| 1 | [SID103372397] | Active | IC50 | 0.001 | Inhibition of human AchE [AID314091, Type: Literature] | Acetylcholinesterase [gi:113037] |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Active | | IC50 | 0.001 [uM] | | BioAssay | Inhibition of human AchE | | AID | 314091 | | BioAssay type | Literature | | Target | Acetylcholinesterase [gi:113037] | | PubMed | 18181565 | | Data Table |  |
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| 2 | [SID103372397] | Active | IC50 | 1.95 | Antioxidant activity assessed as hypochlorous acid scavenging activity by fluorescent rhodamine formation assay [AID453279, Type: Literature] | |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Active | | IC50 | 1.95 [uM] | | BioAssay | Antioxidant activity assessed as hypochlorous acid scavenging activity by fluorescent rhodamine formation assay | | AID | 453279 | | BioAssay type | Literature | | Target | | | PubMed | 19781949 | | Data Table |  |
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| 3 | [SID103372397] | Active | IC50 | 2.4 | Hypochlorous acid scavenging activity assessed as inhibition of DHR oxidation [AID289322, Type: Literature] | |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Active | | IC50 | 2.4 [uM] | | BioAssay | Hypochlorous acid scavenging activity assessed as inhibition of DHR oxidation | | AID | 289322 | | BioAssay type | Literature | | Target | | | PubMed | 17624791 | | Data Table |  |
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| 4 | [SID103372397] | Active | IC50 | 11 | Antioxidant activity assessed as hydroxyl radical scavenging activity [AID347225, Type: Literature] | |   View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Active | | IC50 | 11 [uM] | | BioAssay | Antioxidant activity assessed as hydroxyl radical scavenging activity | | AID | 347225 | | BioAssay type | Literature | | Target | | | PubMed | 19097798 | | Data Table |  |
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| 5 | [SID103372397] | Active | IC50 | 19.6 | Neuroprotective effect was measured by its ability to protect mouse hippocampal neuronal HT-22 cell lines from oxidative stress caused by glutamate [AID84280, Type: Literature] | |   View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Active | | IC50 | 19.6 [uM] | | BioAssay | Neuroprotective effect was measured by its ability to protect mouse hippocampal neuronal HT-22 cell lines from oxidative stress caused by glutamate | | AID | 84280 | | BioAssay type | Literature | | Target | | | PubMed | 12031315 | | Data Table |  |
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| 6 | [SID103372397] | Active | | | Radical reducing potency by ABTS cation radical reduction assay per 30 mins at 1 umol/mL [AID264481, Type: Literature] | |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Active | | BioAssay | Radical reducing potency by ABTS cation radical reduction assay per 30 mins at 1 umol/mL | | AID | 264481 | | BioAssay type | Literature | | Target | | | PubMed | 16640342 | | Data Table |  |
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| 7 | [SID103372397] | Unspecified | Kd | 10 | Blocking activity was assessed by antagonism of (-)-phenylephrine induced contraction of rat spleen (alpha1B adrenoceptor) [AID239871, Type: Literature] | |   View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | Kd | 10 [uM] | | BioAssay | Blocking activity was assessed by antagonism of (-)-phenylephrine induced contraction of rat spleen (alpha1B adrenoceptor) | | AID | 239871 | | BioAssay type | Literature | | Target | | | PubMed | 15633998 | | Data Table |  |
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| 8 | [SID103372397] | Unspecified | Kd | 10 | Blocking activity was assessed by antagonism of (-)-noradrenaline induced contraction of rat thoracic aorta (Alpha-1D adrenoceptor) [AID239872, Type: Literature] | |   View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | Kd | 10 [uM] | | BioAssay | Blocking activity was assessed by antagonism of (-)-noradrenaline induced contraction of rat thoracic aorta (Alpha-1D adrenoceptor) | | AID | 239872 | | BioAssay type | Literature | | Target | | | PubMed | 15633998 | | Data Table |  |
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| 9 | [SID103372397] | Unspecified | Kd | 10 | Blocking activity was assessed by antagonism of (-)-noradrenaline induced contraction of rat prostatic vas deferens (alpha1A adrenoceptor) [AID239873, Type: Literature] | |   View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | Kd | 10 [uM] | | BioAssay | Blocking activity was assessed by antagonism of (-)-noradrenaline induced contraction of rat prostatic vas deferens (alpha1A adrenoceptor) | | AID | 239873 | | BioAssay type | Literature | | Target | | | PubMed | 15633998 | | Data Table |  |
