| 1 | [SID103207410] | Active | Ki | 0.00077 | Displacement of [125I]TZDM from human beta amyloid fibril 1-42 [AID308323, Type: Literature] | |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | Ki | 0.00077 [uM] | | BioAssay | Displacement of [125I]TZDM from human beta amyloid fibril 1-42 | | AID | 308323 | | BioAssay type | Literature | | Target | | | PubMed | 17544669 | | Data Table |  |
|
| 2 | [SID103207410] | Active | IC50 | 0.2 | Antihemorrhagic activity in ddY mouse assessed as inhibition of Protobothrops flavoviridis venom-induced hemorrhage incubated with compound for 10 mins measured after 24 hrs [AID592088, Type: Literature] | |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | IC50 | 0.2 [uM] | | BioAssay | Antihemorrhagic activity in ddY mouse assessed as inhibition of Protobothrops flavoviridis venom-induced hemorrhage incubated with compound for 10 mins measured after 24 hrs | | AID | 592088 | | BioAssay type | Literature | | Target | | | PubMed | 21388814 | | Data Table |  |
|
| 3 | [SID103207410] | Active | Ki | 2.4 | Inhibition of human CA2 by stopped-flow CO2 hydration assay [AID462271, Type: Literature] | Carbonic anhydrase 2 [gi:115456] |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | Ki | 2.4 [uM] | | BioAssay | Inhibition of human CA2 by stopped-flow CO2 hydration assay | | AID | 462271 | | BioAssay type | Literature | | Target | Carbonic anhydrase 2 [gi:115456] | | PubMed | 20185318 | | Data Table |  |
|
| 4 | [SID103207410] | Active | Ki | 2.89 | Inhibition of human CA1 by stopped-flow CO2 hydration assay [AID462270, Type: Literature] | Carbonic anhydrase 1 [gi:115449] |   View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | Ki | 2.89 [uM] | | BioAssay | Inhibition of human CA1 by stopped-flow CO2 hydration assay | | AID | 462270 | | BioAssay type | Literature | | Target | Carbonic anhydrase 1 [gi:115449] | | PubMed | 20185318 | | Data Table |  |
|
| 5 | [SID103207410] | Active | IC50 | 3.975 | DRUGMATRIX: Lipoxygenase 15-LO enzyme inhibition (substrate: Linoleic acid) [AID625146, Type: other] | Arachidonate 15-lipoxygenase [gi:126397] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | IC50 | 3.975 [uM] | | BioAssay | DRUGMATRIX: Lipoxygenase 15-LO enzyme inhibition (substrate: Linoleic acid) | | AID | 625146 | | BioAssay type | other | | Target | Arachidonate 15-lipoxygenase [gi:126397] | | PubMed | | | Data Table |  |
|
| 6 | [SID103207410] | Active | Ki | 7.04 | Inhibition of human CA5A by stopped-flow CO2 hydration assay [AID462274, Type: Literature] | Carbonic anhydrase 5A, mitochondrial [gi:461680] |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | Ki | 7.04 [uM] | | BioAssay | Inhibition of human CA5A by stopped-flow CO2 hydration assay | | AID | 462274 | | BioAssay type | Literature | | Target | Carbonic anhydrase 5A, mitochondrial [gi:461680] | | PubMed | 20185318 | | Data Table |  |
|
| 7 | [SID103207410] | Active | Ki | 7.41 | Inhibition of human CA7 by stopped-flow CO2 hydration assay [AID462277, Type: Literature] | Carbonic anhydrase 7 [gi:1168744] |   View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | Ki | 7.41 [uM] | | BioAssay | Inhibition of human CA7 by stopped-flow CO2 hydration assay | | AID | 462277 | | BioAssay type | Literature | | Target | Carbonic anhydrase 7 [gi:1168744] | | PubMed | 20185318 | | Data Table |  |
|
| 8 | [SID103207410] | Active | Ki | 8.45 | Inhibition of human CA6 by stopped-flow CO2 hydration assay [AID462276, Type: Literature] | Carbonic anhydrase 6 [gi:116241278] |   View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | Ki | 8.45 [uM] | | BioAssay | Inhibition of human CA6 by stopped-flow CO2 hydration assay | | AID | 462276 | | BioAssay type | Literature | | Target | Carbonic anhydrase 6 [gi:116241278] | | PubMed | 20185318 | | Data Table |  |
|
