| 1 | [SID14738439] | Active | IC50 | 0.41394 | Homogeneous Time Resolved Fluorescence (HTRF)-based cell-based high throughput dose response assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID504701, Type: confirmatory] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | IC50 | 0.41394 [uM] | | BioAssay | Homogeneous Time Resolved Fluorescence (HTRF)-based cell-based high throughput dose response assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 504701 | | BioAssay type | confirmatory | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 2 | [SID14738439] | Active | IC50 | 0.41394 | Homogeneous Time Resolved Fluorescence (HTRF)-based cell-based high throughput dose response assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID504701, Type: confirmatory] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | IC50 | 0.41394 [uM] | | BioAssay | Homogeneous Time Resolved Fluorescence (HTRF)-based cell-based high throughput dose response assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 504701 | | BioAssay type | confirmatory | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 3 | [SID14738439] | Active | IC50 | 2.828 | Fluorescence-based cell-based high throughput dose response assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID504699, Type: confirmatory] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | IC50 | 2.828 [uM] | | BioAssay | Fluorescence-based cell-based high throughput dose response assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 504699 | | BioAssay type | confirmatory | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 4 | [SID14738439] | Active | IC50 | 2.828 | Fluorescence-based cell-based high throughput dose response assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID504699, Type: confirmatory] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | IC50 | 2.828 [uM] | | BioAssay | Fluorescence-based cell-based high throughput dose response assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 504699 | | BioAssay type | confirmatory | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
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| 5 | [SID14738439] | Active | Potency | 3.5481 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | Potency | 3.5481 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 6 | [SID14738439] | Active | IC50 | 3.81 | Dose Response confirmation of uHTS small molecule inhibitors of tim10-1: a luminescent TIM10 yeast counterscreen [AID504542, Type: confirmatory] | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | IC50 | 3.81 [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule inhibitors of tim10-1: a luminescent TIM10 yeast counterscreen | | AID | 504542 | | BioAssay type | confirmatory | | Target | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] | | PubMed | | | Data Table |  |
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| 7 | [SID14738439] | Active | IC50 | 8.03 | Dose Response confirmation of uHTS small molecule inhibitors of tim10-1 yeast via a luminescent assay [AID493003, Type: confirmatory] | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | IC50 | 8.03 [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule inhibitors of tim10-1 yeast via a luminescent assay | | AID | 493003 | | BioAssay type | confirmatory | | Target | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] | | PubMed | | | Data Table |  |
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| 8 | [SID14738439] | Active | IC50 | 9.86 | Dose Response confirmation of uHTS small molecule inhibitors of tim10-1: a luminescent tim23-1 yeast counterscreen. [AID504544, Type: confirmatory] | TPA: Tim23p [Saccharomyces cerevisiae S288c] [gi:285814664] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | IC50 | 9.86 [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule inhibitors of tim10-1: a luminescent tim23-1 yeast counterscreen. | | AID | 504544 | | BioAssay type | confirmatory | | Target | TPA: Tim23p [Saccharomyces cerevisiae S288c] [gi:285814664] | | PubMed | | | Data Table |  |
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| 9 | [SID14738439] | Active | Potency | 10 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 10 | [SID14738439] | Active | Potency | 12.5594 | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia [AID2451, Type: confirmatory] | Chain A, Structure Of Giardia Fructose-1,6-Biphosphate Aldolase In Complex With Phosphoglycolohydrox [gi:122920737] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | Potency | 12.5594 [uM] | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia | | AID | 2451 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Giardia Fructose-1,6-Biphosphate Aldolase In Complex With Phosphoglycolohydrox [gi:122920737] | | PubMed | | | Data Table |  |
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| 11 | [SID14738439] | Active | Potency | 28.1838 | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | Potency | 28.1838 [uM] | | BioAssay | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins | | AID | 485364 | | BioAssay type | confirmatory | | Target | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] | | PubMed | | | Data Table |  |
|
| 12 | [SID14738439] | Active | Potency | 31.6228 | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
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| 13 | [SID14738439] | Active | Potency | 31.6228 | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 14 | [SID14738439] | Active | Potency | 44.6684 | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a [AID504332, Type: confirmatory] | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | Potency | 44.6684 [uM] | | BioAssay | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a | | AID | 504332 | | BioAssay type | confirmatory | | Target | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] | | PubMed | | | Data Table |  |
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| 15 | [SID14738439] | Active | | | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen [AID2472, Type: screening] | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen | | AID | 2472 | | BioAssay type | screening | | Target | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] | | PubMed | | | Data Table |  |
|
| 16 | [SID14738439] | Active | | | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen [AID2472, Type: screening] | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen | | AID | 2472 | | BioAssay type | screening | | Target | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] | | PubMed | | | Data Table |  |
|
| 17 | [SID14738439] | Active | | | CYP2C19 Assay [AID778, Type: screening] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | CYP2C19 Assay | | AID | 778 | | BioAssay type | screening | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
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| 18 | [SID14738439] | Active | | | CYP2C19 Assay [AID778, Type: screening] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | CYP2C19 Assay | | AID | 778 | | BioAssay type | screening | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
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| 19 | [SID14738439] | Active | | | CYP2C9 Assay [AID777, Type: screening] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | CYP2C9 Assay | | AID | 777 | | BioAssay type | screening | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|
| 20 | [SID14738439] | Active | | | CYP2C9 Assay [AID777, Type: screening] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | CYP2C9 Assay | | AID | 777 | | BioAssay type | screening | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|
| 21 | [SID14738439] | Active | | | CYP2C9 Assay [AID777, Type: screening] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | CYP2C9 Assay | | AID | 777 | | BioAssay type | screening | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|
