| 1 | [SID103188158] | Active | IC50 | 0.017 | Compound was tested for the inhibition of [3H]ketanserin binding to 5-hydroxytryptamine 2A receptor [AID5482, Type: Literature] | |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.017 [uM] | | BioAssay | Compound was tested for the inhibition of [3H]ketanserin binding to 5-hydroxytryptamine 2A receptor | | AID | 5482 | | BioAssay type | Literature | | Target | | | PubMed | 9986703 | | Data Table |  |
|
| 2 | [SID103188158] | Active | IC50 | 0.02 | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2A radioligand binding (ligand: [3H] Ketanserin) [AID625192, Type: other] | 5-hydroxytryptamine receptor 2A [gi:543727] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.02 [uM] | | BioAssay | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2A radioligand binding (ligand: [3H] Ketanserin) | | AID | 625192 | | BioAssay type | other | | Target | 5-hydroxytryptamine receptor 2A [gi:543727] | | PubMed | | | Data Table |  |
|
| 3 | [SID103188158] | Active | IC50 | 0.02 | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2A radioligand binding (ligand: [3H] Ketanserin) [AID625192, Type: other] | 5-hydroxytryptamine receptor 2A [gi:543727] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.02 [uM] | | BioAssay | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2A radioligand binding (ligand: [3H] Ketanserin) | | AID | 625192 | | BioAssay type | other | | Target | 5-hydroxytryptamine receptor 2A [gi:543727] | | PubMed | | | Data Table |  |
|
| 4 | [SID103188158] | Active | IC50 | 0.02 | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2A radioligand binding (ligand: [3H] Ketanserin) [AID625192, Type: other] | 5-hydroxytryptamine receptor 2A [gi:543727] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.02 [uM] | | BioAssay | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2A radioligand binding (ligand: [3H] Ketanserin) | | AID | 625192 | | BioAssay type | other | | Target | 5-hydroxytryptamine receptor 2A [gi:543727] | | PubMed | | | Data Table |  |
|
| 5 | [SID103188158] | Active | IC50 | 0.091 | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2C radioligand binding (ligand: [3H] Mesulergine) [AID625218, Type: other] | 5-hydroxytryptamine receptor 2C [gi:112816] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.091 [uM] | | BioAssay | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2C radioligand binding (ligand: [3H] Mesulergine) | | AID | 625218 | | BioAssay type | other | | Target | 5-hydroxytryptamine receptor 2C [gi:112816] | | PubMed | | | Data Table |  |
|
| 6 | [SID103188158] | Active | IC50 | 0.091 | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2C radioligand binding (ligand: [3H] Mesulergine) [AID625218, Type: other] | 5-hydroxytryptamine receptor 2C [gi:112816] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.091 [uM] | | BioAssay | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2C radioligand binding (ligand: [3H] Mesulergine) | | AID | 625218 | | BioAssay type | other | | Target | 5-hydroxytryptamine receptor 2C [gi:112816] | | PubMed | | | Data Table |  |
|
| 7 | [SID103188158] | Active | IC50 | 0.091 | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2C radioligand binding (ligand: [3H] Mesulergine) [AID625218, Type: other] | 5-hydroxytryptamine receptor 2C [gi:112816] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.091 [uM] | | BioAssay | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2C radioligand binding (ligand: [3H] Mesulergine) | | AID | 625218 | | BioAssay type | other | | Target | 5-hydroxytryptamine receptor 2C [gi:112816] | | PubMed | | | Data Table |  |
|
| 8 | [SID103188158] | Active | IC50 | 0.107 | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2B radioligand binding (ligand: [3H] Lysergic acid diethylamide) [AID625217, Type: other] | 5-hydroxytryptamine receptor 2B [gi:1168220] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.107 [uM] | | BioAssay | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2B radioligand binding (ligand: [3H] Lysergic acid diethylamide) | | AID | 625217 | | BioAssay type | other | | Target | 5-hydroxytryptamine receptor 2B [gi:1168220] | | PubMed | | | Data Table |  |
