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259089-67-3 靶点实验数据

HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:Center for Chemical Genomics, University of Michigan 靶标:N/A
External ID: TargetID_659_CEMA
Protocol: Black, standard capacity streptavidin-coated 384-well plates (Pierce 15407) were first washed with 50 L of phosphate buffer (100 mM, pH 7.0; PB7) three times using a Biotek 405 ELX plate washer. Subsequently, 5 L of biotinylated pre-miRNA substrate (500 nM final) was dispensed into the plate using a Multidrop Combi Reagent Dispenser (Thermo Scientific). Plates were then centrifuged for 1 min at 1,000 RPM (223 g), sealed with plate tape, and incubated overnight at 4 C. The following morning, plates were washed three times with 50 L of PB7, followed by the addition of 5 L of Dicer digest buffer (20 mM Tris, 12 mM NaCl, 2.5 mM MgCl2, 1 mM fresh DTT, and 4.5% DMSO) and centrifugation. Compounds (50 nL of 5 mM DMSO stock, 25 M final) were then added into the sample wells using a Sciclone (Caliper) liquid handler with V&P pintool; the same volume of DMSO was added to the control wells. The plates were incubated at 25 C for 15 min before addition of 5 L of digest buffer containing 217 g/nL Dicer (108 g/mL Dicer, 5% glycerol and 0.01% Triton X-100 final, excess with respect to pre-miRNA). For the positive control wells, digest buffer without Dicer was added. The plates were centrifuged again and resealed before being placed in a 37 C incubator for 5 h. After Dicer cleavage, plates were washed three times with 50 L of PB7. mTet-HRP in PB7 (10 L, 750 nM final) was then dispensed into each well. The plates were subsequently centrifuged, sealed, and incubated at 25 C for 2 h. Plates were then washed three times with 50 L of wash buffer (2 mM imidazole, 260 mM NaCl, 0.5 mM EDTA, 0.1% Tween-20, pH 7.0), followed by washing three additional times with 50 L of PB7. Finally, SuperSignal West Pico (25 L; Pierce) was added, the plates were incubated at 25 C for 5 min, and chemiluminescence signal was detected using a PHERAstar plate reader using LUM plus module (BMG Labtech).
Comment: The activity outcome is based on a Z-score (number of standard deviations from the negative control mean) of 3 or higher on at least 50% times that the sample was screened.

For instance, if the sample was screened in n=4 runs, it would be considered active only if it had a Z-score of 3 or above in at least 2 runs.
Z_SCORE
2.91
-0.56
0.61
2.15
0.54
-0.32
1.12
-0.07
0.61
1.55
-0.77
-0.76
-2.08
0.67
-0.35
0.17
-1.42
-0.64
-5.35
1.42
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:Center for Chemical Genomics, University of Michigan 靶标:
External ID: MScreen:TargetID_600
Protocol: C-terminally 6xHis tagged CDK2/Cyclin A complex and N-terminally Flag tagged CDC25B C473S (372-566) were expressed and purified. Proteins were incubated together at a final concentration of 125 nM each for 1 hr prior to incubation with compound for 1 hr, followed by addition of anti-6xHis europium cryptate donor beads (Cisbio) and anti-Flag XL-665 acceptor beads (Cisbio) at a final dilution of 1:350 for 1 hr. 20mM potassium fluoride was added 10 minute prior to plate reading. Assay reagents were dispensed using a multidrop liquid dispenser (Thermo Scientific) onto uncoated, black, low-volume, 384-well plates (Corning). Assay plates were quantified using an Envision plate reader (Perkin-Elmer) with excitation of the europium crytate donor at 337 nm wavelength and emission of the donor at 620 nm and emission of the XL-665 acceptor at 665 nm in 18 uL volumes. Assays were performed in a buffer containing 50 mM Tris (pH 7.5), 50 mM NaCl, 10mM MgCl2, 1mM TCEP, with addition of and 1mM ATP, 0.05% BSA, and 0.05% Tween-20 immediately prior to the start of the assay.
Comment: The activity outcome is based on a Z-score (number of standard deviations from the negative control mean) of 3 or higher on at least 50% times that the sample was screened.
For instance, if the sample was screened in n=4 runs, it would be considered active only if it had a Z-score of 3 or above in at least 2 runs.