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| 10 | [SID103372397] | Unspecified | IC50 | 54.86 | Antioxidant activity against formation of ROS was determined in t-BuOOH treated LNCaP cells after 24 hr of incubation with compounds (1-100 uM) [AID248861, Type: Literature] | |   View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | 54.86 [uM] | | BioAssay | Antioxidant activity against formation of ROS was determined in t-BuOOH treated LNCaP cells after 24 hr of incubation with compounds (1-100 uM) | | AID | 248861 | | BioAssay type | Literature | | Target | | | PubMed | 15633998 | | Data Table |  |
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| 11 | [SID103372397] | Unspecified | EC50 | 121.6 | Ability for prevention of GSH depletion was measured in mouse [AID127631, Type: Literature] | |   View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | EC50 | 121.6 [uM] | | BioAssay | Ability for prevention of GSH depletion was measured in mouse | | AID | 127631 | | BioAssay type | Literature | | Target | | | PubMed | 12031315 | | Data Table |  |
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| 12 | [SID103372397] | Unspecified | EC50 | 250 | Induction of apoptosis in human HT-29 cells [AID481542, Type: Literature] | |   View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | EC50 | 250 [uM] | | BioAssay | Induction of apoptosis in human HT-29 cells | | AID | 481542 | | BioAssay type | Literature | | Target | | | PubMed | 20403695 | | Data Table |  |
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| 13 | [SID103372397] | Unspecified | IC50 | 400 | Evaluated for the interaction with 0.2 mM of the stable free radical DPPH. [AID197086, Type: Literature] | |   View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | 400 [uM] | | BioAssay | Evaluated for the interaction with 0.2 mM of the stable free radical DPPH. | | AID | 197086 | | BioAssay type | Literature | | Target | | | PubMed | 11708933 | | Data Table |  |
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| 14 | [SID103372397] | Unspecified | IC50 | 1000 | Inhibition of in vitro peroxidation (LP) of rat Hepatic microsomal membrane lipid [AID197084, Type: Literature] | |   View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | 1000 [uM] | | BioAssay | Inhibition of in vitro peroxidation (LP) of rat Hepatic microsomal membrane lipid | | AID | 197084 | | BioAssay type | Literature | | Target | | | PubMed | 11708933 | | Data Table |  |
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| 15 | [SID103372397] | Unspecified | IC50 | 1000 | Inhibition of human serum recombinant AChE after 20 mins using acetylthiocholine iodide as a substrate by Ellman's assay [AID625546, Type: Literature] | Acetylcholinesterase [gi:113037] |   View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | 1000 [uM] | | BioAssay | Inhibition of human serum recombinant AChE after 20 mins using acetylthiocholine iodide as a substrate by Ellman's assay | | AID | 625546 | | BioAssay type | Literature | | Target | Acetylcholinesterase [gi:113037] | | PubMed | 21924801 | | Data Table |  |
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| 16 | [SID103372397] | Unspecified | IC50 | 1000 | Inhibitory concentration against human recombinant acetylcholinesterase [AID241200, Type: Literature] | Acetylcholinesterase [gi:113037] |   View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | 1000 [uM] | | BioAssay | Inhibitory concentration against human recombinant acetylcholinesterase | | AID | 241200 | | BioAssay type | Literature | | Target | Acetylcholinesterase [gi:113037] | | PubMed | 15658850 | | Data Table |  |
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| 17 | [SID103372397] | Unspecified | IC50 | 1000 | Inhibitory concentration against human recombinant butyrylcholinesterase [AID241230, Type: Literature] | Cholinesterase [gi:116353] |   View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | 1000 [uM] | | BioAssay | Inhibitory concentration against human recombinant butyrylcholinesterase | | AID | 241230 | | BioAssay type | Literature | | Target | Cholinesterase [gi:116353] | | PubMed | 15658850 | | Data Table |  |
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| 18 | [SID103372397] | Unspecified | IC50 | 1000 | Inhibition of human serum recombinant BChE after 20 mins using butyrylthiocholine iodide as a substrate by Ellman's assay [AID625547, Type: Literature] | Cholinesterase [gi:116353] |   View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | 1000 [uM] | | BioAssay | Inhibition of human serum recombinant BChE after 20 mins using butyrylthiocholine iodide as a substrate by Ellman's assay | | AID | 625547 | | BioAssay type | Literature | | Target | Cholinesterase [gi:116353] | | PubMed | 21924801 | | Data Table |  |
