| 1 | [SID103355081] | Active | IC50 | 0.026 | Inhibitory activity against human PARP1 expressed in PC12 cells [AID259509, Type: Literature] | Poly [ADP-ribose] polymerase 1 [gi:130781] |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Active | | IC50 | 0.026 [uM] | | BioAssay | Inhibitory activity against human PARP1 expressed in PC12 cells | | AID | 259509 | | BioAssay type | Literature | | Target | Poly [ADP-ribose] polymerase 1 [gi:130781] | | PubMed | 16290935 | | Data Table |  |
|
| 2 | [SID103355081] | Active | IC50 | 0.18 | The compound was tested for poly(ADP-ribose)-polymerase (PARP) inhibition [AID154621, Type: Literature] | |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Active | | IC50 | 0.18 [uM] | | BioAssay | The compound was tested for poly(ADP-ribose)-polymerase (PARP) inhibition | | AID | 154621 | | BioAssay type | Literature | | Target | | | PubMed | 11689065 | | Data Table |  |
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| 3 | [SID103355081] | Active | IC50 | 0.18 | In vitro cytotoxicity against human lung carcinoma A549 cells [AID247676, Type: Literature] | |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Active | | IC50 | 0.18 [uM] | | BioAssay | In vitro cytotoxicity against human lung carcinoma A549 cells | | AID | 247676 | | BioAssay type | Literature | | Target | | | PubMed | 15481984 | | Data Table |  |
|
| 4 | [SID11110714] | Active | Potency | 0.7943 | qHTS Assay for Inhibitors of RGS12 GoLoco Motif Activity (Green Fluorophore) [AID879, Type: confirmatory] | RGS12 [Homo sapiens] [gi:3290016] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 11110714 | | CID | 1720 | | Outcome | Active | | Potency | 0.7943 [uM] | | BioAssay | qHTS Assay for Inhibitors of RGS12 GoLoco Motif Activity (Green Fluorophore) | | AID | 879 | | BioAssay type | confirmatory | | Target | RGS12 [Homo sapiens] [gi:3290016] | | PubMed | | | Data Table |  |
|
| 5 | [SID50105795] | Active | Potency | 5.0119 | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity [AID588834, Type: Literature] | KCNH2 gene product [Homo sapiens] [gi:325651834] |   View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 50105795 | | CID | 1720 | | Outcome | Active | | Potency | 5.0119 [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity | | AID | 588834 | | BioAssay type | Literature | | Target | KCNH2 gene product [Homo sapiens] [gi:325651834] | | PubMed | 19583963 | | Data Table |  |
|
| 6 | [SID50105795] | Active | Potency | 5.0119 | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity [AID588834, Type: Literature] | KCNH2 gene product [Homo sapiens] [gi:325651834] |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 50105795 | | CID | 1720 | | Outcome | Active | | Potency | 5.0119 [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity | | AID | 588834 | | BioAssay type | Literature | | Target | KCNH2 gene product [Homo sapiens] [gi:325651834] | | PubMed | 19583963 | | Data Table |  |
|
| 7 | [SID50105795] | Active | Potency | 5.0119 | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity [AID588834, Type: Literature] | KCNH2 gene product [Homo sapiens] [gi:325651834] |   View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 50105795 | | CID | 1720 | | Outcome | Active | | Potency | 5.0119 [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity | | AID | 588834 | | BioAssay type | Literature | | Target | KCNH2 gene product [Homo sapiens] [gi:325651834] | | PubMed | 19583963 | | Data Table |  |
|
| 8 | [SID50105795] | Active | Potency | 5.0119 | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity [AID588834, Type: Literature] | KCNH2 gene product [Homo sapiens] [gi:325651834] |   View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 50105795 | | CID | 1720 | | Outcome | Active | | Potency | 5.0119 [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity | | AID | 588834 | | BioAssay type | Literature | | Target | KCNH2 gene product [Homo sapiens] [gi:325651834] | | PubMed | 19583963 | | Data Table |  |
|
| 9 | [SID50105795] | Active | Potency | 5.0119 | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity [AID588834, Type: Literature] | KCNH2 gene product [Homo sapiens] [gi:325651834] |   View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 50105795 | | CID | 1720 | | Outcome | Active | | Potency | 5.0119 [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity | | AID | 588834 | | BioAssay type | Literature | | Target | KCNH2 gene product [Homo sapiens] [gi:325651834] | | PubMed | 19583963 | | Data Table |  |
