| 1 | [SID51088465] | Active | AC50 | 0.685 | Quorum LuxO: Assay for inducers of light production in the absence of#autoinducers using BH1651 (luxOD47E) Measured in Microorganism System Using Plate Reader - 2132-03_Agonist_Dose_CherryPick_Activity [AID624254, Type: confirmatory] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 51088465 | | CID | 3243472 | | Outcome | Active | | AC50 | 0.685 [uM] | | BioAssay | Quorum LuxO: Assay for inducers of light production in the absence of#autoinducers using BH1651 (luxOD47E) Measured in Microorganism System Using Plate Reader - 2132-03_Agonist_Dose_CherryPick_Activity | | AID | 624254 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 2 | [SID4249530] | Active | EC50 | 1.62 | Inhibitors of T-Type Calcium Channel [AID489005, Type: confirmatory] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | EC50 | 1.62 [uM] | | BioAssay | Inhibitors of T-Type Calcium Channel | | AID | 489005 | | BioAssay type | confirmatory | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
|
| 3 | [SID4249530] | Active | EC50 | 1.62 | Inhibitors of T-Type Calcium Channel [AID489005, Type: confirmatory] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | EC50 | 1.62 [uM] | | BioAssay | Inhibitors of T-Type Calcium Channel | | AID | 489005 | | BioAssay type | confirmatory | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
|
| 4 | [SID4249530] | Active | EC50 | 1.62 | Inhibitors of T-Type Calcium Channel [AID489005, Type: confirmatory] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | EC50 | 1.62 [uM] | | BioAssay | Inhibitors of T-Type Calcium Channel | | AID | 489005 | | BioAssay type | confirmatory | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
|
| 5 | [SID4249530] | Active | EC50 | 4.323 | Inhibitors of T-Type Calcium Channels [AID493021, Type: confirmatory] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | EC50 | 4.323 [uM] | | BioAssay | Inhibitors of T-Type Calcium Channels | | AID | 493021 | | BioAssay type | confirmatory | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
|
| 6 | [SID4249530] | Active | EC50 | 4.323 | Inhibitors of T-Type Calcium Channels [AID493021, Type: confirmatory] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | EC50 | 4.323 [uM] | | BioAssay | Inhibitors of T-Type Calcium Channels | | AID | 493021 | | BioAssay type | confirmatory | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
|
| 7 | [SID4249530] | Active | EC50 | 4.323 | Inhibitors of T-Type Calcium Channels [AID493021, Type: confirmatory] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | EC50 | 4.323 [uM] | | BioAssay | Inhibitors of T-Type Calcium Channels | | AID | 493021 | | BioAssay type | confirmatory | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
|
| 8 | [SID4249530] | Active | Potency | 23.1093 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | Potency | 23.1093 [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 | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 9 | [SID4249530] | Active | Potency | 23.1093 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | Potency | 23.1093 [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 | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 10 | [SID4249530] | Active | Potency | 23.1093 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | Potency | 23.1093 [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 | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 11 | [SID4249530] | Active | | | Primary cell-based high-throughput screening for identification of compounds that inhibit/block calcium-activated chloride channels (TMEM16A) [AID588511, Type: screening] | Ano1 gene product [Mus musculus] [gi:334278898] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that inhibit/block calcium-activated chloride channels (TMEM16A) | | AID | 588511 | | BioAssay type | screening | | Target | Ano1 gene product [Mus musculus] [gi:334278898] | | PubMed | | | Data Table |  |
|
| 12 | [SID92709275] | Active | | | Late stage assay provider results from the probe development effort to identify selective inhibitors of LYPLA2: Fluorescence-based biochemical gel-based ABPP inhibition [AID652029, Type: other] | LYPLA2 gene product [Homo sapiens] [gi:9966764] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 92709275 | | CID | 3243472 | | Outcome | Active | | BioAssay | Late stage assay provider results from the probe development effort to identify selective inhibitors of LYPLA2: Fluorescence-based biochemical gel-based ABPP inhibition | | AID | 652029 | | BioAssay type | other | | Target | LYPLA2 gene product [Homo sapiens] [gi:9966764] | | PubMed | | | Data Table |  |
|
| 13 | [SID4249530] | Active | | | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen [AID449739, Type: screening] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | BioAssay | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | | AID | 449739 | | BioAssay type | screening | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
|
