| 1 | [SID11532927] | Active | Potency | 0.5012 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 0.5012 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
|
| 2 | [SID11532927] | Active | Potency | 0.5012 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 0.5012 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
|
| 3 | [SID11532927] | Active | Potency | 0.7079 | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) [AID485290, Type: confirmatory] | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 0.7079 [uM] | | BioAssay | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) | | AID | 485290 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] | | PubMed | | | Data Table |  |
|
| 4 | [SID11532927] | Active | Potency | 1.2589 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 1.2589 [uM] | | BioAssay | qHTS Assay for Inhibitors of BAZ2B | | AID | 504333 | | BioAssay type | confirmatory | | Target | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] | | PubMed | | | Data Table |  |
|
| 5 | [SID11532927] | Active | Potency | 2.5119 | qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) [AID2517, Type: confirmatory] | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 2.5119 [uM] | | BioAssay | qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) | | AID | 2517 | | BioAssay type | confirmatory | | Target | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] | | PubMed | | | Data Table |  |
|
| 6 | [SID11532927] | Active | Potency | 3.1623 | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) [AID2549, Type: confirmatory] | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) | | AID | 2549 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] | | PubMed | | | Data Table |  |
|
| 7 | [SID11532927] | Active | Potency | 3.1623 | 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. | 7 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 3.1623 [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 |  |
|
| 8 | [SID11532927] | Active | EC50 | 4.35 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao. [AID1871, Type: confirmatory] | RGS7 [Homo sapiens] [gi:1166512] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | EC50 | 4.35 [uM] | | BioAssay | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao. | | AID | 1871 | | BioAssay type | confirmatory | | Target | RGS7 [Homo sapiens] [gi:1166512] | | PubMed | | | Data Table |  |
|
| 9 | [SID11532927] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 10 | [SID11532927] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 11 | [SID11532927] | Active | EC50 | 7.31 | Dose respone, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. [AID1888, Type: confirmatory] | regulator of G-protein signaling 16 [Homo sapiens] [gi:156416009] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | EC50 | 7.31 [uM] | | BioAssay | Dose respone, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. | | AID | 1888 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 16 [Homo sapiens] [gi:156416009] | | PubMed | | | Data Table |  |
|
| 12 | [SID11532927] | Active | EC50 | 7.53 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao. [AID1884, Type: confirmatory] | regulator of G-protein signaling 19 [Homo sapiens] [gi:86990435] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | EC50 | 7.53 [uM] | | BioAssay | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao. | | AID | 1884 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 19 [Homo sapiens] [gi:86990435] | | PubMed | | | Data Table |  |
|
| 13 | [SID11532927] | Active | Potency | 7.9433 | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 7.9433 [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 |  |
|
| 14 | [SID11532927] | Active | EC50 | 11.75 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. [AID1872, Type: confirmatory] | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301151] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | EC50 | 11.75 [uM] | | BioAssay | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | | AID | 1872 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301151] | | PubMed | | | Data Table |  |
|
| 15 | [SID11532927] | Active | EC50 | 11.75 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. [AID1872, Type: confirmatory] | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301151] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | EC50 | 11.75 [uM] | | BioAssay | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | | AID | 1872 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301151] | | PubMed | | | Data Table |  |
|
| 16 | [SID11532927] | Active | EC50 | 11.75 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. [AID1872, Type: confirmatory] | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301151] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | EC50 | 11.75 [uM] | | BioAssay | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | | AID | 1872 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301151] | | PubMed | | | Data Table |  |
|
| 17 | [SID11532927] | Active | IC50 | 12.35 | Dose Response Confirmation for Small Molecule Inhibitors of Eukaryotic Translation Initiation [AID855, Type: confirmatory] | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | IC50 | 12.35 [uM] | | BioAssay | Dose Response Confirmation for Small Molecule Inhibitors of Eukaryotic Translation Initiation | | AID | 855 | | BioAssay type | confirmatory | | Target | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] | | PubMed | | | Data Table |  |
