| 1 | [SID103178965] | Active | Kd | 0.12 | Ability to enhance the binding of (+/-)-[3H]nicotine to the rat brain P2 fraction at binding site 2 [AID30389, Type: Literature] | |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103178965 | | CID | 8082 | | Outcome | Active | | Kd | 0.12 [uM] | | BioAssay | Ability to enhance the binding of (+/-)-[3H]nicotine to the rat brain P2 fraction at binding site 2 | | AID | 30389 | | BioAssay type | Literature | | Target | | | PubMed | 4032427 | | Data Table |  |
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| 2 | [SID103178965] | Unspecified | Kd | 69 | Ability to enhance the binding of (+/-)-[3H]nicotine to the rat brain P2 fraction at binding site 3. [AID30391, Type: Literature] | |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103178965 | | CID | 8082 | | Outcome | Unspecified | | Kd | 69 [uM] | | BioAssay | Ability to enhance the binding of (+/-)-[3H]nicotine to the rat brain P2 fraction at binding site 3. | | AID | 30391 | | BioAssay type | Literature | | Target | | | PubMed | 4032427 | | Data Table |  |
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| 3 | [SID103178965] | Unspecified | Ki | 54000 | Inhibition of human PAT1-mediated L-[3H]proline uptake in human Caco2 cells after 10 mins by liquid scintillation counting [AID630741, Type: Literature] | |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103178965 | | CID | 8082 | | Outcome | Unspecified | | Ki | 54000 [uM] | | BioAssay | Inhibition of human PAT1-mediated L-[3H]proline uptake in human Caco2 cells after 10 mins by liquid scintillation counting | | AID | 630741 | | BioAssay type | Literature | | Target | | | PubMed | 21955456 | | Data Table |  |
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| 4 | [SID103178965] | Unspecified | | | Inhibition of Thromboxane synthetase at 100 uM [AID213129, Type: Literature] | Thromboxane-A synthase [gi:254763392] |   View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103178965 | | CID | 8082 | | Outcome | Unspecified | | BioAssay | Inhibition of Thromboxane synthetase at 100 uM | | AID | 213129 | | BioAssay type | Literature | | Target | Thromboxane-A synthase [gi:254763392] | | PubMed | 7199089 | | Data Table |  |
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| 5 | [SID103178965] | Unspecified | | | Compounds was evaluated for their ability to enhance (+/-)-[3H]nicotine binding at a dose range 10 E -9 - 10 E -6 M was reported [AID30528, Type: Literature] | |   View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 103178965 | | CID | 8082 | | Outcome | Unspecified | | BioAssay | Compounds was evaluated for their ability to enhance (+/-)-[3H]nicotine binding at a dose range 10 E -9 - 10 E -6 M was reported | | AID | 30528 | | BioAssay type | Literature | | Target | | | PubMed | 4032427 | | Data Table |  |
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| 6 | [SID103178965] | Unspecified | | | Dissociation constant, pKa of the compound [AID342464, Type: Literature] | |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 103178965 | | CID | 8082 | | Outcome | Unspecified | | BioAssay | Dissociation constant, pKa of the compound | | AID | 342464 | | BioAssay type | Literature | | Target | | | PubMed | 18570365 | | Data Table |  |
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| 7 | [SID103178965] | Unspecified | | | Association constant was determined [AID25336, Type: Literature] | |   View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 103178965 | | CID | 8082 | | Outcome | Unspecified | | BioAssay | Association constant was determined | | AID | 25336 | | BioAssay type | Literature | | Target | | | PubMed | 15026074 | | Data Table |  |
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| 8 | [SID103178965] | Unspecified | | | Maximum percent of enhancement of binding. [AID30377, Type: Literature] | |   View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 103178965 | | CID | 8082 | | Outcome | Unspecified | | BioAssay | Maximum percent of enhancement of binding. | | AID | 30377 | | BioAssay type | Literature | | Target | | | PubMed | 4032427 | | Data Table |  |
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| 9 | [SID103178965] | Unspecified | | | Maximum percent of inhibition of binding was determined [AID30378, Type: Literature] | |   View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103178965 | | CID | 8082 | | Outcome | Unspecified | | BioAssay | Maximum percent of inhibition of binding was determined | | AID | 30378 | | BioAssay type | Literature | | Target | | | PubMed | 4032427 | | Data Table |  |
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| 10 | [SID103178965] | Unspecified | | | Compound was evaluated for ability to enhance the binding of (+/-)-[3H]nicotine to the rat brain P2 fraction at binding site 1; 10e-9-10e-6 [AID30386, Type: Literature] | |   View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103178965 | | CID | 8082 | | Outcome | Unspecified | | BioAssay | Compound was evaluated for ability to enhance the binding of (+/-)-[3H]nicotine to the rat brain P2 fraction at binding site 1; 10e-9-10e-6 | | AID | 30386 | | BioAssay type | Literature | | Target | | | PubMed | 4032427 | | Data Table |  |
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| 11 | [SID48414344] | Inactive | | | DSSTox (CPDBAS) Carcinogenic Potency Database Summary Rat Bioassay Results [AID1208, Type: other] | |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 48414344 | | CID | 8082 | | Outcome | Inactive | | BioAssay | DSSTox (CPDBAS) Carcinogenic Potency Database Summary Rat Bioassay Results | | AID | 1208 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 12 | [SID48414344] | Inactive | | | DSSTox (CPDBAS) Carcinogenic Potency Database Summary MultiCellCall Results [AID1205, Type: other] | |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 48414344 | | CID | 8082 | | Outcome | Inactive | | BioAssay | DSSTox (CPDBAS) Carcinogenic Potency Database Summary MultiCellCall Results | | AID | 1205 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 13 | [SID48414344] | Inactive | | | DSSTox (CPDBAS) Carcinogenic Potency Database Summary SingleCellCall Results [AID1189, Type: other] | |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 48414344 | | CID | 8082 | | Outcome | Inactive | | BioAssay | DSSTox (CPDBAS) Carcinogenic Potency Database Summary SingleCellCall Results | | AID | 1189 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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