| 9 | [SID103207410] | Active | Ki | 9.43 | Inhibition of human CA14 by stopped-flow CO2 hydration assay [AID462281, Type: Literature] | Carbonic anhydrase 14 [gi:8928036] |   View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | Ki | 9.43 [uM] | | BioAssay | Inhibition of human CA14 by stopped-flow CO2 hydration assay | | AID | 462281 | | BioAssay type | Literature | | Target | Carbonic anhydrase 14 [gi:8928036] | | PubMed | 20185318 | | Data Table |  |
|
| 10 | [SID103207410] | Active | Ki | 9.78 | Inhibition of human CA12 by stopped-flow CO2 hydration assay [AID462279, Type: Literature] | Carbonic anhydrase 12 [gi:5915866] |   View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | Ki | 9.78 [uM] | | BioAssay | Inhibition of human CA12 by stopped-flow CO2 hydration assay | | AID | 462279 | | BioAssay type | Literature | | Target | Carbonic anhydrase 12 [gi:5915866] | | PubMed | 20185318 | | Data Table |  |
|
| 11 | [SID103207410] | Active | Ki | 9.87 | Inhibition of human CA9 by stopped-flow CO2 hydration assay [AID462278, Type: Literature] | Carbonic anhydrase 9 [gi:83300925] |   View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | Ki | 9.87 [uM] | | BioAssay | Inhibition of human CA9 by stopped-flow CO2 hydration assay | | AID | 462278 | | BioAssay type | Literature | | Target | Carbonic anhydrase 9 [gi:83300925] | | PubMed | 20185318 | | Data Table |  |
|
| 12 | [SID103207410] | Active | Ki | 10.5 | Inhibition of human CA5B by stopped-flow CO2 hydration assay [AID462275, Type: Literature] | Carbonic anhydrase 5B, mitochondrial [gi:8928041] |   View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | Ki | 10.5 [uM] | | BioAssay | Inhibition of human CA5B by stopped-flow CO2 hydration assay | | AID | 462275 | | BioAssay type | Literature | | Target | Carbonic anhydrase 5B, mitochondrial [gi:8928041] | | PubMed | 20185318 | | Data Table |  |
|
| 13 | [SID103207410] | Active | Ki | 10.8 | Inhibition of human CA4 by stopped-flow CO2 hydration assay [AID462273, Type: Literature] | Carbonic anhydrase 4 [gi:115465] |   View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | Ki | 10.8 [uM] | | BioAssay | Inhibition of human CA4 by stopped-flow CO2 hydration assay | | AID | 462273 | | BioAssay type | Literature | | Target | Carbonic anhydrase 4 [gi:115465] | | PubMed | 20185318 | | Data Table |  |
|
| 14 | [SID103207410] | Active | Ki | 11.1 | Inhibition of human CA3 by stopped-flow CO2 hydration assay [AID462272, Type: Literature] | Carbonic anhydrase 3 [gi:134047703] |   View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | Ki | 11.1 [uM] | | BioAssay | Inhibition of human CA3 by stopped-flow CO2 hydration assay | | AID | 462272 | | BioAssay type | Literature | | Target | Carbonic anhydrase 3 [gi:134047703] | | PubMed | 20185318 | | Data Table |  |
|
| 15 | [SID103207410] | Active | Ki | 12.2 | Inhibition of mouse CA13 by stopped-flow CO2 hydration assay [AID462280, Type: Literature] | Carbonic anhydrase 13 [gi:30580372] |   View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | Ki | 12.2 [uM] | | BioAssay | Inhibition of mouse CA13 by stopped-flow CO2 hydration assay | | AID | 462280 | | BioAssay type | Literature | | Target | Carbonic anhydrase 13 [gi:30580372] | | PubMed | 20185318 | | Data Table |  |
|
| 16 | [SID47193700] | Active | | | HTS-Luminescent assay for inhibitors of ALR by detection of hydrogen peroxide production Measured in Biochemical System Using Plate Reader - 2036-02_Inhibitor_SinglePoint_HTS [AID485317, Type: screening] | FAD-linked sulfhydryl oxidase ALR [Homo sapiens] [gi:54112432] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 47193700 | | CID | 445858 | | Outcome | Active | | BioAssay | HTS-Luminescent assay for inhibitors of ALR by detection of hydrogen peroxide production Measured in Biochemical System Using Plate Reader - 2036-02_Inhibitor_SinglePoint_HTS | | AID | 485317 | | BioAssay type | screening | | Target | FAD-linked sulfhydryl oxidase ALR [Homo sapiens] [gi:54112432] | | PubMed | | | Data Table |  |