|
| 9 | [SID103188158] | Active | IC50 | 0.107 | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2B radioligand binding (ligand: [3H] Lysergic acid diethylamide) [AID625217, Type: other] | 5-hydroxytryptamine receptor 2B [gi:1168220] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.107 [uM] | | BioAssay | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2B radioligand binding (ligand: [3H] Lysergic acid diethylamide) | | AID | 625217 | | BioAssay type | other | | Target | 5-hydroxytryptamine receptor 2B [gi:1168220] | | PubMed | | | Data Table |  |
|
| 10 | [SID103188158] | Active | IC50 | 0.107 | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2B radioligand binding (ligand: [3H] Lysergic acid diethylamide) [AID625217, Type: other] | 5-hydroxytryptamine receptor 2B [gi:1168220] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.107 [uM] | | BioAssay | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT2B radioligand binding (ligand: [3H] Lysergic acid diethylamide) | | AID | 625217 | | BioAssay type | other | | Target | 5-hydroxytryptamine receptor 2B [gi:1168220] | | PubMed | | | Data Table |  |
|
| 11 | [SID103188158] | Active | IC50 | 0.111 | DRUGMATRIX: Alpha-1B adrenergic receptor radioligand binding (ligand: prazosin) [AID625199, Type: other] | Alpha-1B adrenergic receptor [gi:543734] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.111 [uM] | | BioAssay | DRUGMATRIX: Alpha-1B adrenergic receptor radioligand binding (ligand: prazosin) | | AID | 625199 | | BioAssay type | other | | Target | Alpha-1B adrenergic receptor [gi:543734] | | PubMed | | | Data Table |  |
|
| 12 | [SID103188158] | Active | IC50 | 0.111 | DRUGMATRIX: Alpha-1B adrenergic receptor radioligand binding (ligand: prazosin) [AID625199, Type: other] | Alpha-1B adrenergic receptor [gi:543734] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.111 [uM] | | BioAssay | DRUGMATRIX: Alpha-1B adrenergic receptor radioligand binding (ligand: prazosin) | | AID | 625199 | | BioAssay type | other | | Target | Alpha-1B adrenergic receptor [gi:543734] | | PubMed | | | Data Table |  |
|
| 13 | [SID103188158] | Active | IC50 | 0.117 | DRUGMATRIX: Alpha-1D adrenergic receptor radioligand binding (ligand: prazosin) [AID625198, Type: other] | Alpha-1D adrenergic receptor [gi:1168244] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.117 [uM] | | BioAssay | DRUGMATRIX: Alpha-1D adrenergic receptor radioligand binding (ligand: prazosin) | | AID | 625198 | | BioAssay type | other | | Target | Alpha-1D adrenergic receptor [gi:1168244] | | PubMed | | | Data Table |  |
|
| 14 | [SID103188158] | Active | IC50 | 0.192 | DRUGMATRIX: Transporter, Serotonin (5-Hydroxytryptamine) (SERT) radioligand binding (ligand: [3H] Paroxetine) [AID625222, Type: other] | Sodium-dependent serotonin transporter [gi:400630] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.192 [uM] | | BioAssay | DRUGMATRIX: Transporter, Serotonin (5-Hydroxytryptamine) (SERT) radioligand binding (ligand: [3H] Paroxetine) | | AID | 625222 | | BioAssay type | other | | Target | Sodium-dependent serotonin transporter [gi:400630] | | PubMed | | | Data Table |  |
|
| 15 | [SID103188158] | Active | IC50 | 0.192 | DRUGMATRIX: Transporter, Serotonin (5-Hydroxytryptamine) (SERT) radioligand binding (ligand: [3H] Paroxetine) [AID625222, Type: other] | Sodium-dependent serotonin transporter [gi:400630] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.192 [uM] | | BioAssay | DRUGMATRIX: Transporter, Serotonin (5-Hydroxytryptamine) (SERT) radioligand binding (ligand: [3H] Paroxetine) | | AID | 625222 | | BioAssay type | other | | Target | Sodium-dependent serotonin transporter [gi:400630] | | PubMed | | | Data Table |  |
|