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| 19 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin) [AID625213, Type: other] | B2 bradykinin receptor [gi:2506481] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin) | | AID | 625213 | | BioAssay type | other | | Target | B2 bradykinin receptor [gi:2506481] | | PubMed | | | Data Table |  |
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| 20 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin) [AID625213, Type: other] | B2 bradykinin receptor [gi:2506481] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin) | | AID | 625213 | | BioAssay type | other | | Target | B2 bradykinin receptor [gi:2506481] | | PubMed | | | Data Table |  |
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| 21 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Vasopressin V1A radioligand binding (ligand: [125I] PhenylacetylTyr(Me)PheGlnAsnArgProArgTyr) [AID625233, Type: other] | Vasopressin V1a receptor [gi:586197] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Vasopressin V1A radioligand binding (ligand: [125I] PhenylacetylTyr(Me)PheGlnAsnArgProArgTyr) | | AID | 625233 | | BioAssay type | other | | Target | Vasopressin V1a receptor [gi:586197] | | PubMed | | | Data Table |  |
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| 22 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Vasopressin V1A radioligand binding (ligand: [125I] PhenylacetylTyr(Me)PheGlnAsnArgProArgTyr) [AID625233, Type: other] | Vasopressin V1a receptor [gi:586197] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Vasopressin V1A radioligand binding (ligand: [125I] PhenylacetylTyr(Me)PheGlnAsnArgProArgTyr) | | AID | 625233 | | BioAssay type | other | | Target | Vasopressin V1a receptor [gi:586197] | | PubMed | | | Data Table |  |
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| 23 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Vasopressin V1A radioligand binding (ligand: [125I] PhenylacetylTyr(Me)PheGlnAsnArgProArgTyr) [AID625233, Type: other] | Vasopressin V1a receptor [gi:586197] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Vasopressin V1A radioligand binding (ligand: [125I] PhenylacetylTyr(Me)PheGlnAsnArgProArgTyr) | | AID | 625233 | | BioAssay type | other | | Target | Vasopressin V1a receptor [gi:586197] | | PubMed | | | Data Table |  |
|
| 24 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Vascular Endothelinal Growth Factor (VEGF) radioligand binding (ligand: [125I] VEGF) [AID625231, Type: other] | Vascular endothelial growth factor receptor 1 [gi:143811474] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Vascular Endothelinal Growth Factor (VEGF) radioligand binding (ligand: [125I] VEGF) | | AID | 625231 | | BioAssay type | other | | Target | Vascular endothelial growth factor receptor 1 [gi:143811474] | | PubMed | | | Data Table |  |
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| 25 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Vascular Endothelinal Growth Factor (VEGF) radioligand binding (ligand: [125I] VEGF) [AID625231, Type: other] | Vascular endothelial growth factor receptor 1 [gi:143811474] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Vascular Endothelinal Growth Factor (VEGF) radioligand binding (ligand: [125I] VEGF) | | AID | 625231 | | BioAssay type | other | | Target | Vascular endothelial growth factor receptor 1 [gi:143811474] | | PubMed | | | Data Table |  |
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| 26 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Dopamine D2L radioligand binding (ligand: [3H] Spiperone) [AID625253, Type: other] | D(2) dopamine receptor [gi:118206] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Dopamine D2L radioligand binding (ligand: [3H] Spiperone) | | AID | 625253 | | BioAssay type | other | | Target | D(2) dopamine receptor [gi:118206] | | PubMed | | | Data Table |  |
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| 27 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Dopamine D2L radioligand binding (ligand: [3H] Spiperone) [AID625253, Type: other] | D(2) dopamine receptor [gi:118206] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Dopamine D2L radioligand binding (ligand: [3H] Spiperone) | | AID | 625253 | | BioAssay type | other | | Target | D(2) dopamine receptor [gi:118206] | | PubMed | | | Data Table |  |
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| 28 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Dopamine D2L radioligand binding (ligand: [3H] Spiperone) [AID625253, Type: other] | D(2) dopamine receptor [gi:118206] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Dopamine D2L radioligand binding (ligand: [3H] Spiperone) | | AID | 625253 | | BioAssay type | other | | Target | D(2) dopamine receptor [gi:118206] | | PubMed | | | Data Table |  |
|
