| 1 | [SID103312988] | Active | IC50 | 0.026 | Inhibition of human adenosine kinase activity [AID33990, Type: Literature] | |   View X | Row No. | 1 | | Structure | 
| | Substance | | | SID | 103312988 | | CID | 97297 | | Outcome | Active | | IC50 | 0.026 [uM] | | BioAssay | Inhibition of human adenosine kinase activity | | AID | 33990 | | BioAssay type | Literature | | Target | | | PubMed | 11958989 | | Data Table | |
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| 2 | [SID103312988] | Active | IC50 | 0.026 | Inhibition of recombinant human adenosine kinase [AID33985, Type: Literature] | | View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103312988 | | CID | 97297 | | Outcome | Active | | IC50 | 0.026 [uM] | | BioAssay | Inhibition of recombinant human adenosine kinase | | AID | 33985 | | BioAssay type | Literature | | Target | | | PubMed | 10956196 | | Data Table | |
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| 3 | [SID103312988] | Active | IC50 | 0.026 | Inhibitory activity against human recombinant adenosine kinase [AID33984, Type: Literature] | | View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103312988 | | CID | 97297 | | Outcome | Active | | IC50 | 0.026 [uM] | | BioAssay | Inhibitory activity against human recombinant adenosine kinase | | AID | 33984 | | BioAssay type | Literature | | Target | | | PubMed | 14561094 | | Data Table | |
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| 4 | [SID103312988] | Active | IC50 | 0.026 | Inhibitory concentration against human recombinant adenosine kinase using [14C]AMP as radioligand [AID255140, Type: Literature] | Adenosine kinase [gi:6840802] | View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103312988 | | CID | 97297 | | Outcome | Active | | IC50 | 0.026 [uM] | | BioAssay | Inhibitory concentration against human recombinant adenosine kinase using [14C]AMP as radioligand | | AID | 255140 | | BioAssay type | Literature | | Target | Adenosine kinase [gi:6840802] | | PubMed | 16190769 | | Data Table | |
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| 5 | [SID103312988] | Active | Ki | 0.03 | Inhibition of adhenosine kinase [AID325840, Type: Literature] | | View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 103312988 | | CID | 97297 | | Outcome | Active | | Ki | 0.03 [uM] | | BioAssay | Inhibition of adhenosine kinase | | AID | 325840 | | BioAssay type | Literature | | Target | | | PubMed | 18077363 | | Data Table | |
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| 6 | [SID103312988] | Active | IC50 | | Inhibition of ERK2 [AID325563, Type: Literature] | | View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 103312988 | | CID | 97297 | | Outcome | Active | | IC50 | [uM] | | BioAssay | Inhibition of ERK2 | | AID | 325563 | | BioAssay type | Literature | | Target | | | PubMed | 18077363 | | Data Table | |
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| 7 | [SID103312988] | Unspecified | IC50 | 229.087 | Binding affinity to ENT1 transporter [AID330912, Type: Literature] | | View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 103312988 | | CID | 97297 | | Outcome | Unspecified | | IC50 | 229.087 [uM] | | BioAssay | Binding affinity to ENT1 transporter | | AID | 330912 | | BioAssay type | Literature | | Target | | | PubMed | 18289860 | | Data Table | |
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| 8 | [SID103312988] | Unspecified | | | Inhibition of adenosine kinase [AID382097, Type: Literature] | | View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 103312988 | | CID | 97297 | | Outcome | Unspecified | | BioAssay | Inhibition of adenosine kinase | | AID | 382097 | | BioAssay type | Literature | | Target | | | PubMed | 18359230 | | Data Table | |
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| 9 | [SID103312988] | Unspecified | | | Inhibition concentration against human adenosine kinase [AID33993, Type: Literature] | | View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103312988 | | CID | 97297 | | Outcome | Unspecified | | BioAssay | Inhibition concentration against human adenosine kinase | | AID | 33993 | | BioAssay type | Literature | | Target | | | PubMed | 11958989 | | Data Table | |
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| 10 | [SID103312988] | Unspecified | | | Evaluated for antiseizure activity in rat maximal electric shock (MES) seizure model and represented as ED50. [AID176394, Type: Literature] | | View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103312988 | | CID | 97297 | | Outcome | Unspecified | | BioAssay | Evaluated for antiseizure activity in rat maximal electric shock (MES) seizure model and represented as ED50. | | AID | 176394 | | BioAssay type | Literature | | Target | | | PubMed | 10956196 | | Data Table | |
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Chemical Probe 
Active 
Inactive 
Inconclusive 
Unspecified 
