screening | | Target | ABL1 gene product [Homo sapiens] [gi:62362414] | | PubMed | | | Data Table |  |
|
| 34 | [SID85149171] | Active | | | TRFRET-based biochemical high throughput confirmation assay for inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) [AID602124, Type: screening] | ABL1 gene product [Homo sapiens] [gi:62362414] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | BioAssay | TRFRET-based biochemical high throughput confirmation assay for inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) | | AID | 602124 | | BioAssay type | screening | | Target | ABL1 gene product [Homo sapiens] [gi:62362414] | | PubMed | | | Data Table |  |
|
| 35 | [SID85149171] | Active | | | TRFRET-based biochemical high throughput confirmation assay for inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) [AID602124, Type: screening] | ABL1 gene product [Homo sapiens] [gi:62362414] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Active | | BioAssay | TRFRET-based biochemical high throughput confirmation assay for inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) | | AID | 602124 | | BioAssay type | screening | | Target | ABL1 gene product [Homo sapiens] [gi:62362414] | | PubMed | | | Data Table |  |
|
| 36 | [SID103284478] | Unspecified | IC50 | 0.1 | In vitro inhibitory activity towards partially purified rat lens aldose reductase [AID34809, Type: Literature] | |   View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Unspecified | | IC50 | 0.1 [uM] | | BioAssay | In vitro inhibitory activity towards partially purified rat lens aldose reductase | | AID | 34809 | | BioAssay type | Literature | | Target | | | PubMed | 3121857 | | Data Table |  |
|
| 37 | [SID103284478] | Unspecified | IC50 | 22.3 | Inhibition of HIV1 RNase H by FRET assay [AID362723, Type: Literature] | |   View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Unspecified | | IC50 | 22.3 [uM] | | BioAssay | Inhibition of HIV1 RNase H by FRET assay | | AID | 362723 | | BioAssay type | Literature | | Target | | | PubMed | 18763827 | | Data Table |  |
|
| 38 | [SID103284478] | Unspecified | IC50 | 100 | Inhibition of xanthine oxidase assessed as decrease in uric acid production by spectrophotometry [AID399340, Type: Literature] | |   View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Unspecified | | IC50 | 100 [uM] | | BioAssay | Inhibition of xanthine oxidase assessed as decrease in uric acid production by spectrophotometry | | AID | 399340 | | BioAssay type | Literature | | Target | | | PubMed | 9461655 | | Data Table |  |
|
| 39 | [SID103284478] | Unspecified | IC50 | 223 | Growth inhibition of BALB/c mouse cloned 3T3/A31 cells after 72 hrs by nigrosin assay [AID379089, Type: Literature] | |   View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Unspecified | | IC50 | 223 [uM] | | BioAssay | Growth inhibition of BALB/c mouse cloned 3T3/A31 cells after 72 hrs by nigrosin assay | | AID | 379089 | | BioAssay type | Literature | | Target | | | PubMed | 10096863 | | Data Table |  |
|
| 40 | [SID103284478] | Unspecified | IC50 | 2000 | Inhibition of bovine seminal microsomal COX1 assessed as PGE2 production preincubated for 10 mins [AID399404, Type: Literature] | Prostaglandin G/H synthase 1 [gi:166897622] |   View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Unspecified | | IC50 | 2000 [uM] | | BioAssay | Inhibition of bovine seminal microsomal COX1 assessed as PGE2 production preincubated for 10 mins | | AID | 399404 | | BioAssay type | Literature | | Target | Prostaglandin G/H synthase 1 [gi:166897622] | | PubMed | 9461646 | | Data Table |  |
|
| 41 | [SID103284478] | Unspecified | IC50 | 2000 | Inhibition of bovine seminal microsomal COX1 assessed as PGE2 production [AID399401, Type: Literature] | Prostaglandin G/H synthase 1 [gi:166897622] |   View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Unspecified | | IC50 | 2000 [uM] | | BioAssay | Inhibition of bovine seminal microsomal COX1 assessed as PGE2 production | | AID | 399401 | | BioAssay type | Literature | | Target | Prostaglandin G/H synthase 1 [gi:166897622] | | PubMed | 9461646 | | Data Table |  |