| 29 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Dopamine D2L radioligand binding (ligand: [3H] Spiperone) [AID625253, Type: other] | D(2) dopamine receptor [gi:118206] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Dopamine D2L radioligand binding (ligand: [3H] Spiperone) | | AID | 625253 | | BioAssay type | other | | Target | D(2) dopamine receptor [gi:118206] | | PubMed | | | Data Table |  |
|
| 30 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Dopamine D2L radioligand binding (ligand: [3H] Spiperone) [AID625253, Type: other] | D(2) dopamine receptor [gi:118206] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Dopamine D2L radioligand binding (ligand: [3H] Spiperone) | | AID | 625253 | | BioAssay type | other | | Target | D(2) dopamine receptor [gi:118206] | | PubMed | | | Data Table |  |
|
| 31 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Dopamine D3 radioligand binding (ligand: [3H] Spiperone) [AID625254, Type: other] | D(3) dopamine receptor [gi:1169206] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [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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| 32 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Dopamine D3 radioligand binding (ligand: [3H] Spiperone) [AID625254, Type: other] | D(3) dopamine receptor [gi:1169206] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [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 |  |
|
| 33 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Dopamine D3 radioligand binding (ligand: [3H] Spiperone) [AID625254, Type: other] | D(3) dopamine receptor [gi:1169206] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [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 |  |
|
| 34 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Dopamine D3 radioligand binding (ligand: [3H] Spiperone) [AID625254, Type: other] | D(3) dopamine receptor [gi:1169206] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [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 |  |
|
| 35 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Dopamine D4.2 radioligand binding (ligand: [3H] Spiperone) [AID625255, Type: other] | D(4) dopamine receptor [gi:1345939] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Dopamine D4.2 radioligand binding (ligand: [3H] Spiperone) | | AID | 625255 | | BioAssay type | other | | Target | D(4) dopamine receptor [gi:1345939] | | PubMed | | | Data Table |  |
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| 36 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Dopamine D4.2 radioligand binding (ligand: [3H] Spiperone) [AID625255, Type: other] | D(4) dopamine receptor [gi:1345939] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Dopamine D4.2 radioligand binding (ligand: [3H] Spiperone) | | AID | 625255 | | BioAssay type | other | | Target | D(4) dopamine receptor [gi:1345939] | | PubMed | | | Data Table |  |
|
| 37 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Dopamine D4.2 radioligand binding (ligand: [3H] Spiperone) [AID625255, Type: other] | D(4) dopamine receptor [gi:1345939] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Dopamine D4.2 radioligand binding (ligand: [3H] Spiperone) | | AID | 625255 | | BioAssay type | other | | Target | D(4) dopamine receptor [gi:1345939] | | PubMed | | | Data Table |  |
|
| 38 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Endothelin ETA radioligand binding (ligand: [125I] Endothelin-1) [AID625257, Type: other] | Endothelin-1 receptor [gi:119606] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Endothelin ETA radioligand binding (ligand: [125I] Endothelin-1) | | AID | 625257 | | BioAssay type | other | | Target | Endothelin-1 receptor [gi:119606] | | PubMed | | | Data Table |  |
|
| 39 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Endothelin ETA radioligand binding (ligand: [125I] Endothelin-1) [AID625257, Type: other] | Endothelin-1 receptor [gi:119606] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Endothelin ETA radioligand binding (ligand: [125I] Endothelin-1) | | AID | 625257 | | BioAssay type | other | | Target | Endothelin-1 receptor [gi:119606] | | PubMed | | | Data Table |  |
|
| 40 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Protein Tyrosine Kinase, EGF Receptor enzyme inhibition (substrate: Poly(Glu:Tyr)) [AID625184, Type: other] | Epidermal growth factor receptor [gi:2811086] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Protein Tyrosine Kinase, EGF Receptor enzyme inhibition (substrate: Poly(Glu:Tyr)) | | AID | 625184 | | BioAssay type | other | | Target | Epidermal growth factor receptor [gi:2811086] | | PubMed | | | Data Table |  |
|
| 41 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Protein Tyrosine Kinase, EGF Receptor enzyme inhibition (substrate: Poly(Glu:Tyr)) [AID625184, Type: other] | Epidermal growth factor receptor [gi:2811086] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Protein Tyrosine Kinase, EGF Receptor enzyme inhibition (substrate: Poly(Glu:Tyr)) | | AID | 625184 | | BioAssay type | other | | Target | Epidermal growth factor receptor [gi:2811086] | | PubMed | | | Data Table |  |