|
| 17 | [SID103207410] | Active | | | Binding affinity to amyloid beta (1 to 42) fibrils by change in fluorescence at 100 uM after 10 mins [AID475504, Type: Literature] | |   View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | BioAssay | Binding affinity to amyloid beta (1 to 42) fibrils by change in fluorescence at 100 uM after 10 mins | | AID | 475504 | | BioAssay type | Literature | | Target | | | PubMed | 19640715 | | Data Table |  |
|
| 18 | [SID103207410] | Active | | | Binding affinity to amyloid beta (1 to 42) oligomers by change in fluorescence at 100 uM after 10 mins [AID475505, Type: Literature] | |   View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | BioAssay | Binding affinity to amyloid beta (1 to 42) oligomers by change in fluorescence at 100 uM after 10 mins | | AID | 475505 | | BioAssay type | Literature | | Target | | | PubMed | 19640715 | | Data Table |  |
|
| 19 | [SID103207410] | Active | | | Antioxidant activity assessed as DPPH scavenging activity [AID399080, Type: Literature] | |   View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | BioAssay | Antioxidant activity assessed as DPPH scavenging activity | | AID | 399080 | | BioAssay type | Literature | | Target | | | PubMed | 16309309 | | Data Table |  |
|
| 20 | [SID103207410] | Active | | | Antihyperglycemic activity in po dosed diabetic KK-Ay mouse model [AID592241, Type: Literature] | |   View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | BioAssay | Antihyperglycemic activity in po dosed diabetic KK-Ay mouse model | | AID | 592241 | | BioAssay type | Literature | | Target | | | PubMed | 20879744 | | Data Table |  |
|
| 21 | [SID103207410] | Active | | | Hypoglycemic activity in rat assessed as decrease in plasma glucose at 5 mg/kg, iv [AID592242, Type: Literature] | |   View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | BioAssay | Hypoglycemic activity in rat assessed as decrease in plasma glucose at 5 mg/kg, iv | | AID | 592242 | | BioAssay type | Literature | | Target | | | PubMed | 20879744 | | Data Table |  |
|
| 22 | [SID103207410] | Active | | | Hypoglycemic activity in rat assessed as increase in insulin concentration at 5 mg/kg, iv [AID592243, Type: Literature] | |   View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Active | | BioAssay | Hypoglycemic activity in rat assessed as increase in insulin concentration at 5 mg/kg, iv | | AID | 592243 | | BioAssay type | Literature | | Target | | | PubMed | 20879744 | | Data Table |  |
|
| 23 | [SID57264356] | Active | | | Luminescence-based cell-based primary high throughput screening assay to identify activators of the GAA850 frataxin (FXN) promoter [AID540364, Type: screening] | |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 57264356 | | CID | 445858 | | Outcome | Active | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify activators of the GAA850 frataxin (FXN) promoter | | AID | 540364 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 24 | [SID103207410] | Unspecified | IC50 | 68 | Cytotoxicity against human OE21 cells after 72 hrs by MTT assay [AID607594, Type: Literature] | |   View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | IC50 | 68 [uM] | | BioAssay | Cytotoxicity against human OE21 cells after 72 hrs by MTT assay | | AID | 607594 | | BioAssay type | Literature | | Target | | | PubMed | 21696954 | | Data Table |  |
|
| 25 | [SID103207410] | Unspecified | IC50 | 95 | Cytotoxicity against human LoVo cells after 72 hrs by MTT assay [AID607598, Type: Literature] | |   View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | IC50 | 95 [uM] | | BioAssay | Cytotoxicity against human LoVo cells after 72 hrs by MTT assay | | AID | 607598 | | BioAssay type | Literature | | Target | | | PubMed | 21696954 | | Data Table |  |