|
| 18 | [SID11532927] | Active | IC50 | 12.35 | Dose Response Confirmation for Small Molecule Inhibitors of Eukaryotic Translation Initiation [AID855, Type: confirmatory] | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | IC50 | 12.35 [uM] | | BioAssay | Dose Response Confirmation for Small Molecule Inhibitors of Eukaryotic Translation Initiation | | AID | 855 | | BioAssay type | confirmatory | | Target | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] | | PubMed | | | Data Table |  |
|
| 19 | [SID11532927] | Active | Potency | 14.1254 | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) [AID2528, Type: confirmatory] | Bloom syndrome protein [Homo sapiens] [gi:4557365] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 14.1254 [uM] | | BioAssay | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) | | AID | 2528 | | BioAssay type | confirmatory | | Target | Bloom syndrome protein [Homo sapiens] [gi:4557365] | | PubMed | | | Data Table |  |
|
| 20 | [SID11532927] | Active | Potency | 14.1254 | 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. | 20 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 14.1254 [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 |  |
|
| 21 | [SID11532927] | Active | Potency | 14.1254 | 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. | 21 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 14.1254 [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 |  |
|
| 22 | [SID11532927] | Active | Potency | 50.1187 | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) [AID1490, Type: confirmatory] | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | Potency | 50.1187 [uM] | | BioAssay | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) | | AID | 1490 | | BioAssay type | confirmatory | | Target | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] | | PubMed | | | Data Table |  |
|
| 23 | [SID11532927] | Active | | | Epi-absorbance primary biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase [AID1556, Type: screening] | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | Epi-absorbance primary biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase | | AID | 1556 | | BioAssay type | screening | | Target | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] | | PubMed | | | Data Table |  |
|
| 24 | [SID11532927] | Active | IC50 | | uHTS fluorescence assay for the identification of Human Immunodeficiency Virus Fusion Inhibitors. [AID1986, Type: confirmatory] | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | IC50 | [uM] | | BioAssay | uHTS fluorescence assay for the identification of Human Immunodeficiency Virus Fusion Inhibitors. | | AID | 1986 | | BioAssay type | confirmatory | | Target | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] | | PubMed | | | Data Table |  |
|
| 25 | [SID11532927] | Active | | | HTS to Find Inhibitors of Pathogenic Pemphigus Antibodies from validation set [AID588368, Type: screening] | |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | HTS to Find Inhibitors of Pathogenic Pemphigus Antibodies from validation set | | AID | 588368 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 26 | [SID11532927] | Active | | | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of the Hepatitis C Virus non-structural protein 3 helicase (NS3) [AID1800, Type: screening] | NS3 [Hepatitis C virus] [gi:125541954] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of the Hepatitis C Virus non-structural protein 3 helicase (NS3) | | AID | 1800 | | BioAssay type | screening | | Target | NS3 [Hepatitis C virus] [gi:125541954] | | PubMed | | | Data Table |  |
|
| 27 | [SID11532927] | Active | | | RNA aptamer-based validation for inhibitors of GRK2 [AID488806, Type: screening] | beta-adrenergic receptor kinase 1 [Homo sapiens] [gi:148539876] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | RNA aptamer-based validation for inhibitors of GRK2 | | AID | 488806 | | BioAssay type | screening | | Target | beta-adrenergic receptor kinase 1 [Homo sapiens] [gi:148539876] | | PubMed | | | Data Table |  |
|
| 28 | [SID10321954] | Active | | | MDR-1 [AID377, Type: other] | ABCB1 gene product [Homo sapiens] [gi:42741659] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 10321954 | | CID | 54679406 | | Outcome | Active | | BioAssay | MDR-1 | | AID | 377 | | BioAssay type | other | | Target | ABCB1 gene product [Homo sapiens] [gi:42741659] | | PubMed | | | Data Table |  |
|
| 29 | [SID10321954] | Active | | | MDR-1 [AID377, Type: other] | ABCB1 gene product [Homo sapiens] [gi:42741659] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 10321954 | | CID | 54679406 | | Outcome | Active | | BioAssay | MDR-1 | | AID | 377 | | BioAssay type | other | | Target | ABCB1 gene product [Homo sapiens] [gi:42741659] | | PubMed | | | Data Table |  |
|
| 30 | [SID10321954] | Active | | | MDR-1 [AID377, Type: other] | ABCB1 gene product [Homo sapiens] [gi:42741659] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 10321954 | | CID | 54679406 | | Outcome | Active | | BioAssay | MDR-1 | | AID | 377 | | BioAssay type | other | | Target | ABCB1 gene product [Homo sapiens] [gi:42741659] | | PubMed | | | Data Table |  |
|