| 16 | [SID103188158] | Active | IC50 | 0.192 | DRUGMATRIX: Transporter, Serotonin (5-Hydroxytryptamine) (SERT) radioligand binding (ligand: [3H] Paroxetine) [AID625222, Type: other] | Sodium-dependent serotonin transporter [gi:400630] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.192 [uM] | | BioAssay | DRUGMATRIX: Transporter, Serotonin (5-Hydroxytryptamine) (SERT) radioligand binding (ligand: [3H] Paroxetine) | | AID | 625222 | | BioAssay type | other | | Target | Sodium-dependent serotonin transporter [gi:400630] | | PubMed | | | Data Table |  |
|
| 17 | [SID103188158] | Active | IC50 | 0.265 | DRUGMATRIX: Alpha-1D adrenergic receptor radioligand binding (ligand: prazosin) [AID625200, Type: other] | Alpha-1D adrenergic receptor [gi:1168243] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.265 [uM] | | BioAssay | DRUGMATRIX: Alpha-1D adrenergic receptor radioligand binding (ligand: prazosin) | | AID | 625200 | | BioAssay type | other | | Target | Alpha-1D adrenergic receptor [gi:1168243] | | PubMed | | | Data Table |  |
|
| 18 | [SID103188158] | Active | IC50 | 0.265 | DRUGMATRIX: Alpha-1D adrenergic receptor radioligand binding (ligand: prazosin) [AID625200, Type: other] | Alpha-1D adrenergic receptor [gi:1168243] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.265 [uM] | | BioAssay | DRUGMATRIX: Alpha-1D adrenergic receptor radioligand binding (ligand: prazosin) | | AID | 625200 | | BioAssay type | other | | Target | Alpha-1D adrenergic receptor [gi:1168243] | | PubMed | | | Data Table |  |
|
| 19 | [SID103188158] | Active | IC50 | 0.265 | DRUGMATRIX: Alpha-1D adrenergic receptor radioligand binding (ligand: prazosin) [AID625200, Type: other] | Alpha-1D adrenergic receptor [gi:1168243] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.265 [uM] | | BioAssay | DRUGMATRIX: Alpha-1D adrenergic receptor radioligand binding (ligand: prazosin) | | AID | 625200 | | BioAssay type | other | | Target | Alpha-1D adrenergic receptor [gi:1168243] | | PubMed | | | Data Table |  |
|
| 20 | [SID103188158] | Active | IC50 | 0.281 | Binding affinity by its ability to displace [3H]prazosin radioligand from Alpha-1 adrenergic receptor on rat cerebral cortex [AID36712, Type: Literature] | |   View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.281 [uM] | | BioAssay | Binding affinity by its ability to displace [3H]prazosin radioligand from Alpha-1 adrenergic receptor on rat cerebral cortex | | AID | 36712 | | BioAssay type | Literature | | Target | | | PubMed | 11814815 | | Data Table |  |
|
| 21 | [SID103188158] | Active | IC50 | 0.281 | Compound was tested for the inhibition of [3H]-prazosin binding to Alpha-1 adrenergic receptor [AID36846, Type: Literature] | |   View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.281 [uM] | | BioAssay | Compound was tested for the inhibition of [3H]-prazosin binding to Alpha-1 adrenergic receptor | | AID | 36846 | | BioAssay type | Literature | | Target | | | PubMed | 9986703 | | Data Table |  |
|
| 22 | [SID103188158] | Active | IC50 | 0.311 | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT1A radioligand binding (ligand: [3H] 8-OH-DPAT) [AID625190, Type: other] | |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.311 [uM] | | BioAssay | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT1A radioligand binding (ligand: [3H] 8-OH-DPAT) | | AID | 625190 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 23 | [SID103188158] | Active | IC50 | 0.361 | DRUGMATRIX: Histamine H1, Central radioligand binding (ligand: [3H] Pyrilamine) [AID625269, Type: other] | Histamine H1 receptor [gi:547645] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.361 [uM] | | BioAssay | DRUGMATRIX: Histamine H1, Central radioligand binding (ligand: [3H] Pyrilamine) | | AID | 625269 | | BioAssay type | other | | Target | Histamine H1 receptor [gi:547645] | | PubMed | | | Data Table |  |
|