|
| 26 | [SID103207410] | Unspecified | IC50 | 100 | Cytotoxicity against human U373 cells after 72 hrs by MTT assay [AID607593, Type: Literature] | |   View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | IC50 | 100 [uM] | | BioAssay | Cytotoxicity against human U373 cells after 72 hrs by MTT assay | | AID | 607593 | | BioAssay type | Literature | | Target | | | PubMed | 21696954 | | Data Table |  |
|
| 27 | [SID103207410] | Unspecified | IC50 | 100 | Cytotoxicity against human A549 cells after 72 hrs by MTT assay [AID607595, Type: Literature] | |   View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | IC50 | 100 [uM] | | BioAssay | Cytotoxicity against human A549 cells after 72 hrs by MTT assay | | AID | 607595 | | BioAssay type | Literature | | Target | | | PubMed | 21696954 | | Data Table |  |
|
| 28 | [SID103207410] | Unspecified | IC50 | 100 | Cytotoxicity against human PC3 cells after 72 hrs by MTT assay [AID607596, Type: Literature] | |   View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | IC50 | 100 [uM] | | BioAssay | Cytotoxicity against human PC3 cells after 72 hrs by MTT assay | | AID | 607596 | | BioAssay type | Literature | | Target | | | PubMed | 21696954 | | Data Table |  |
|
| 29 | [SID103207410] | Unspecified | IC50 | 100 | Cytotoxicity against human SK-MEL-28 cells after 72 hrs by MTT assay [AID607597, Type: Literature] | |   View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | IC50 | 100 [uM] | | BioAssay | Cytotoxicity against human SK-MEL-28 cells after 72 hrs by MTT assay | | AID | 607597 | | BioAssay type | Literature | | Target | | | PubMed | 21696954 | | Data Table |  |
|
| 30 | [SID103207410] | Unspecified | IC50 | 100 | Inhibition of HIV1 integrase by ELISA [AID371216, Type: Literature] | |   View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | IC50 | 100 [uM] | | BioAssay | Inhibition of HIV1 integrase by ELISA | | AID | 371216 | | BioAssay type | Literature | | Target | | | PubMed | 18952420 | | Data Table |  |
|
| 31 | [SID103207410] | Unspecified | IC50 | 100 | Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method [AID635414, Type: Literature] | Acetylcholinesterase [gi:14916521] |   View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | IC50 | 100 [uM] | | BioAssay | Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method | | AID | 635414 | | BioAssay type | Literature | | Target | Acetylcholinesterase [gi:14916521] | | PubMed | 22041172 | | Data Table |  |
|
| 32 | [SID103207410] | Unspecified | IC50 | 111.6 | Antioxidant activity assessed as residual DPPH radical scavenging activity after 45 mins by spectrophotometrically [AID568834, Type: Literature] | |   View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | IC50 | 111.6 [uM] | | BioAssay | Antioxidant activity assessed as residual DPPH radical scavenging activity after 45 mins by spectrophotometrically | | AID | 568834 | | BioAssay type | Literature | | Target | | | PubMed | 21216503 | | Data Table |  |
|
| 33 | [SID103207410] | Unspecified | EC50 | 250 | Antioxidant activity assessed as DPPH radical scavenging activity by spectrophotometry [AID590194, Type: Literature] | |   View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | EC50 | 250 [uM] | | BioAssay | Antioxidant activity assessed as DPPH radical scavenging activity by spectrophotometry | | AID | 590194 | | BioAssay type | Literature | | Target | | | PubMed | 21377874 | | Data Table |  |
|
| 34 | [SID103207410] | Unspecified | IC50 | 350 | Inhibition of mushroom tyrosinase after 25 mins by spectrophotometry [AID590195, Type: Literature] | Polyphenol oxidase 2 [gi:6686057] |   View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | IC50 | 350 [uM] | | BioAssay | Inhibition of mushroom tyrosinase after 25 mins by spectrophotometry | | AID | 590195 | | BioAssay type | Literature | | Target | Polyphenol oxidase 2 [gi:6686057] | | PubMed | 21377874 | | Data Table |  |