| 14 | [SID4249530] | Active | | | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen [AID449739, Type: screening] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | BioAssay | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | | AID | 449739 | | BioAssay type | screening | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
|
| 15 | [SID4249530] | Active | | | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen [AID449739, Type: screening] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | BioAssay | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | | AID | 449739 | | BioAssay type | screening | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
|
| 16 | [SID51088465] | Active | | | HTS to identify compounds that promote myeloid differentiation with MLPCN compound set [AID624256, Type: screening] | |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 51088465 | | CID | 3243472 | | Outcome | Active | | BioAssay | HTS to identify compounds that promote myeloid differentiation with MLPCN compound set | | AID | 624256 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 17 | [SID4249530] | 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 | 4249530 | | CID | 3243472 | | 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 |  |
|
| 18 | [SID4249530] | 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 | 4249530 | | CID | 3243472 | | 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 |  |
|
| 19 | [SID4249530] | Active | | | HTS for Estrogen Receptor-beta Coactivator Binding inhibitors [AID633, Type: screening] | estrogen receptor beta isoform 1 [Homo sapiens] [gi:10835013] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | BioAssay | HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | | AID | 633 | | BioAssay type | screening | | Target | estrogen receptor beta isoform 1 [Homo sapiens] [gi:10835013] | | PubMed | | | Data Table |  |
|
| 20 | [SID4249530] | Active | | | HTS for Estrogen Receptor-beta Coactivator Binding inhibitors [AID633, Type: screening] | estrogen receptor beta isoform 1 [Homo sapiens] [gi:10835013] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | BioAssay | HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | | AID | 633 | | BioAssay type | screening | | Target | estrogen receptor beta isoform 1 [Homo sapiens] [gi:10835013] | | PubMed | | | Data Table |  |
|
| 21 | [SID4249530] | Active | | | HTS for Estrogen Receptor-beta Coactivator Binding inhibitors [AID633, Type: screening] | estrogen receptor beta isoform 1 [Homo sapiens] [gi:10835013] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | BioAssay | HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | | AID | 633 | | BioAssay type | screening | | Target | estrogen receptor beta isoform 1 [Homo sapiens] [gi:10835013] | | PubMed | | | Data Table |  |
|
| 22 | [SID51088465] | Active | | | Cholera Quorum: HTS for inducers of light production in the absence ofautoinducers using BH1578 (luxS deficient, cqsA deficient) Measured in Microorganism System Using Plate Reader - 2132-01_Agonist_SinglePoint_HTS_Activity [AID588436, Type: screening] | |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 51088465 | | CID | 3243472 | | Outcome | Active | | BioAssay | Cholera Quorum: HTS for inducers of light production in the absence ofautoinducers using BH1578 (luxS deficient, cqsA deficient) Measured in Microorganism System Using Plate Reader - 2132-01_Agonist_SinglePoint_HTS_Activity | | AID | 588436 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 23 | [SID4249530] | Active | | | Counterscreen for PME1 inhibitors: fluorescence polarization-based biochemical high throughput confirmation assay to identify inhibitors of lysophospholipase 2 (LYPLA2). [AID2232, Type: screening] | lysophospholipase II [Homo sapiens] [gi:4581413] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | BioAssay | Counterscreen for PME1 inhibitors: fluorescence polarization-based biochemical high throughput confirmation assay to identify inhibitors of lysophospholipase 2 (LYPLA2). | | AID | 2232 | | BioAssay type | screening | | Target | lysophospholipase II [Homo sapiens] [gi:4581413] | | PubMed | | | Data Table |  |
|
| 24 | [SID4249530] | Active | | | Counterscreen for PME1 inhibitors: fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of lysophospholipase 2 (LYPLA2). [AID2177, Type: screening] | lysophospholipase II [Homo sapiens] [gi:4581413] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Active | | BioAssay | Counterscreen for PME1 inhibitors: fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of lysophospholipase 2 (LYPLA2). | | AID | 2177 | | BioAssay type | screening | | Target | lysophospholipase II [Homo sapiens] [gi:4581413] | | PubMed | | | Data Table |  |
|
| 25 | [SID4249530] | Active | | | CYP2C9 Assay [AID777, Type: screening] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | 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 |  |
|
| 26 | [SID4249530] | Active | | | CYP2C9 Assay [AID777, Type: screening] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | 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 |  |
|
| 27 | [SID4249530] | Active | | | CYP2C9 Assay [AID777, Type: screening] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | 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 |  |