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| 42 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Protein Tyrosine Kinase, EGF Receptor enzyme inhibition (substrate: Poly(Glu:Tyr)) [AID625184, Type: other] | Epidermal growth factor receptor [gi:2811086] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Protein Tyrosine Kinase, EGF Receptor enzyme inhibition (substrate: Poly(Glu:Tyr)) | | AID | 625184 | | BioAssay type | other | | Target | Epidermal growth factor receptor [gi:2811086] | | PubMed | | | Data Table |  |
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| 43 | [SID103372397] | Unspecified | | | DRUGMATRIX: Peptidase, ELA2 (Neutrophil Elastase 2) enzyme inhibition (substrate: N-MeOSuc-Ala-Ala-Pro-Val-pNA) [AID625176, Type: other] | Neutrophil elastase [gi:119292] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | BioAssay | DRUGMATRIX: Peptidase, ELA2 (Neutrophil Elastase 2) enzyme inhibition (substrate: N-MeOSuc-Ala-Ala-Pro-Val-pNA) | | AID | 625176 | | BioAssay type | other | | Target | Neutrophil elastase [gi:119292] | | PubMed | | | Data Table |  |
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| 44 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Protein Tyrosine Kinase, ERBB2 (HER2) enzyme inhibition (substrate: Poly(Glu:Tyr)) [AID625186, Type: other] | Receptor tyrosine-protein kinase erbB-2 [gi:119533] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Protein Tyrosine Kinase, ERBB2 (HER2) enzyme inhibition (substrate: Poly(Glu:Tyr)) | | AID | 625186 | | BioAssay type | other | | Target | Receptor tyrosine-protein kinase erbB-2 [gi:119533] | | PubMed | | | Data Table |  |
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| 45 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Protein Tyrosine Kinase, ERBB2 (HER2) enzyme inhibition (substrate: Poly(Glu:Tyr)) [AID625186, Type: other] | Receptor tyrosine-protein kinase erbB-2 [gi:119533] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Protein Tyrosine Kinase, ERBB2 (HER2) enzyme inhibition (substrate: Poly(Glu:Tyr)) | | AID | 625186 | | BioAssay type | other | | Target | Receptor tyrosine-protein kinase erbB-2 [gi:119533] | | PubMed | | | Data Table |  |
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| 46 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Estrogen ERalpha radioligand binding (ligand: [3H] Estradiol) [AID625258, Type: other] | Estrogen receptor [gi:544257] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Estrogen ERalpha radioligand binding (ligand: [3H] Estradiol) | | AID | 625258 | | BioAssay type | other | | Target | Estrogen receptor [gi:544257] | | PubMed | | | Data Table |  |
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| 47 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Estrogen ERalpha radioligand binding (ligand: [3H] Estradiol) [AID625258, Type: other] | Estrogen receptor [gi:544257] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Estrogen ERalpha radioligand binding (ligand: [3H] Estradiol) | | AID | 625258 | | BioAssay type | other | | Target | Estrogen receptor [gi:544257] | | PubMed | | | Data Table |  |
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| 48 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Estrogen ERalpha radioligand binding (ligand: [3H] Estradiol) [AID625258, Type: other] | Estrogen receptor [gi:544257] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Estrogen ERalpha radioligand binding (ligand: [3H] Estradiol) | | AID | 625258 | | BioAssay type | other | | Target | Estrogen receptor [gi:544257] | | PubMed | | | Data Table |  |
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| 49 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Estrogen ERalpha radioligand binding (ligand: [3H] Estradiol) [AID625258, Type: other] | Estrogen receptor [gi:544257] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Estrogen ERalpha radioligand binding (ligand: [3H] Estradiol) | | AID | 625258 | | BioAssay type | other | | Target | Estrogen receptor [gi:544257] | | PubMed | | | Data Table |  |
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| 50 | [SID103372397] | Unspecified | IC50 | | DRUGMATRIX: Protein Tyrosine Kinase, Fyn enzyme inhibition (substrate: Poly(Glu:Tyr)) [AID625185, Type: other] | Tyrosine-protein kinase Fyn [gi:125370] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 103372397 | | CID | 6112 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | DRUGMATRIX: Protein Tyrosine Kinase, Fyn enzyme inhibition (substrate: Poly(Glu:Tyr)) | | AID | 625185 | | BioAssay type | other | | Target | Tyrosine-protein kinase Fyn [gi:125370] | | PubMed | | | Data Table |  |
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