|
| 10 | [SID103355081] | Active | IC50 | 7.94328 | Antiplasmodial activity against Plasmodium falciparum 3D7 after 72 hrs by SYBR green assay [AID524790, Type: Literature] | |   View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Active | | IC50 | 7.94328 [uM] | | BioAssay | Antiplasmodial activity against Plasmodium falciparum 3D7 after 72 hrs by SYBR green assay | | AID | 524790 | | BioAssay type | Literature | | Target | | | PubMed | 19734910 | | Data Table |  |
|
| 11 | [SID90340784] | Active | Potency | 11.2202 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists [AID488981, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 90340784 | | CID | 1720 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists | | AID | 488981 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 12 | [SID90340784] | Active | Potency | 11.2202 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists [AID488981, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 90340784 | | CID | 1720 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists | | AID | 488981 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 13 | [SID90340784] | Active | Potency | 11.2202 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists [AID488981, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 90340784 | | CID | 1720 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists | | AID | 488981 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 14 | [SID90340784] | Active | Potency | 11.2202 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists [AID488981, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 90340784 | | CID | 1720 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists | | AID | 488981 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 15 | [SID11110714] | Active | Potency | 12.5893 | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Green Fluorophore) [AID875, Type: confirmatory] | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 11110714 | | CID | 1720 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Green Fluorophore) | | AID | 875 | | BioAssay type | confirmatory | | Target | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] | | PubMed | | | Data Table |  |
|
| 16 | [SID26753511] | Active | Potency | 17.7828 | Quantitative High-Throughput Screen for Regulators of Epigenetic Control [AID1865, Type: confirmatory] | |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 26753511 | | CID | 1720 | | Outcome | Active | | Potency | 17.7828 [uM] | | BioAssay | Quantitative High-Throughput Screen for Regulators of Epigenetic Control | | AID | 1865 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 17 | [SID50105795] | Active | Potency | 25.1189 | 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. | 17 | | Structure |
| | Substance | | | SID | 50105795 | | CID | 1720 | | Outcome | Active | | Potency | 25.1189 [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 |  |
|
| 18 | [SID90340784] | Active | Potency | 25.1189 | Inhibitors of USP1/UAF1: Pilot qHTS [AID504865, Type: confirmatory] | USP1 protein [Homo sapiens] [gi:118600387] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 90340784 | | CID | 1720 | | Outcome | Active | | Potency | 25.1189 [uM] | | BioAssay | Inhibitors of USP1/UAF1: Pilot qHTS | | AID | 504865 | | BioAssay type | confirmatory | | Target | USP1 protein [Homo sapiens] [gi:118600387] | | PubMed | | | Data Table |  |
|
| 19 | [SID11110714] | Active | Potency | 31.6228 | qHTS Assay for Modulators of Hemoglobin Beta Chain Splicing [AID925, Type: confirmatory] | hemoglobin subunit beta [Homo sapiens] [gi:4504349] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 11110714 | | CID | 1720 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | qHTS Assay for Modulators of Hemoglobin Beta Chain Splicing | | AID | 925 | | BioAssay type | confirmatory | | Target | hemoglobin subunit beta [Homo sapiens] [gi:4504349] | | PubMed | | | Data Table |  |
|
| 20 | [SID26753511] | Active | Potency | 50.1187 | 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. | 20 | | Structure |
| | Substance | | | SID | 26753511 | | CID | 1720 | | Outcome | Active | | Potency | 50.1187 [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 |  |
|