|
| 28 | [SID4249530] | 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. | 28 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | 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 |  |
|
| 29 | [SID4249530] | 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. | 29 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | 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 |  |
|
| 30 | [SID4249530] | 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. | 30 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | 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 |  |
|
| 31 | [SID4249530] | 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. | 31 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | 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 |  |
|
| 32 | [SID4249530] | 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. | 32 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | 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 |  |
|
| 33 | [SID81065456] | Inactive | EC50 | 1.919 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 wildtype [AID2037, Type: confirmatory] | cell division cycle 42 (GTP binding protein, 25kDa) [Homo sapiens] [gi:56202836] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 1.919 [uM] | | BioAssay | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 wildtype | | AID | 2037 | | BioAssay type | confirmatory | | Target | cell division cycle 42 (GTP binding protein, 25kDa) [Homo sapiens] [gi:56202836] | | PubMed | | | Data Table |  |
|
| 34 | [SID81065456] | Inactive | EC50 | 9.141 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 activated mutant [AID2051, Type: confirmatory] | Rac1 protein [Homo sapiens] [gi:8574038] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 9.141 [uM] | | BioAssay | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 activated mutant | | AID | 2051 | | BioAssay type | confirmatory | | Target | Rac1 protein [Homo sapiens] [gi:8574038] | | PubMed | | | Data Table |  |
|
| 35 | [SID81065456] | Inactive | EC50 | 9.141 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 activated mutant [AID2051, Type: confirmatory] | Rac1 protein [Homo sapiens] [gi:8574038] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 9.141 [uM] | | BioAssay | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 activated mutant | | AID | 2051 | | BioAssay type | confirmatory | | Target | Rac1 protein [Homo sapiens] [gi:8574038] | | PubMed | | | Data Table |  |
|
| 36 | [SID4249530] | Inactive | Potency | 12.5893 | qHTS for Activators of Integrin-Mediated Alleviation for Muscular Dystrophy [AID624291, Type: confirmatory] | Glycoprotein hormones alpha chain [gi:121312] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Inactive | | Potency | 12.5893 [uM] | | BioAssay | qHTS for Activators of Integrin-Mediated Alleviation for Muscular Dystrophy | | AID | 624291 | | BioAssay type | confirmatory | | Target | Glycoprotein hormones alpha chain [gi:121312] | | PubMed | | | Data Table |  |
|
| 37 | [SID4249530] | Inactive | Potency | 15.8489 | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium [AID1457, Type: confirmatory] | Inositol monophosphatase [gi:44888968] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Inactive | | Potency | 15.8489 [uM] | | BioAssay | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | | AID | 1457 | | BioAssay type | confirmatory | | Target | Inositol monophosphatase [gi:44888968] | | PubMed | | | Data Table |  |
|
| 38 | [SID4249530] | Inactive | Potency | 15.8489 | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium [AID1457, Type: confirmatory] | Inositol monophosphatase [gi:44888968] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Inactive | | Potency | 15.8489 [uM] | | BioAssay | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | | AID | 1457 | | BioAssay type | confirmatory | | Target | Inositol monophosphatase [gi:44888968] | | PubMed | | | Data Table |  |
|
| 39 | [SID4249530] | Inactive | Potency | 19.9526 | qHTS Assay for Inhibitors of Influenza NS1 Protein Function [AID2326, Type: confirmatory] | nonstructural protein 1 [Influenza A virus (A/WSN/1933(H1N1))] [gi:194352380] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 4249530 | | CID | 3243472 | | Outcome | Inactive | | Potency | 19.9526 [uM] | | BioAssay | qHTS Assay for Inhibitors of Influenza NS1 Protein Function | | AID | 2326 | | BioAssay type | confirmatory | | Target | nonstructural protein 1 [Influenza A virus (A/WSN/1933(H1N1))] [gi:194352380] | | PubMed | | | Data Table |  |
|
| 40 | [SID81065456] | Inactive | EC50 | 30 | Oxadiazole SAR compounds tested by Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 activated mutant [AID2009, Type: confirmatory] | cell division cycle 42 (GTP binding protein, 25kDa) [Homo sapiens] [gi:56202836] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 30 [uM] | | BioAssay | Oxadiazole SAR compounds tested by Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 activated mutant | | AID | 2009 | | BioAssay type | confirmatory | | Target | cell division cycle 42 (GTP binding protein, 25kDa) [Homo sapiens] [gi:56202836] | | PubMed | | | Data Table |  |
