| 1 | [SID855842] | Active | | | Aqueous Solubility from MLSMR Stock Solutions [AID1996, Type: other] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Active | | BioAssay | Aqueous Solubility from MLSMR Stock Solutions | | AID | 1996 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 2 | [SID855842] | Active | | | HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists [AID485358, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | | AID | 485358 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 3 | [SID855842] | Active | | | HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists [AID485358, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | | AID | 485358 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 4 | [SID855842] | Active | | | HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists [AID485358, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | | AID | 485358 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 5 | [SID855842] | Active | | | HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists [AID485358, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | | AID | 485358 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 6 | [SID855842] | Active | | | HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists [AID485358, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | | AID | 485358 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 7 | [SID855842] | Active | | | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists [AID485344, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | | AID | 485344 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 8 | [SID855842] | Active | | | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists [AID485344, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | | AID | 485344 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 9 | [SID855842] | Active | | | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists [AID485344, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | | AID | 485344 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 10 | [SID855842] | Active | | | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists [AID485344, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | | AID | 485344 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 11 | [SID855842] | Active | | | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists [AID485344, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | | AID | 485344 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 12 | [SID10321630] | Active | | | MDR-1 [AID377, Type: other] | ABCB1 gene product [Homo sapiens] [gi:42741659] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 10321630 | | CID | 3169 | | Outcome | Active | | BioAssay | MDR-1 | | AID | 377 | | BioAssay type | other | | Target | ABCB1 gene product [Homo sapiens] [gi:42741659] | | PubMed | | | Data Table |  |
|
| 13 | [SID10321630] | Active | | | MDR-1 [AID377, Type: other] | ABCB1 gene product [Homo sapiens] [gi:42741659] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 10321630 | | CID | 3169 | | Outcome | Active | | BioAssay | MDR-1 | | AID | 377 | | BioAssay type | other | | Target | ABCB1 gene product [Homo sapiens] [gi:42741659] | | PubMed | | | Data Table |  |
|
| 14 | [SID10321630] | Active | | | MDR-1 [AID377, Type: other] | ABCB1 gene product [Homo sapiens] [gi:42741659] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 10321630 | | CID | 3169 | | Outcome | Active | | BioAssay | MDR-1 | | AID | 377 | | BioAssay type | other | | Target | ABCB1 gene product [Homo sapiens] [gi:42741659] | | PubMed | | | Data Table |  |
|
| 15 | [SID56422462] | Active | | | HTS to identify compounds that promote myeloid differentiation with MLPCN compound set [AID624256, Type: screening] | |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 56422462 | | CID | 3169 | | Outcome | Active | | BioAssay | HTS to identify compounds that promote myeloid differentiation with MLPCN compound set | | AID | 624256 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 16 | [SID104171374] | Unspecified | | | qHTS profiling for inhibitors of Plasmodium falciparum proliferation [AID504749, Type: Literature] | |   View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 104171374 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | qHTS profiling for inhibitors of Plasmodium falciparum proliferation | | AID | 504749 | | BioAssay type | Literature | | Target | | | PubMed | 21817045 | | Data Table |  |
|
| 17 | [SID103395114] | Unspecified | | | Antitussive activity by inhibition of irritant citric acid aerosol-induced coughing in guinea pig upon oral administration. [AID74202, Type: Literature] | |   View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 103395114 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | Antitussive activity by inhibition of irritant citric acid aerosol-induced coughing in guinea pig upon oral administration. | | AID | 74202 | | BioAssay type | Literature | | Target | | | PubMed | 7853344 | | Data Table |  |
|
| 18 | [SID103395114] | Unspecified | | | Inhibition of irritant electrically-induced coughing in guinea pig trachea following p.o. administration. [AID74204, Type: Literature] | |   View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 103395114 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | Inhibition of irritant electrically-induced coughing in guinea pig trachea following p.o. administration. | | AID | 74204 | | BioAssay type | Literature | | Target | | | PubMed | 7853344 | | Data Table |  |
|
| 19 | [SID56422462] | 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. | 19 | | Structure |
| | Substance | | | SID | 56422462 | | CID | 3169 | | 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 |  |
|
| 20 | [SID56422462] | 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. | 20 | | Structure |
| | Substance | | | SID | 56422462 | | CID | 3169 | | 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 |  |
|
| 21 | [SID26747219] | Unspecified | | | qHTS profiling for inhibitors of Plasmodium falciparum proliferation [AID504749, Type: Literature] | |   View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 26747219 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | qHTS profiling for inhibitors of Plasmodium falciparum proliferation | | AID | 504749 | | BioAssay type | Literature | | Target | | | PubMed | 21817045 | | Data Table |  |