| 22 | [SID14738439] | Active | | | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID434989, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 434989 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 23 | [SID14738439] | Active | | | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID434989, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 434989 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 24 | [SID14738439] | Active | | | Fluorescence-based cell-based high throughput confirmation assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID492963, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Fluorescence-based cell-based high throughput confirmation assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 492963 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 25 | [SID14738439] | Active | | | Fluorescence-based cell-based high throughput confirmation assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID492963, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Fluorescence-based cell-based high throughput confirmation assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 492963 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 26 | [SID14738439] | Active | | | Homogeneous Time Resolved Fluorescence (HTRF)-based cell-based high throughput confirmation assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID492964, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Homogeneous Time Resolved Fluorescence (HTRF)-based cell-based high throughput confirmation assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 492964 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 27 | [SID14738439] | Active | | | Homogeneous Time Resolved Fluorescence (HTRF)-based cell-based high throughput confirmation assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID492964, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Homogeneous Time Resolved Fluorescence (HTRF)-based cell-based high throughput confirmation assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 492964 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 28 | [SID14738439] | Active | | | FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID485270, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 485270 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 29 | [SID14738439] | Active | | | FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID485270, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 485270 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 30 | [SID14738439] | Active | | | HTS identification of compounds inhibiting the binding of CD11b/CD18 to fibrinogen via a luminescence assay. [AID1497, Type: screening] | integrin alpha-M isoform 2 precursor [Homo sapiens] [gi:88501734] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | HTS identification of compounds inhibiting the binding of CD11b/CD18 to fibrinogen via a luminescence assay. | | AID | 1497 | | BioAssay type | screening | | Target | integrin alpha-M isoform 2 precursor [Homo sapiens] [gi:88501734] | | PubMed | | | Data Table |  |
|
| 31 | [SID14738439] | Active | | | HTS identification of compounds inhibiting the binding of CD11b/CD18 to fibrinogen via a luminescence assay. [AID1497, Type: screening] | integrin alpha-M isoform 2 precursor [Homo sapiens] [gi:88501734] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | HTS identification of compounds inhibiting the binding of CD11b/CD18 to fibrinogen via a luminescence assay. | | AID | 1497 | | BioAssay type | screening | | Target | integrin alpha-M isoform 2 precursor [Homo sapiens] [gi:88501734] | | PubMed | | | Data Table |  |
|
| 32 | [SID14738439] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists [AID624463, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | | AID | 624463 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 33 | [SID14738439] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists [AID624463, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | | AID | 624463 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 34 | [SID14738439] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists [AID624463, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | | AID | 624463 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 35 | [SID14738439] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists [AID624463, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | | AID | 624463 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 36 | [SID14738439] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists [AID624463, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | | AID | 624463 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 37 | [SID14738439] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators [AID624464, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | | AID | 624464 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 38 | [SID14738439] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators [AID624464, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | | AID | 624464 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
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| 39 | [SID14738439] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators [AID624464, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | | AID | 624464 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
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| 40 | [SID14738439] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators [AID624464, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | | AID | 624464 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
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| 41 | [SID14738439] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators [AID624464, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | | AID | 624464 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
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| 42 | [SID14738439] | Active | | | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the oxidoreductase glutathione S-transferase omega 1(GSTO1). [AID1974, Type: screening] | glutathione S-transferase omega-1 isoform 1 [Homo sapiens] [gi:4758484] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the oxidoreductase glutathione S-transferase omega 1(GSTO1). | | AID | 1974 | | BioAssay type | screening | | Target | glutathione S-transferase omega-1 isoform 1 [Homo sapiens] [gi:4758484] | | PubMed | | | Data Table |  |
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| 43 | [SID14738439] | Active | | | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the oxidoreductase glutathione S-transferase omega 1(GSTO1). [AID1974, Type: screening] | glutathione S-transferase omega-1 isoform 1 [Homo sapiens] [gi:4758484] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the oxidoreductase glutathione S-transferase omega 1(GSTO1). | | AID | 1974 | | BioAssay type | screening | | Target | glutathione S-transferase omega-1 isoform 1 [Homo sapiens] [gi:4758484] | | PubMed | | | Data Table |  |
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| 44 | [SID14738439] | Active | | | Single concentration confirmation of small molecule inhibitors of tim10-1 yeast via a luminescent assay [AID463213, Type: screening] | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | Single concentration confirmation of small molecule inhibitors of tim10-1 yeast via a luminescent assay | | AID | 463213 | | BioAssay type | screening | | Target | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] | | PubMed | | | Data Table |  |
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| 45 | [SID14738439] | Active | | | uHTS identification of small molecule inhibitors of tim10 yeast via a luminescent assay [AID463195, Type: screening] | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | uHTS identification of small molecule inhibitors of tim10 yeast via a luminescent assay | | AID | 463195 | | BioAssay type | screening | | Target | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] | | PubMed | | | Data Table |  |
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| 46 | [SID14738439] | Active | | | uHTS identification of small molecule inhibitors of tim10-1 yeast via a luminescent assay [AID463190, Type: screening] | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Active | | BioAssay | uHTS identification of small molecule inhibitors of tim10-1 yeast via a luminescent assay | | AID | 463190 | | BioAssay type | screening | | Target | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] | | PubMed | | | Data Table |  |
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| 47 | [SID14738439] | 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. | 47 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | 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 |  |
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| 48 | [SID14738439] | 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. | 48 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | 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 |  |
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| 49 | [SID14738439] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
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| 50 | [SID14738439] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 14738439 | | CID | 46499334 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
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