| 24 | [SID103188158] | Active | IC50 | 0.361 | DRUGMATRIX: Histamine H1, Central radioligand binding (ligand: [3H] Pyrilamine) [AID625269, Type: other] | Histamine H1 receptor [gi:547645] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.361 [uM] | | BioAssay | DRUGMATRIX: Histamine H1, Central radioligand binding (ligand: [3H] Pyrilamine) | | AID | 625269 | | BioAssay type | other | | Target | Histamine H1 receptor [gi:547645] | | PubMed | | | Data Table |  |
|
| 25 | [SID103188158] | Active | IC50 | 0.389 | DRUGMATRIX: Alpha-2B adrenergic receptor radioligand binding (ligand: Rauwolscine) [AID625202, Type: other] | Alpha-2B adrenergic receptor [gi:27151763] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.389 [uM] | | BioAssay | DRUGMATRIX: Alpha-2B adrenergic receptor radioligand binding (ligand: Rauwolscine) | | AID | 625202 | | BioAssay type | other | | Target | Alpha-2B adrenergic receptor [gi:27151763] | | PubMed | | | Data Table |  |
|
| 26 | [SID103188158] | Active | IC50 | 0.389 | DRUGMATRIX: Alpha-2B adrenergic receptor radioligand binding (ligand: Rauwolscine) [AID625202, Type: other] | Alpha-2B adrenergic receptor [gi:27151763] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.389 [uM] | | BioAssay | DRUGMATRIX: Alpha-2B adrenergic receptor radioligand binding (ligand: Rauwolscine) | | AID | 625202 | | BioAssay type | other | | Target | Alpha-2B adrenergic receptor [gi:27151763] | | PubMed | | | Data Table |  |
|
| 27 | [SID103188158] | Active | IC50 | 0.909 | DRUGMATRIX: Alpha-2A adrenergic receptor radioligand binding (ligand: MK-912) [AID625201, Type: other] | Alpha-2A adrenergic receptor [gi:1351829] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.909 [uM] | | BioAssay | DRUGMATRIX: Alpha-2A adrenergic receptor radioligand binding (ligand: MK-912) | | AID | 625201 | | BioAssay type | other | | Target | Alpha-2A adrenergic receptor [gi:1351829] | | PubMed | | | Data Table |  |
|
| 28 | [SID103188158] | Active | IC50 | 0.909 | DRUGMATRIX: Alpha-2A adrenergic receptor radioligand binding (ligand: MK-912) [AID625201, Type: other] | Alpha-2A adrenergic receptor [gi:1351829] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 0.909 [uM] | | BioAssay | DRUGMATRIX: Alpha-2A adrenergic receptor radioligand binding (ligand: MK-912) | | AID | 625201 | | BioAssay type | other | | Target | Alpha-2A adrenergic receptor [gi:1351829] | | PubMed | | | Data Table |  |
|
| 29 | [SID103188158] | Active | IC50 | 1.342 | DRUGMATRIX: Sigma2 radioligand binding (ligand: [3H] Ifenprodil) [AID625224, Type: other] | |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 1.342 [uM] | | BioAssay | DRUGMATRIX: Sigma2 radioligand binding (ligand: [3H] Ifenprodil) | | AID | 625224 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 30 | [SID103188158] | Active | IC50 | 1.356 | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT1B radioligand binding (ligand: [125I] Cyanopindolol) [AID625191, Type: other] | 5-hydroxytryptamine receptor 1B [gi:112815] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 1.356 [uM] | | BioAssay | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT1B radioligand binding (ligand: [125I] Cyanopindolol) | | AID | 625191 | | BioAssay type | other | | Target | 5-hydroxytryptamine receptor 1B [gi:112815] | | PubMed | | | Data Table |  |
|
| 31 | [SID103188158] | Active | IC50 | 1.356 | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT1B radioligand binding (ligand: [125I] Cyanopindolol) [AID625191, Type: other] | 5-hydroxytryptamine receptor 1B [gi:112815] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 1.356 [uM] | | BioAssay | DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT1B radioligand binding (ligand: [125I] Cyanopindolol) | | AID | 625191 | | BioAssay type | other | | Target | 5-hydroxytryptamine receptor 1B [gi:112815] | | PubMed | | | Data Table |  |
|