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| 42 | [SID103284478] | Unspecified | IC50 | 2000 | Inhibition of sheep placental cotyledons COX2 assessed as PGE2 production preincubated for 10 mins [AID399405, Type: Literature] | Prostaglandin G/H synthase 2 [gi:3914304] |   View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Unspecified | | IC50 | 2000 [uM] | | BioAssay | Inhibition of sheep placental cotyledons COX2 assessed as PGE2 production preincubated for 10 mins | | AID | 399405 | | BioAssay type | Literature | | Target | Prostaglandin G/H synthase 2 [gi:3914304] | | PubMed | 9461646 | | Data Table |  |
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| 43 | [SID103284478] | Unspecified | IC50 | 2000 | Inhibition of sheep placental cotyledons COX2 assessed as PGE2 production [AID399402, Type: Literature] | Prostaglandin G/H synthase 2 [gi:3914304] |   View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Unspecified | | IC50 | 2000 [uM] | | BioAssay | Inhibition of sheep placental cotyledons COX2 assessed as PGE2 production | | AID | 399402 | | BioAssay type | Literature | | Target | Prostaglandin G/H synthase 2 [gi:3914304] | | PubMed | 9461646 | | Data Table |  |
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| 44 | [SID103284478] | Unspecified | | | Displacement of [3H]DPCPX from adenosine A1 receptor in rat forebrain membrane assessed as fraction of receptor bound radioligand at 100 ug/mL [AID403918, Type: Literature] | Adenosine receptor A [gi:2827766] |   View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Unspecified | | BioAssay | Displacement of [3H]DPCPX from adenosine A1 receptor in rat forebrain membrane assessed as fraction of receptor bound radioligand at 100 ug/mL | | AID | 403918 | | BioAssay type | Literature | | Target | Adenosine receptor A [gi:2827766] | | PubMed | 9214739 | | Data Table |  |
|
| 45 | [SID85149171] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
|
| 46 | [SID85149171] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 85149171 | | CID | 5280459 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
|
| 47 | [SID103284478] | Unspecified | | | Stimulation of BALB/c mouse cloned 3T3/A31 cells growth at 0.01 to 1 ug/mL [AID379095, Type: Literature] | |   View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Unspecified | | BioAssay | Stimulation of BALB/c mouse cloned 3T3/A31 cells growth at 0.01 to 1 ug/mL | | AID | 379095 | | BioAssay type | Literature | | Target | | | PubMed | 10096863 | | Data Table |  |
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| 48 | [SID103284478] | Unspecified | | | ABTS radical scavenging activity assessed as trolox equivalent antioxidant capacity [AID456316, Type: Literature] | |   View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Unspecified | | BioAssay | ABTS radical scavenging activity assessed as trolox equivalent antioxidant capacity | | AID | 456316 | | BioAssay type | Literature | | Target | | | PubMed | 19944611 | | Data Table |  |
|
| 49 | [SID103284478] | Unspecified | | | Antioxidant activity assessed as trolox equivalent by TEAC assay [AID456317, Type: Literature] | |   View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Unspecified | | BioAssay | Antioxidant activity assessed as trolox equivalent by TEAC assay | | AID | 456317 | | BioAssay type | Literature | | Target | | | PubMed | 19944611 | | Data Table |  |
|
| 50 | [SID103284478] | Unspecified | | | DPPH radical scavenging activity assessed as trolox equivalent antioxidant capacity [AID456318, Type: Literature] | |   View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 103284478 | | CID | 5280459 | | Outcome | Unspecified | | BioAssay | DPPH radical scavenging activity assessed as trolox equivalent antioxidant capacity | | AID | 456318 | | BioAssay type | Literature | | Target | | | PubMed | 19944611 | | Data Table |  |
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