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| 41 | [SID81065456] | Inactive | EC50 | 30 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras activated mutant [AID2042, Type: confirmatory] | ras protein [Homo sapiens] [gi:190938] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 30 [uM] | | BioAssay | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras activated mutant | | AID | 2042 | | BioAssay type | confirmatory | | Target | ras protein [Homo sapiens] [gi:190938] | | PubMed | | | Data Table |  |
|
| 42 | [SID81065456] | Inactive | EC50 | 30 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras activated mutant [AID2042, Type: confirmatory] | ras protein [Homo sapiens] [gi:190938] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 30 [uM] | | BioAssay | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras activated mutant | | AID | 2042 | | BioAssay type | confirmatory | | Target | ras protein [Homo sapiens] [gi:190938] | | PubMed | | | Data Table |  |
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| 43 | [SID81065456] | Inactive | EC50 | 30 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras activated mutant [AID2042, Type: confirmatory] | ras protein [Homo sapiens] [gi:190938] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 30 [uM] | | BioAssay | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras activated mutant | | AID | 2042 | | BioAssay type | confirmatory | | Target | ras protein [Homo sapiens] [gi:190938] | | PubMed | | | Data Table |  |
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| 44 | [SID81065456] | Inactive | EC50 | 30 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype [AID2053, Type: confirmatory] | ras protein [Homo sapiens] [gi:190938] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 30 [uM] | | BioAssay | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | | AID | 2053 | | BioAssay type | confirmatory | | Target | ras protein [Homo sapiens] [gi:190938] | | PubMed | | | Data Table |  |
|
| 45 | [SID81065456] | Inactive | EC50 | 30 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype [AID2053, Type: confirmatory] | ras protein [Homo sapiens] [gi:190938] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 30 [uM] | | BioAssay | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | | AID | 2053 | | BioAssay type | confirmatory | | Target | ras protein [Homo sapiens] [gi:190938] | | PubMed | | | Data Table |  |
|
| 46 | [SID81065456] | Inactive | EC50 | 30 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype [AID2053, Type: confirmatory] | ras protein [Homo sapiens] [gi:190938] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 30 [uM] | | BioAssay | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | | AID | 2053 | | BioAssay type | confirmatory | | Target | ras protein [Homo sapiens] [gi:190938] | | PubMed | | | Data Table |  |
|
| 47 | [SID81065456] | Inactive | EC50 | 30 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab2 wildtype [AID2033, Type: confirmatory] | Ras-related protein Rab-2 [gi:46577642] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 30 [uM] | | BioAssay | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab2 wildtype | | AID | 2033 | | BioAssay type | confirmatory | | Target | Ras-related protein Rab-2 [gi:46577642] | | PubMed | | | Data Table |  |
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| 48 | [SID81065456] | Inactive | EC50 | 30 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab7 wildtype [AID2031, Type: confirmatory] | GTP-binding protein (rab7) [Canis lupus familiaris] [gi:164058] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 30 [uM] | | BioAssay | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab7 wildtype | | AID | 2031 | | BioAssay type | confirmatory | | Target | GTP-binding protein (rab7) [Canis lupus familiaris] [gi:164058] | | PubMed | | | Data Table |  |
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| 49 | [SID81065456] | Inactive | EC50 | 30 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 wildtype [AID2027, Type: confirmatory] | Rac1 protein [Homo sapiens] [gi:8574038] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 30 [uM] | | BioAssay | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 wildtype | | AID | 2027 | | BioAssay type | confirmatory | | Target | Rac1 protein [Homo sapiens] [gi:8574038] | | PubMed | | | Data Table |  |
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| 50 | [SID81065456] | Inactive | EC50 | 30 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 wildtype [AID2027, Type: confirmatory] | Rac1 protein [Homo sapiens] [gi:8574038] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 81065456 | | CID | 3243472 | | Outcome | Inactive | | EC50 | 30 [uM] | | BioAssay | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 wildtype | | AID | 2027 | | BioAssay type | confirmatory | | Target | Rac1 protein [Homo sapiens] [gi:8574038] | | PubMed | | | Data Table |  |
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