|
| 35 | [SID103207410] | Unspecified | IC50 | 1000 | Cytotoxicity against human K562 cells after 5 days by XTT assay [AID312292, Type: Literature] | |   View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | IC50 | 1000 [uM] | | BioAssay | Cytotoxicity against human K562 cells after 5 days by XTT assay | | AID | 312292 | | BioAssay type | Literature | | Target | | | PubMed | 18076140 | | Data Table |  |
|
| 36 | [SID103207410] | Unspecified | IC50 | 2000 | Inhibition of hyaluronidase [AID477408, Type: Literature] | |   View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | IC50 | 2000 [uM] | | BioAssay | Inhibition of hyaluronidase | | AID | 477408 | | BioAssay type | Literature | | Target | | | PubMed | 20184336 | | Data Table |  |
|
| 37 | [SID103207410] | Unspecified | | | Cytotoxicity against human PANC1 cells in nutrient-deprived condition assessed as preferential cell death after 24 hrs by trypan blue dye exclusion method [AID477928, Type: Literature] | |   View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Cytotoxicity against human PANC1 cells in nutrient-deprived condition assessed as preferential cell death after 24 hrs by trypan blue dye exclusion method | | AID | 477928 | | BioAssay type | Literature | | Target | | | PubMed | 20307087 | | Data Table |  |
|
| 38 | [SID103207410] | Unspecified | | | Antioxidant activity assessed as formazan formation induced absorbance changes at 25 ppm at 570 nm at 37 degC for 6 hrs by MTT assay [AID492140, Type: Literature] | |   View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Antioxidant activity assessed as formazan formation induced absorbance changes at 25 ppm at 570 nm at 37 degC for 6 hrs by MTT assay | | AID | 492140 | | BioAssay type | Literature | | Target | | | PubMed | 20565070 | | Data Table |  |
|
| 39 | [SID103207410] | Unspecified | | | Redox potential at pH 7.3 by differential pulse and cyclic voltametry [AID499282, Type: Literature] | |   View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Redox potential at pH 7.3 by differential pulse and cyclic voltametry | | AID | 499282 | | BioAssay type | Literature | | Target | | | PubMed | 20650639 | | Data Table |  |
|
| 40 | [SID103207410] | Unspecified | | | Antioxidant activity assessed as inhibition of AAPH-induced lipid peroxidation in liposomes measured as Trolox equivalent antioxidant capacity [AID499283, Type: Literature] | |   View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Antioxidant activity assessed as inhibition of AAPH-induced lipid peroxidation in liposomes measured as Trolox equivalent antioxidant capacity | | AID | 499283 | | BioAssay type | Literature | | Target | | | PubMed | 20650639 | | Data Table |  |
|
| 41 | [SID103207410] | Unspecified | | | Antiinflammatory activity in CD1 mouse assessed as inhibition of croton oil-induced ear oedema at 0.3 umol/cm^2 after 6 hrs [AID309363, Type: Literature] | |   View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Antiinflammatory activity in CD1 mouse assessed as inhibition of croton oil-induced ear oedema at 0.3 umol/cm^2 after 6 hrs | | AID | 309363 | | BioAssay type | Literature | | Target | | | PubMed | 17768049 | | Data Table |  |
|
| 42 | [SID103207410] | Unspecified | | | Cell viability in TPA-induced superoxide (O2-) generation in human promyelocytic leukemia HL-60 cells, at 100 uM concentration [AID82003, Type: Literature] | |   View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Cell viability in TPA-induced superoxide (O2-) generation in human promyelocytic leukemia HL-60 cells, at 100 uM concentration | | AID | 82003 | | BioAssay type | Literature | | Target | | | PubMed | 10888327 | | Data Table |  |
|