|
| 22 | [SID8149692] | Unspecified | | | Assay to identify inhibitors of polyglutamine-induced caspase-3 activation (CASP3) [AID1583, Type: other] | |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 8149692 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | Assay to identify inhibitors of polyglutamine-induced caspase-3 activation (CASP3) | | AID | 1583 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 23 | [SID8149692] | Unspecified | | | Yeast cell-based screen for compounds that suppress polyglutamine aggregation in vivo (75Q-TubU) [AID1593, Type: other] | |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 8149692 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | Yeast cell-based screen for compounds that suppress polyglutamine aggregation in vivo (75Q-TubU) | | AID | 1593 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 24 | [SID8149692] | Unspecified | | | Screen for compounds that correct neuronal dysfunction without cell death as induced by the expression of polyglutamine-expanded, N-terminal huntingtin in C. elegans mechanosensory neurons (HDELENEU) [AID1599, Type: other] | |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 8149692 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | Screen for compounds that correct neuronal dysfunction without cell death as induced by the expression of polyglutamine-expanded, N-terminal huntingtin in C. elegans mechanosensory neurons (HDELENEU) | | AID | 1599 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 25 | [SID8149692] | Unspecified | | | Screen for compounds that selectively inhibit cytochrome c release from purified mitochondria (CytoCRel) [AID1603, Type: other] | |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 8149692 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | Screen for compounds that selectively inhibit cytochrome c release from purified mitochondria (CytoCRel) | | AID | 1603 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 26 | [SID8149692] | Unspecified | | | Screen for compounds that inhibit polyglutamine induced protein aggregation (AGREG) [AID1604, Type: other] | |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 8149692 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | Screen for compounds that inhibit polyglutamine induced protein aggregation (AGREG) | | AID | 1604 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 27 | [SID8149692] | Unspecified | | | Screening of compounds showing protective effect against cell death induced by familial amyotrophic lateral sclerosis (FALS)-linked mutantsuperoxide dismutase 1 (SOD1) (ALSOD1) [AID1605, Type: other] | |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 8149692 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | Screening of compounds showing protective effect against cell death induced by familial amyotrophic lateral sclerosis (FALS)-linked mutantsuperoxide dismutase 1 (SOD1) (ALSOD1) | | AID | 1605 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 28 | [SID8149692] | Unspecified | | | Screen for compounds that induce the human heat shock transcriptional response (HSEluc) [AID1611, Type: other] | |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 8149692 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | Screen for compounds that induce the human heat shock transcriptional response (HSEluc) | | AID | 1611 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 29 | [SID8149692] | Unspecified | | | Screen for compounds that increase glutamate transport activity in MN-1 cell line (GluUPTAKE) [AID1612, Type: other] | |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 8149692 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | Screen for compounds that increase glutamate transport activity in MN-1 cell line (GluUPTAKE) | | AID | 1612 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 30 | [SID8149692] | Unspecified | | | Screen for compounds that inhibit protein aggregation formed by mutant SOD1 (GFPSOD1) [AID1613, Type: other] | |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 8149692 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | Screen for compounds that inhibit protein aggregation formed by mutant SOD1 (GFPSOD1) | | AID | 1613 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 31 | [SID8149692] | Unspecified | | | Screen for compounds that reduce polyglutamine (polyQ) inclusions in nerve growth factor (NGF)-treated PC12 cells (GFPQ80) [AID1614, Type: other] | |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 8149692 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | Screen for compounds that reduce polyglutamine (polyQ) inclusions in nerve growth factor (NGF)-treated PC12 cells (GFPQ80) | | AID | 1614 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 32 | [SID8149692] | Unspecified | | | Yeast cell-based screen for compounds that suppress polyglutamine aggregation in vivo (75Q-TubH) [AID1616, Type: other] | |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 8149692 | | CID | 3169 | | Outcome | Unspecified | | BioAssay | Yeast cell-based screen for compounds that suppress polyglutamine aggregation in vivo (75Q-TubH) | | AID | 1616 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 33 | [SID104171374] | Inactive | Potency | 15.8489 | qHTS for Inhibitors of Glutaminase (GLS) [AID624170, Type: confirmatory] | GLS protein [Homo sapiens] [gi:71051501] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 104171374 | | CID | 3169 | | Outcome | Inactive | | Potency | 15.8489 [uM] | | BioAssay | qHTS for Inhibitors of Glutaminase (GLS) | | AID | 624170 | | BioAssay type | confirmatory | | Target | GLS protein [Homo sapiens] [gi:71051501] | | PubMed | | | Data Table |  |
|
| 34 | [SID56422462] | Inactive | Potency | 35.4813 | qHTS for Inhibitors of Glutaminase (GLS) [AID624170, Type: confirmatory] | GLS protein [Homo sapiens] [gi:71051501] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 56422462 | | CID | 3169 | | Outcome | Inactive | | Potency | 35.4813 [uM] | | BioAssay | qHTS for Inhibitors of Glutaminase (GLS) | | AID | 624170 | | BioAssay type | confirmatory | | Target | GLS protein [Homo sapiens] [gi:71051501] | | PubMed | | | Data Table |  |