| 32 | [SID103188158] | Active | IC50 | 1.942 | DRUGMATRIX: Adrenergic Alpha-2C radioligand binding (ligand: [3H] MK-912) [AID625203, Type: other] | Alpha-2C adrenergic receptor [gi:20141211] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 1.942 [uM] | | BioAssay | DRUGMATRIX: Adrenergic Alpha-2C radioligand binding (ligand: [3H] MK-912) | | AID | 625203 | | BioAssay type | other | | Target | Alpha-2C adrenergic receptor [gi:20141211] | | PubMed | | | Data Table |  |
|
| 33 | [SID103188158] | Active | IC50 | 1.942 | DRUGMATRIX: Adrenergic Alpha-2C radioligand binding (ligand: [3H] MK-912) [AID625203, Type: other] | Alpha-2C adrenergic receptor [gi:20141211] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 1.942 [uM] | | BioAssay | DRUGMATRIX: Adrenergic Alpha-2C radioligand binding (ligand: [3H] MK-912) | | AID | 625203 | | BioAssay type | other | | Target | Alpha-2C adrenergic receptor [gi:20141211] | | PubMed | | | Data Table |  |
|
| 34 | [SID103188158] | Active | IC50 | 2.203 | DRUGMATRIX: Sigma1 radioligand binding (ligand: [3H] Haloperidol) [AID625223, Type: other] | Sigma non-opioid intracellular receptor 1 [gi:74752153] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 2.203 [uM] | | BioAssay | DRUGMATRIX: Sigma1 radioligand binding (ligand: [3H] Haloperidol) | | AID | 625223 | | BioAssay type | other | | Target | Sigma non-opioid intracellular receptor 1 [gi:74752153] | | PubMed | | | Data Table |  |
|
| 35 | [SID103188158] | Active | IC50 | 2.203 | DRUGMATRIX: Sigma1 radioligand binding (ligand: [3H] Haloperidol) [AID625223, Type: other] | Sigma non-opioid intracellular receptor 1 [gi:74752153] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 2.203 [uM] | | BioAssay | DRUGMATRIX: Sigma1 radioligand binding (ligand: [3H] Haloperidol) | | AID | 625223 | | BioAssay type | other | | Target | Sigma non-opioid intracellular receptor 1 [gi:74752153] | | PubMed | | | Data Table |  |
|
| 36 | [SID103188158] | Active | IC50 | 2.891 | DRUGMATRIX: Imidazoline I2, Central radioligand binding (ligand: [3H] Idazoxan) [AID625272, Type: other] | |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 2.891 [uM] | | BioAssay | DRUGMATRIX: Imidazoline I2, Central radioligand binding (ligand: [3H] Idazoxan) | | AID | 625272 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 37 | [SID103188158] | Active | IC50 | 3.743 | DRUGMATRIX: Dopamine D3 radioligand binding (ligand: [3H] Spiperone) [AID625254, Type: other] | D(3) dopamine receptor [gi:1169206] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 3.743 [uM] | | BioAssay | DRUGMATRIX: Dopamine D3 radioligand binding (ligand: [3H] Spiperone) | | AID | 625254 | | BioAssay type | other | | Target | D(3) dopamine receptor [gi:1169206] | | PubMed | | | Data Table |  |
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| 38 | [SID103188158] | Active | IC50 | 3.743 | DRUGMATRIX: Dopamine D3 radioligand binding (ligand: [3H] Spiperone) [AID625254, Type: other] | D(3) dopamine receptor [gi:1169206] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 3.743 [uM] | | BioAssay | DRUGMATRIX: Dopamine D3 radioligand binding (ligand: [3H] Spiperone) | | AID | 625254 | | BioAssay type | other | | Target | D(3) dopamine receptor [gi:1169206] | | PubMed | | | Data Table |  |
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| 39 | [SID103188158] | Active | IC50 | 3.743 | DRUGMATRIX: Dopamine D3 radioligand binding (ligand: [3H] Spiperone) [AID625254, Type: other] | D(3) dopamine receptor [gi:1169206] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 3.743 [uM] | | BioAssay | DRUGMATRIX: Dopamine D3 radioligand binding (ligand: [3H] Spiperone) | | AID | 625254 | | BioAssay type | other | | Target | D(3) dopamine receptor [gi:1169206] | | PubMed | | | Data Table |  |
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| 40 | [SID103188158] | Active | IC50 | 3.743 | DRUGMATRIX: Dopamine D3 radioligand binding (ligand: [3H] Spiperone) [AID625254, Type: other] | D(3) dopamine receptor [gi:1169206] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 103188158 | | CID | 5533 | | Outcome | Active | | IC50 | 3.743 [uM] | | BioAssay | DRUGMATRIX: Dopamine D3 radioligand binding (ligand: [3H] Spiperone) | | AID | 625254 | | BioAssay type | other | | Target | D(3) dopamine receptor [gi:1169206] | | PubMed | | | Data Table |  |