| 43 | [SID103207410] | Unspecified | | | Inhibitory activity against TPA-induced superoxide (O2-) generation in human promyelocytic leukemia HL-60 cells, at 100 uM concentration [AID82327, Type: Literature] | |   View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Inhibitory activity against TPA-induced superoxide (O2-) generation in human promyelocytic leukemia HL-60 cells, at 100 uM concentration | | AID | 82327 | | BioAssay type | Literature | | Target | | | PubMed | 10888327 | | Data Table |  |
|
| 44 | [SID103207410] | Unspecified | | | Inhibition of HDAC in human Hela cells nuclear extracts assessed as residual activity at 500 uM by fluorimetric assay [AID447578, Type: Literature] | |   View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Inhibition of HDAC in human Hela cells nuclear extracts assessed as residual activity at 500 uM by fluorimetric assay | | AID | 447578 | | BioAssay type | Literature | | Target | | | PubMed | 19520580 | | Data Table |  |
|
| 45 | [SID103207410] | Unspecified | | | Antioxidant activity assessed as trolox equivalents of ABTS radical scavenging activity by TEAC assay [AID568835, Type: Literature] | |   View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Antioxidant activity assessed as trolox equivalents of ABTS radical scavenging activity by TEAC assay | | AID | 568835 | | BioAssay type | Literature | | Target | | | PubMed | 21216503 | | Data Table |  |
|
| 46 | [SID103207410] | Unspecified | | | Inhibition of theophylline-stimulated melanogenesis in mouse B16-4A5 cells at 30 uM after 72 hrs [AID462333, Type: Literature] | |   View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Inhibition of theophylline-stimulated melanogenesis in mouse B16-4A5 cells at 30 uM after 72 hrs | | AID | 462333 | | BioAssay type | Literature | | Target | | | PubMed | 20189399 | | Data Table |  |
|
| 47 | [SID103207410] | Unspecified | | | Toxicity in mouse B16-4A5 cells assessed as inhibition of cell proliferation at 30 uM in presence of 1 mM theophylline after 72 hrs by WST8 dye reduction assay [AID462342, Type: Literature] | |   View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Toxicity in mouse B16-4A5 cells assessed as inhibition of cell proliferation at 30 uM in presence of 1 mM theophylline after 72 hrs by WST8 dye reduction assay | | AID | 462342 | | BioAssay type | Literature | | Target | | | PubMed | 20189399 | | Data Table |  |
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| 48 | [SID103207410] | Unspecified | | | Hypoglycemic activity in rat L6 myotubes assessed as increase in 2-deoxyglucose transport at 25 uM relative to control [AID592244, Type: Literature] | |   View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Hypoglycemic activity in rat L6 myotubes assessed as increase in 2-deoxyglucose transport at 25 uM relative to control | | AID | 592244 | | BioAssay type | Literature | | Target | | | PubMed | 20879744 | | Data Table |  |
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| 49 | [SID103207410] | Unspecified | | | Antioxidant activity assessed as trolox equivalents by ORAC-fluorescence assay [AID331670, Type: Literature] | |   View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Antioxidant activity assessed as trolox equivalents by ORAC-fluorescence assay | | AID | 331670 | | BioAssay type | Literature | | Target | | | PubMed | 18406135 | | Data Table |  |
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| 50 | [SID103207410] | Unspecified | | | Inhibition of bovine thymocytes protein tyrosine kinase assessed as angiotensin 1 phosphorylation [AID336952, Type: other] | |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 103207410 | | CID | 445858 | | Outcome | Unspecified | | BioAssay | Inhibition of bovine thymocytes protein tyrosine kinase assessed as angiotensin 1 phosphorylation | | AID | 336952 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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