|
| 35 | [SID855842] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. [AID1415, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | | AID | 1415 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 36 | [SID855842] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. [AID1415, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | | AID | 1415 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 37 | [SID855842] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. [AID1415, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | | AID | 1415 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 38 | [SID56422462] | Inactive | Potency | | qHTS of GLP-1 Receptor Inverse Agonists: Cytotox Screen [AID624418, Type: confirmatory] | |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 56422462 | | CID | 3169 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS of GLP-1 Receptor Inverse Agonists: Cytotox Screen | | AID | 624418 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 39 | [SID56422462] | Inactive | | | Counterscreen of compound fluorescence effects on High-throughput multiplex microsphere screening for inhibitors of toxin protease [AID624483, Type: screening] | |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 56422462 | | CID | 3169 | | Outcome | Inactive | | BioAssay | Counterscreen of compound fluorescence effects on High-throughput multiplex microsphere screening for inhibitors of toxin protease | | AID | 624483 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 40 | [SID85788460] | Inactive | | | Fluorescence Cell-Based Primary HTS to Identify Reactive Oxygen Species Inducers in Cancer Cells Measured in Cell-Based System Using Plate Reader and Imaging Combination - 2044-01_Activator_SinglePoint_HTS_Activity [AID624156, Type: screening] | |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 85788460 | | CID | 3169 | | Outcome | Inactive | | BioAssay | Fluorescence Cell-Based Primary HTS to Identify Reactive Oxygen Species Inducers in Cancer Cells Measured in Cell-Based System Using Plate Reader and Imaging Combination - 2044-01_Activator_SinglePoint_HTS_Activity | | AID | 624156 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 41 | [SID92124271] | Inactive | | | A screen for compounds that inhibit liver stage malaria [AID624349, Type: other] | |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 92124271 | | CID | 3169 | | Outcome | Inactive | | BioAssay | A screen for compounds that inhibit liver stage malaria | | AID | 624349 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 42 | [SID103914118] | Inactive | | | Screening small molecules to find regulators of human embryonic stem cell survival. [AID493140, Type: screening] | |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 103914118 | | CID | 3169 | | Outcome | Inactive | | BioAssay | Screening small molecules to find regulators of human embryonic stem cell survival. | | AID | 493140 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 43 | [SID855842] | Inactive | Potency | | qHTS Assay for Lipid Storage Modulators in Drosophila S3 Cells [AID2685, Type: confirmatory] | |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Lipid Storage Modulators in Drosophila S3 Cells | | AID | 2685 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 44 | [SID855842] | Inactive | | | A yeast HTS for caloric restriction mimetics that inhibit age-related superoxide for Validation Compound Set [AID2706, Type: screening] | |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Inactive | | BioAssay | A yeast HTS for caloric restriction mimetics that inhibit age-related superoxide for Validation Compound Set | | AID | 2706 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 45 | [SID855842] | Inactive | | | uHTS luminescence assay for the identification of chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation [AID435003, Type: screening] | |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Inactive | | BioAssay | uHTS luminescence assay for the identification of chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation | | AID | 435003 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 46 | [SID855842] | Inactive | | | uHTS luminescence assay for the identification of chemical inhibitors of B-cell specific antigen receptor-induced NF-kB activation [AID435022, Type: screening] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Inactive | | BioAssay | uHTS luminescence assay for the identification of chemical inhibitors of B-cell specific antigen receptor-induced NF-kB activation | | AID | 435022 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 47 | [SID855842] | Inactive | | | uHTS identification of small molecule activators of the apoptotic arm of the Unfolded Protein response via a luminescent-based reporter assay [AID449763, Type: screening] | |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 855842 | | CID | 3169 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule activators of the apoptotic arm of the Unfolded Protein response via a luminescent-based reporter assay | | AID | 449763 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 48 | [SID26747219] | Inactive | Potency | | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1463, Type: confirmatory] | |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 26747219 | | CID | 3169 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1463 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 49 | [SID26747219] | Inactive | Potency | | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia [AID1477, Type: confirmatory] | |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 26747219 | | CID | 3169 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia | | AID | 1477 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 50 | [SID26747219] | Inactive | Potency | | qHTS Assay for Lipid Storage Modulators [AID1519, Type: confirmatory] | |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 26747219 | | CID | 3169 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Lipid Storage Modulators | | AID | 1519 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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