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Assay Detail

CHEMBL5733723

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Biological Assays: Assays are conducted in 1536-well plates and 2 mL reactions are prepared from addition of HIS-TGFβR1 T204D or HIS-TGFβR2 WT, anti-HIS detection antibody, a labeled small molecule probe (Kd=<100 nM; koff=<0.001 s−1.) and test compounds in assay buffer (20 mM HEPES pH 7.4, 10 mM MgCl2, 0.015% Brij35, 4 mM DTT, and 0.05 mg/ml BSA). The reaction is incubated for 1 hour at room temperature and the HTRF signal was measured on an Envision plate reader (Ex: 340 nm; Em: 520 nm/495 nm). Inhibition data were calculated by comparison to no enzyme control reactions for 100% inhibition and vehicle-only reactions for 0% inhibition. The final concentration of reagents in the assay are 1 nM HIS-TGFβR1 T204D or HIS-TGFβR2 WT, 0.2 nM anti-HIS detection antibody, labeled small molecule prode (at Kd) and 0.5% DMSO. Dose response curves were generated to determine the concentration required inhibiting 50% of kinase activity (IC50). Compounds were dissolved at 10 mM in dimethylsulfoxide (DMSO) and evaluated at eleven concentrations. IC50 values were derived by non-linear regression analysis.
108
Total Activities
36
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

TGF-beta receptor type-1 (CHEMBL4439)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

TGF beta receptor antagonists
(2019)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 36 8.03 9.02
kon 36 - -
k_off 36 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5917042 3 9.02
CHEMBL5848647 3 8.96
CHEMBL5936907 3 8.96
CHEMBL5891940 3 8.92
CHEMBL5990942 3 8.89
CHEMBL5744931 3 8.89
CHEMBL5939966 3 8.85
CHEMBL5946470 3 8.85
CHEMBL5806375 3 8.82
CHEMBL5829819 3 8.74
CHEMBL5990836 3 8.66
CHEMBL5746621 3 8.54
CHEMBL6064550 3 8.42
CHEMBL5978987 3 8.38
CHEMBL5903202 3 8.36
CHEMBL5970732 3 8.33
CHEMBL5904787 3 8.33
CHEMBL5910222 3 8.29
CHEMBL6019441 3 8.29
CHEMBL5904333 3 8.24
CHEMBL5996376 3 8.21
CHEMBL6021526 3 8.19
CHEMBL5836319 3 8.18
CHEMBL5896153 3 8.00
CHEMBL5787492 3 7.92
CHEMBL5937604 3 7.75
CHEMBL6011945 3 7.70
CHEMBL5861560 3 7.62
CHEMBL4205979 3 7.54
CHEMBL5791705 3 7.48

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5917042 IC50 = 0.96 nM 9.02
CHEMBL5936907 IC50 = 1.1 nM 8.96
CHEMBL5848647 IC50 = 1.1 nM 8.96
CHEMBL5891940 IC50 = 1.2 nM 8.92
CHEMBL5990942 IC50 = 1.3 nM 8.89
CHEMBL5744931 IC50 = 1.3 nM 8.89
CHEMBL5946470 IC50 = 1.4 nM 8.85
CHEMBL5939966 IC50 = 1.4 nM 8.85
CHEMBL5806375 IC50 = 1.5 nM 8.82
CHEMBL5829819 IC50 = 1.8 nM 8.74
CHEMBL5990836 IC50 = 2.2 nM 8.66
CHEMBL5746621 IC50 = 2.9 nM 8.54
CHEMBL6064550 IC50 = 3.8 nM 8.42
CHEMBL5978987 IC50 = 4.2 nM 8.38
CHEMBL5903202 IC50 = 4.4 nM 8.36
CHEMBL5970732 IC50 = 4.7 nM 8.33
CHEMBL5904787 IC50 = 4.7 nM 8.33
CHEMBL6019441 IC50 = 5.1 nM 8.29
CHEMBL5910222 IC50 = 5.1 nM 8.29
CHEMBL5904333 IC50 = 5.8 nM 8.24
CHEMBL5996376 IC50 = 6.2 nM 8.21
CHEMBL6021526 IC50 = 6.4 nM 8.19
CHEMBL5836319 IC50 = 6.6 nM 8.18
CHEMBL5896153 IC50 = 10.0 nM 8.00
CHEMBL5787492 IC50 = 12.0 nM 7.92
CHEMBL5937604 IC50 = 18.0 nM 7.75
CHEMBL6011945 IC50 = 20.0 nM 7.70
CHEMBL5861560 IC50 = 24.0 nM 7.62
CHEMBL4205979 IC50 = 29.0 nM 7.54
CHEMBL5791705 IC50 = 33.0 nM 7.48
CHEMBL5991203 IC50 = 67.0 nM 7.17
CHEMBL5948114 IC50 = 240.0 nM 6.62
CHEMBL5903731 IC50 = 280.0 nM 6.55
CHEMBL5889396 IC50 = 310.0 nM 6.51
CHEMBL5754524 IC50 = 940.0 nM 6.03
CHEMBL5931204 IC50 = 13000.0 nM 4.89
CHEMBL5787492 kon = - -
CHEMBL5861560 kon = - -
CHEMBL5861560 k_off = - s-1 -
CHEMBL5996376 k_off = - s-1 -
CHEMBL5891940 k_off = - s-1 -
CHEMBL5891940 kon = - -
CHEMBL5791705 k_off = - s-1 -
CHEMBL5791705 kon = - -
CHEMBL5896153 k_off = - s-1 -
CHEMBL5896153 kon = - -
CHEMBL5990942 k_off = - s-1 -
CHEMBL5990942 kon = - -
CHEMBL5806375 k_off = - s-1 -
CHEMBL5904333 k_off = - s-1 -