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| 41 | [SID11111901] | Active | Potency | 11.2202 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 11111901 | | CID | 5533 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
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| 42 | [SID11111901] | Active | Potency | 11.2202 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 11111901 | | CID | 5533 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
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| 43 | [SID90341328] | Active | Potency | 11.2202 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists [AID488983, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 90341328 | | CID | 5533 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists | | AID | 488983 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
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| 44 | [SID90341328] | Active | Potency | 11.2202 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists [AID488983, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 90341328 | | CID | 5533 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists | | AID | 488983 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
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| 45 | [SID90341328] | Active | Potency | 11.2202 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists [AID488983, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 90341328 | | CID | 5533 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists | | AID | 488983 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
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| 46 | [SID90341328] | Active | Potency | 11.2202 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists [AID488983, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 90341328 | | CID | 5533 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists | | AID | 488983 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
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| 47 | [SID11111901] | Active | Potency | 15.8489 | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 [AID893, Type: confirmatory] | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 11111901 | | CID | 5533 | | Outcome | Active | | Potency | 15.8489 [uM] | | BioAssay | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 | | AID | 893 | | BioAssay type | confirmatory | | Target | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] | | PubMed | | | Data Table |  |
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| 48 | [SID11111900] | Active | Potency | 31.6228 | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 [AID893, Type: confirmatory] | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 11111900 | | CID | 5533 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 | | AID | 893 | | BioAssay type | confirmatory | | Target | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] | | PubMed | | | Data Table |  |
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| 49 | [SID11111900] | Active | | | qHTS Assay for Spectroscopic Profiling in 4-MU Spectral Region [AID589, Type: other] | |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 11111900 | | CID | 5533 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in 4-MU Spectral Region | | AID | 589 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 50 | [SID11111900] | Active | | | qHTS Assay for Spectroscopic Profiling in A350 Spectral Region [AID590, Type: other] | |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 11111900 | | CID | 5533 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in A350 Spectral Region | | AID | 590 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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