| 21 | [SID85788267] | Active | | | Luminescence Homogenous Primary HTS to Identify Inhibitors of STK33 Activity [AID2322, Type: screening] | |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 85788267 | | CID | 1720 | | Outcome | Active | | BioAssay | Luminescence Homogenous Primary HTS to Identify Inhibitors of STK33 Activity | | AID | 2322 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 22 | [SID46394321] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, The Catalytic Fragment Of Poly(Adp-Ribose) Polymerase Complexed With 4-Amino-1,8-Naphthalim [gi:157835644] |   View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 46394321 | | CID | 1720 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, The Catalytic Fragment Of Poly(Adp-Ribose) Polymerase Complexed With 4-Amino-1,8-Naphthalim [gi:157835644] | | PubMed | 9521710 | | Data Table |  |
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| 23 | [SID11110714] | Active | | | qHTS Assay for Spectroscopic Profiling in A488 Spectral Region [AID591, Type: other] | |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 11110714 | | CID | 1720 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in A488 Spectral Region | | AID | 591 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 24 | [SID11110714] | Active | | | qHTS Assay for Spectroscopic Profiling in Fluorescein Spectral Region [AID593, Type: other] | |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 11110714 | | CID | 1720 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in Fluorescein Spectral Region | | AID | 593 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 25 | [SID103855809] | Active | | | Wombat Data for BeliefDocking [AID493017, Type: Literature] | [geneid:142] |   View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 103855809 | | CID | 1720 | | Outcome | Active | | BioAssay | Wombat Data for BeliefDocking | | AID | 493017 | | BioAssay type | Literature | | Target | [geneid:142] | | PubMed | 11689065 | | Data Table |  |
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| 26 | [SID11110714] | Active | | | p450-cyp1a2 [AID410, Type: confirmatory] | cytochrome P450, family 1, subfamily A, polypeptide 2 [Homo sapiens] [gi:73915100] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 11110714 | | CID | 1720 | | Outcome | Active | | BioAssay | p450-cyp1a2 | | AID | 410 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 1, subfamily A, polypeptide 2 [Homo sapiens] [gi:73915100] | | PubMed | | | Data Table |  |
|
| 27 | [SID11110714] | Active | | | p450-cyp1a2 [AID410, Type: confirmatory] | cytochrome P450, family 1, subfamily A, polypeptide 2 [Homo sapiens] [gi:73915100] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 11110714 | | CID | 1720 | | Outcome | Active | | BioAssay | p450-cyp1a2 | | AID | 410 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 1, subfamily A, polypeptide 2 [Homo sapiens] [gi:73915100] | | PubMed | | | Data Table |  |
|
| 28 | [SID11110714] | Active | | | p450-cyp1a2 [AID410, Type: confirmatory] | cytochrome P450, family 1, subfamily A, polypeptide 2 [Homo sapiens] [gi:73915100] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 11110714 | | CID | 1720 | | Outcome | Active | | BioAssay | p450-cyp1a2 | | AID | 410 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 1, subfamily A, polypeptide 2 [Homo sapiens] [gi:73915100] | | PubMed | | | Data Table |  |
|
| 29 | [SID11110714] | Active | | | Cytochrome panel assay with activity outcomes [AID1851_4, Type: other] | cytochrome P450, family 1, subfamily A, polypeptide 2 [Homo sapiens] [gi:73915100] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 11110714 | | CID | 1720 | | Outcome | Active | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 1, subfamily A, polypeptide 2 [Homo sapiens] [gi:73915100] | | PubMed | | | Data Table |  |
|
| 30 | [SID11110714] | Active | | | Cytochrome panel assay with activity outcomes [AID1851_4, Type: other] | cytochrome P450, family 1, subfamily A, polypeptide 2 [Homo sapiens] [gi:73915100] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 11110714 | | CID | 1720 | | Outcome | Active | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 1, subfamily A, polypeptide 2 [Homo sapiens] [gi:73915100] | | PubMed | | | Data Table |  |
|
| 31 | [SID50105795] | Active | | | qHTS Assay for Inhibitors of RGS12 GoLoco Motif Activity (Red Fluorophore) [AID880, Type: confirmatory] | RGS12 [Homo sapiens] [gi:3290016] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 50105795 | | CID | 1720 | | Outcome | Active | | BioAssay | qHTS Assay for Inhibitors of RGS12 GoLoco Motif Activity (Red Fluorophore) | | AID | 880 | | BioAssay type | confirmatory | | Target | RGS12 [Homo sapiens] [gi:3290016] | | PubMed | | | Data Table |  |
|