This screen was funded by NIH grant number: R01CA181185
Z_SCORE
0.28
-0.54
-0.02
0.22
0.37
-0.81
-0.26
-0.14
-0.61
-0.44
0.29
0.22
-0.12
-0.13
0.95
-0.29
-0.37
0.17
-0.64
-0.78
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:HepG2-CD81
External ID: CHEMBL4483864
Protocol: N/A
Comment: Compounds with activity <= 10uM or explicitly reported as active by ChEMBL are flagged as active in this PubChem assay presentation.

Journal: Science
Year: 2018
Volume: 362
Issue: 6419
DOI: 10.1126/science.aat9446

Target ChEMBL ID: CHEMBL4543887
ChEMBL Target Name: HepG2-CD81
ChEMBL Target Type: CELL-LINE - Target is a specific cell-line
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular

Data Source: Winzeler Lab Plasmodium Screening
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard Units
3.48HEPG2TOX ASSAY - CC90=3.48uM
1.05HEPG2TOX ASSAY - CC50=1.05uM
1.05HEPG2TOX ASSAY - CC90=1.05uM
6.54HEPG2TOX ASSAY - CC50=6.54uM
4.75HEPG2TOX ASSAY - CC90=4.75uM
1.63HEPG2TOX ASSAY - CC50=1.63uM
1.63HEPG2TOX ASSAY - CC90=1.63uM
7.48HEPG2TOX ASSAY - CC50=7.48uM
3.26HEPG2TOX ASSAY - CC90=3.26uM
0.0189HEPG2TOX ASSAY - CC50=0.0189uM
6.77HEPG2TOX ASSAY - CC90=6.77uM
7.54HEPG2TOX ASSAY - CC50=7.54uM
12.4HEPG2TOX ASSAY - CC90>12.4uM
6.3HEPG2TOX ASSAY - CC50=6.3uM
6.3HEPG2TOX ASSAY - CC90=6.3uM
9.05HEPG2TOX ASSAY - CC50=9.05uM
14.9HEPG2TOX ASSAY - CC90>14.9uM
12.7HEPG2TOX ASSAY - CC50>12.7uM
12.7HEPG2TOX ASSAY - CC90>12.7uM
8.37HEPG2TOX ASSAY - CC50>8.37uM
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Plasmodium berghei
External ID: CHEMBL4483863
Protocol: N/A
Comment: Compounds with activity <= 10uM or explicitly reported as active by ChEMBL are flagged as active in this PubChem assay presentation.

Journal: Science
Year: 2018
Volume: 362
Issue: 6419
DOI: 10.1126/science.aat9446

Target ChEMBL ID: CHEMBL612653
ChEMBL Target Name: Plasmodium berghei
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular

Data Source: Winzeler Lab Plasmodium Screening
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard Units
9.56LUCIFERASE EXPRESSION CONTROL - IC90>9.56uM
1.17LUCIFERASE INFECTION ASSAY - IC50=1.17uM
1.41LUCIFERASE INFECTION ASSAY - IC90=1.41uM
10LUCIFERASE EXPRESSION CONTROL - IC50>10uM
9.72LUCIFERASE EXPRESSION CONTROL - IC90>9.72uM
9.01LUCIFERASE INFECTION ASSAY - IC50>9.01uM
9.01LUCIFERASE INFECTION ASSAY - IC90>9.01uM
9.01LUCIFERASE EXPRESSION CONTROL - IC50>9.01uM
9.01LUCIFERASE EXPRESSION CONTROL - IC90>9.01uM
8.99LUCIFERASE INFECTION ASSAY - IC50=8.99uM
10LUCIFERASE INFECTION ASSAY - IC90>10uM
10LUCIFERASE EXPRESSION CONTROL - IC50>10uM
9.81LUCIFERASE EXPRESSION CONTROL - IC90>9.81uM
3.23LUCIFERASE INFECTION ASSAY - IC50=3.23uM
6.33LUCIFERASE INFECTION ASSAY - IC90>6.33uM
6.33LUCIFERASE EXPRESSION CONTROL - IC50>6.33uM
8.74LUCIFERASE EXPRESSION CONTROL - IC90>8.74uM
10LUCIFERASE INFECTION ASSAY - IC50>10uM
10LUCIFERASE INFECTION ASSAY - IC90>10uM
10LUCIFERASE EXPRESSION CONTROL - IC50>10uM