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Assay Detail

CHEMBL5731200

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Binding
Inhibitory Activity Against IDH1R132H and IDH1R132C Enzymes: The IDH1R132H protein and the IDH1R132C protein were prepared as follows: the IDH1R132H or IDH1R132C gene was integrated into a pET24b(+) vector (Novagen) to prepare a construct for C-terminal fusion of 6× histidine tag. After transformation of Rosetta 2 (DE3) E. coli, the expression of the protein was induced with IPTG. The E. coli was collected and homogenized, followed by the affinity purification of the 6× histidine fusion protein using HisTrap HP columns (GE Healthcare Japan Corp.) and gel filtration purification using Superdex 200 columns (GE Healthcare Japan Corp.) to obtain the IDH1R132H or IDH1R132C protein of interest.IDH1R132H and IDH1R132C each convert 2-oxoglutarate and NADPH to D-2-hydroxyglutarate (2-HG) and NADP+. Therefore, the activity of the IDH1R132H and IDH1R132C enzymes can be measured by detecting NADPH levels.The enzyme inhibitory activity evaluation was carried out as follows: 40 μL each of reaction solutions containing different concentrations of each compound (100 mM Tris-HCl (pH 7.5), 150 mM NaCl, 20 mM MgCl2, 0.5 mg/mL bovine serum albumin, 1 mM reduced glutathione, 40 μM NADPH, 0.5 mM 2-oxoglutarate, 0.5% dimethyl sulfoxide, 50000 to 0.128 nM compound, and 12 nM IDH1R132H or 10 nM IDH1R132C as the enzyme) was added to each well of 384-well plates (Greiner Bio One International GmbH, #781096) and incubated at room temperature. While NADPH-derived fluorescence was occasionally monitored, the reaction was terminated by the addition of 5 μL of 0.5 M EDTA before consumption of NADPH. 5 μL of WST-8 reagent (Dojindo Laboratories, #CK04) was further added and mixed therewith. 15 minutes later, the absorbance at 450 nm was measured using a plate reader (PerkinElmer, Inc., EnVision). The observed absorbance value reflects the amount of residual NADPH. From the absorbance data, the enzyme inhibitory activity of each compound at each concentration was calculated and analyzed using medical statistical analysis software GraphPad Prism to calculate an IC50 value.
501
Total Activities
165
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

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

Target

Isocitrate dehydrogenase [NADP] cytoplasmic (CHEMBL2007625)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Isoxazole derivative as mutant isocitrate dehydrogenase 1 inhibitor
(2018)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 167 6.83 7.33
kon 167 - -
k_off 167 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL6010394 3 7.33
CHEMBL5879831 3 7.26
CHEMBL5851342 3 7.25
CHEMBL6008217 3 7.25
CHEMBL5633305 3 7.24
CHEMBL5865972 3 7.23
CHEMBL5803473 3 7.21
CHEMBL5821606 3 7.19
CHEMBL5765619 3 7.17
CHEMBL5633056 3 7.12
CHEMBL5805970 3 7.11
CHEMBL5965058 3 7.10
CHEMBL6051292 3 7.10
CHEMBL6050241 3 7.10
CHEMBL5963792 3 7.10
CHEMBL6007687 3 7.09
CHEMBL6006233 3 7.09
CHEMBL5758031 3 7.09
CHEMBL6037555 3 7.08
CHEMBL5933529 3 7.07
CHEMBL5871602 3 7.06
CHEMBL5825278 3 7.06
CHEMBL5936332 3 7.05
CHEMBL5840478 3 7.04
CHEMBL5824394 3 7.03
CHEMBL5831173 3 7.03
CHEMBL5945875 3 7.03
CHEMBL5977748 3 7.03
CHEMBL5967524 3 7.03
CHEMBL4651002 SAFUSIDENIB 2.0 6 7.02

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL6010394 IC50 = 47.0 nM 7.33
CHEMBL5879831 IC50 = 55.0 nM 7.26
CHEMBL6008217 IC50 = 56.0 nM 7.25
CHEMBL5851342 IC50 = 56.0 nM 7.25
CHEMBL5633305 IC50 = 57.0 nM 7.24
CHEMBL5865972 IC50 = 59.0 nM 7.23
CHEMBL5803473 IC50 = 62.0 nM 7.21
CHEMBL5821606 IC50 = 64.0 nM 7.19
CHEMBL5765619 IC50 = 67.0 nM 7.17
CHEMBL5633056 IC50 = 75.0 nM 7.12
CHEMBL5805970 IC50 = 78.0 nM 7.11
CHEMBL6051292 IC50 = 80.0 nM 7.10
CHEMBL6050241 IC50 = 79.0 nM 7.10
CHEMBL5963792 IC50 = 80.0 nM 7.10
CHEMBL5965058 IC50 = 79.0 nM 7.10
CHEMBL6006233 IC50 = 81.0 nM 7.09
CHEMBL6007687 IC50 = 81.0 nM 7.09
CHEMBL5758031 IC50 = 81.0 nM 7.09
CHEMBL6037555 IC50 = 84.0 nM 7.08
CHEMBL5933529 IC50 = 85.0 nM 7.07
CHEMBL5825278 IC50 = 88.0 nM 7.06
CHEMBL5871602 IC50 = 87.0 nM 7.06
CHEMBL5936332 IC50 = 90.0 nM 7.05
CHEMBL5840478 IC50 = 91.0 nM 7.04
CHEMBL5824394 IC50 = 94.0 nM 7.03
CHEMBL5967524 IC50 = 93.0 nM 7.03
CHEMBL5977748 IC50 = 94.0 nM 7.03
CHEMBL5831173 IC50 = 94.0 nM 7.03
CHEMBL5945875 IC50 = 93.0 nM 7.03
CHEMBL4651002 SAFUSIDENIB IC50 = 95.0 nM 7.02
CHEMBL5935058 IC50 = 95.0 nM 7.02
CHEMBL6035971 IC50 = 96.0 nM 7.02
CHEMBL5742487 IC50 = 95.0 nM 7.02
CHEMBL6047413 IC50 = 98.0 nM 7.01
CHEMBL5971353 IC50 = 98.0 nM 7.01
CHEMBL5981049 IC50 = 98.0 nM 7.01
CHEMBL5870059 IC50 = 98.0 nM 7.01
CHEMBL5897935 IC50 = 98.0 nM 7.01
CHEMBL5826039 IC50 = 99.0 nM 7.00
CHEMBL5895300 IC50 = 102.0 nM 6.99
CHEMBL6050854 IC50 = 104.0 nM 6.98
CHEMBL6005942 IC50 = 104.0 nM 6.98
CHEMBL5982851 IC50 = 107.0 nM 6.97
CHEMBL5838997 IC50 = 107.0 nM 6.97
CHEMBL5831408 IC50 = 107.0 nM 6.97
CHEMBL5811289 IC50 = 106.0 nM 6.97
CHEMBL5984778 IC50 = 109.0 nM 6.96
CHEMBL5913603 IC50 = 110.0 nM 6.96
CHEMBL5930301 IC50 = 110.0 nM 6.96
CHEMBL5872310 IC50 = 109.0 nM 6.96