| 32 | [SID26753511] | Active | | | qHTS Assay for Inhibitors of RGS12 GoLoco Motif Activity (Red Fluorophore) [AID880, Type: confirmatory] | RGS12 [Homo sapiens] [gi:3290016] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 26753511 | | CID | 1720 | | Outcome | Active | | BioAssay | qHTS Assay for Inhibitors of RGS12 GoLoco Motif Activity (Red Fluorophore) | | AID | 880 | | BioAssay type | confirmatory | | Target | RGS12 [Homo sapiens] [gi:3290016] | | PubMed | | | Data Table |  |
|
| 33 | [SID50105795] | Active | | | qHTS for Small Molecule Agonists and Allosteric Enhancers of Human TRH Receptor: Validation Screen for Agonists [AID493127, Type: screening] | thyrotropin-releasing hormone receptor [Homo sapiens] [gi:4507681] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 50105795 | | CID | 1720 | | Outcome | Active | | BioAssay | qHTS for Small Molecule Agonists and Allosteric Enhancers of Human TRH Receptor: Validation Screen for Agonists | | AID | 493127 | | BioAssay type | screening | | Target | thyrotropin-releasing hormone receptor [Homo sapiens] [gi:4507681] | | PubMed | | | Data Table |  |
|
| 34 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Tachykinin NK2 radioligand binding (ligand: [3H] SR-48968) [AID625227, Type: other] | Substance-K receptor [gi:229462950] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Tachykinin NK2 radioligand binding (ligand: [3H] SR-48968) | | AID | 625227 | | BioAssay type | other | | Target | Substance-K receptor [gi:229462950] | | PubMed | | | Data Table |  |
|
| 35 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Tachykinin NK1 radioligand binding (ligand: [3H] Substance P) [AID625226, Type: other] | Substance-P receptor [gi:128359] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Tachykinin NK1 radioligand binding (ligand: [3H] Substance P) | | AID | 625226 | | BioAssay type | other | | Target | Substance-P receptor [gi:128359] | | PubMed | | | Data Table |  |
|
| 36 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Tachykinin NK1 radioligand binding (ligand: [3H] Substance P) [AID625226, Type: other] | Substance-P receptor [gi:128359] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Tachykinin NK1 radioligand binding (ligand: [3H] Substance P) | | AID | 625226 | | BioAssay type | other | | Target | Substance-P receptor [gi:128359] | | PubMed | | | Data Table |  |
|
| 37 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Thromboxane Synthetase enzyme inhibition (substrate: PGH2) [AID625229, Type: other] | Thromboxane-A synthase [gi:254763392] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Thromboxane Synthetase enzyme inhibition (substrate: PGH2) | | AID | 625229 | | BioAssay type | other | | Target | Thromboxane-A synthase [gi:254763392] | | PubMed | | | Data Table |  |
|
| 38 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Cyclooxygenase COX-1 enzyme inhibition (substrate: Arachidonic acid) [AID625243, Type: other] | Prostaglandin G/H synthase 1 [gi:317373262] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Cyclooxygenase COX-1 enzyme inhibition (substrate: Arachidonic acid) | | AID | 625243 | | BioAssay type | other | | Target | Prostaglandin G/H synthase 1 [gi:317373262] | | PubMed | | | Data Table |  |
|
| 39 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Cyclooxygenase COX-2 enzyme inhibition (substrate: Arachidonic acid) [AID625244, Type: other] | Prostaglandin G/H synthase 2 [gi:3915797] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Cyclooxygenase COX-2 enzyme inhibition (substrate: Arachidonic acid) | | AID | 625244 | | BioAssay type | other | | Target | Prostaglandin G/H synthase 2 [gi:3915797] | | PubMed | | | Data Table |  |
|
| 40 | [SID103355081] | Unspecified | | | DRUGMATRIX: Protein Tyrosine Phosphatase, PTPRC (CD45) enzyme inhibition (substrate: DiFMUP) [AID625188, Type: other] | Receptor-type tyrosine-protein phosphatase C [gi:33112650] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | BioAssay | DRUGMATRIX: Protein Tyrosine Phosphatase, PTPRC (CD45) enzyme inhibition (substrate: DiFMUP) | | AID | 625188 | | BioAssay type | other | | Target | Receptor-type tyrosine-protein phosphatase C [gi:33112650] | | PubMed | | | Data Table |  |
|
| 41 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Norepinephrine Transporter radioligand binding (ligand: [125I] RTI-55) [AID625207, Type: other] | Sodium-dependent noradrenaline transporter [gi:128616] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Norepinephrine Transporter radioligand binding (ligand: [125I] RTI-55) | | AID | 625207 | | BioAssay type | other | | Target | Sodium-dependent noradrenaline transporter [gi:128616] | | PubMed | | | Data Table |  |