| 31 | [SID11532927] | Active | | | uHTS of Mcl-1/Bid interaction inhibitors [AID1021, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Bid interaction inhibitors | | AID | 1021 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 32 | [SID11532927] | Active | | | uHTS of Mcl-1/Bid interaction inhibitors [AID1021, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Bid interaction inhibitors | | AID | 1021 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 33 | [SID11532927] | Active | | | uHTS of Mcl-1/Bid interaction inhibitors [AID1021, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Bid interaction inhibitors | | AID | 1021 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 34 | [SID11532927] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 35 | [SID11532927] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 36 | [SID11532927] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 37 | [SID11532927] | Active | | | Assay for Inhibitors of the beta-Arrestin-Adaptor Protein 2 Interaction for Validation Set [AID504541, Type: screening] | Arrestin, beta 1 [Homo sapiens] [gi:13177715] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | Assay for Inhibitors of the beta-Arrestin-Adaptor Protein 2 Interaction for Validation Set | | AID | 504541 | | BioAssay type | screening | | Target | Arrestin, beta 1 [Homo sapiens] [gi:13177715] | | PubMed | | | Data Table |  |
|
| 38 | [SID11532927] | 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. | 38 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | 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 |  |
|
| 39 | [SID11532927] | 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. | 39 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | 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 |  |
|
| 40 | [SID11532927] | Active | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. [AID1423, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | | AID | 1423 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 41 | [SID11532927] | Active | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. [AID1423, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | | AID | 1423 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 42 | [SID11532927] | Active | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. [AID1423, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | | AID | 1423 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 43 | [SID11532927] | Active | | | 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. | 43 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | 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 |  |
|
| 44 | [SID11532927] | Active | | | 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. | 44 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | 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 |  |
|
| 45 | [SID11532927] | Active | | | 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. | 45 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | 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 |  |
|
| 46 | [SID11532927] | Active | | | Single point concentration, multiplexed high-throughput screen for confirmation of small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. [AID1836, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | Single point concentration, multiplexed high-throughput screen for confirmation of small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | | AID | 1836 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 47 | [SID11532927] | Active | | | Single point concentration, multiplexed high-throughput screen for confirmation of small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. [AID1836, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | Single point concentration, multiplexed high-throughput screen for confirmation of small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | | AID | 1836 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 48 | [SID11532927] | Active | | | Single point concentration, multiplexed high-throughput screen for confirmation of small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. [AID1836, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | Single point concentration, multiplexed high-throughput screen for confirmation of small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | | AID | 1836 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 49 | [SID11532927] | Active | | | Single point concentration, multiplexed high-throughput screen for confirmation of small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. [AID1838, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | Single point concentration, multiplexed high-throughput screen for confirmation of small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. | | AID | 1838 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 50 | [SID11532927] | Active | | | Single point concentration, multiplexed high-throughput screen for confirmation of small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. [AID1838, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 11532927 | | CID | 54679406 | | Outcome | Active | | BioAssay | Single point concentration, multiplexed high-throughput screen for confirmation of small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. | | AID | 1838 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|