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| 42 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Norepinephrine Transporter radioligand binding (ligand: [125I] RTI-55) [AID625207, Type: other] | Sodium-dependent noradrenaline transporter [gi:128616] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Norepinephrine Transporter radioligand binding (ligand: [125I] RTI-55) | | AID | 625207 | | BioAssay type | other | | Target | Sodium-dependent noradrenaline transporter [gi:128616] | | PubMed | | | Data Table |  |
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| 43 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Dopamine Transporter radioligand binding (ligand: [125I] RTI-55) [AID625256, Type: other] | Sodium-dependent dopamine transporter [gi:266667] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Dopamine Transporter radioligand binding (ligand: [125I] RTI-55) | | AID | 625256 | | BioAssay type | other | | Target | Sodium-dependent dopamine transporter [gi:266667] | | PubMed | | | Data Table |  |
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| 44 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Dopamine Transporter radioligand binding (ligand: [125I] RTI-55) [AID625256, Type: other] | Sodium-dependent dopamine transporter [gi:266667] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Dopamine Transporter radioligand binding (ligand: [125I] RTI-55) | | AID | 625256 | | BioAssay type | other | | Target | Sodium-dependent dopamine transporter [gi:266667] | | PubMed | | | Data Table |  |
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| 45 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Dopamine Transporter radioligand binding (ligand: [125I] RTI-55) [AID625256, Type: other] | Sodium-dependent dopamine transporter [gi:266667] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Dopamine Transporter radioligand binding (ligand: [125I] RTI-55) | | AID | 625256 | | BioAssay type | other | | Target | Sodium-dependent dopamine transporter [gi:266667] | | PubMed | | | Data Table |  |
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| 46 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Dopamine Transporter radioligand binding (ligand: [125I] RTI-55) [AID625256, Type: other] | Sodium-dependent dopamine transporter [gi:266667] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Dopamine Transporter radioligand binding (ligand: [125I] RTI-55) | | AID | 625256 | | BioAssay type | other | | Target | Sodium-dependent dopamine transporter [gi:266667] | | PubMed | | | Data Table |  |
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| 47 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Transporter, Serotonin (5-Hydroxytryptamine) (SERT) radioligand binding (ligand: [3H] Paroxetine) [AID625222, Type: other] | Sodium-dependent serotonin transporter [gi:400630] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [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 |  |
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| 48 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Transporter, Serotonin (5-Hydroxytryptamine) (SERT) radioligand binding (ligand: [3H] Paroxetine) [AID625222, Type: other] | Sodium-dependent serotonin transporter [gi:400630] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [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 |  |
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| 49 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Transporter, Serotonin (5-Hydroxytryptamine) (SERT) radioligand binding (ligand: [3H] Paroxetine) [AID625222, Type: other] | Sodium-dependent serotonin transporter [gi:400630] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [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 |  |
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| 50 | [SID103355081] | Unspecified | IC50 | | DRUGMATRIX: Melanocortin MC3 radioligand binding (ligand: [125I] NDP-alpha-MSH) [AID625147, Type: other] | Melanocortin receptor 3 [gi:395398606] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 103355081 | | CID | 1720 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Melanocortin MC3 radioligand binding (ligand: [125I] NDP-alpha-MSH) | | AID | 625147 | | BioAssay type | other | | Target | Melanocortin receptor 3 [gi:395398606] | | PubMed | | | Data Table |  |
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