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Assay Detail

CHEMBL5734775

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

Binding
luminescent kinase assay: Inhibition of TgCDPK1 and CpCDPK1 was determined using a luminescent kinase assay which measures ATP depletion in the presence of the Syntide 2 peptide substrate (KinaseGlo). (U.S. Provisional Patent Application No. 61/299,286, and reference 9) Similar to TgCDPK1, exogenous calcium was necessary for CpCDPK1 to possess maximum catalytic activity (data not shown). Notably, both kinases were tested at the same ATP concentration which allows direct comparison of inhibitor potencies due to these enzymes possessing similar Kms for this cofactor. (20)Encouraged by the similar potency of inhibitor 3 against TgCDPK1 (IC50=150±20 nM) and CpCDPK1 (IC50=130±40 nM), pyrazolopyrimidine analogues that contain a naphthylmethylene group at the 3-position and various alkyl substituents at the 1-position were tested for their ability to inhibit both kinases.
225
Total Activities
75
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Tyrosine-protein kinase ABL1 (CHEMBL1862)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Compositions and methods for treating toxoplasmosis, cryptosporidiosis, and other apicomplexan protozoan related diseases
(2020)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 75 6.03 8.00
kon 75 - -
k_off 75 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2059165 3 8.00
CHEMBL5784931 3 7.48
CHEMBL1785012 3 7.16
CHEMBL1241489 3 7.12
CHEMBL5746276 3 7.06
CHEMBL1784972 3 7.05
CHEMBL170250 3 7.03
CHEMBL406845 3 6.76
CHEMBL5860627 3 6.71
CHEMBL1785014 3 6.70
CHEMBL1242384 3 6.62
CHEMBL2030556 3 6.52
CHEMBL2078865 3 6.50
CHEMBL2079136 3 6.45
CHEMBL1784969 3 6.44
CHEMBL5774425 3 6.39
CHEMBL2079317 3 6.30
CHEMBL2059166 3 6.26
CHEMBL2078794 3 6.20
CHEMBL5896441 3 6.19
CHEMBL2079167 3 6.17
CHEMBL1785020 3 6.09
CHEMBL2079214 3 6.08
CHEMBL5932426 3 6.01
CHEMBL5918917 3 5.97
CHEMBL2079215 3 5.94
CHEMBL5767089 3 5.91
CHEMBL5875647 3 5.90
CHEMBL2079137 3 5.80
CHEMBL2078815 3 5.79

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2059165 IC50 = 10.0 nM 8.00
CHEMBL5784931 IC50 = 33.3 nM 7.48
CHEMBL1785012 IC50 = 70.0 nM 7.16
CHEMBL1241489 IC50 = 75.0 nM 7.12
CHEMBL5746276 IC50 = 86.2 nM 7.06
CHEMBL1784972 IC50 = 90.0 nM 7.05
CHEMBL170250 IC50 = 94.0 nM 7.03
CHEMBL406845 IC50 = 172.0 nM 6.76
CHEMBL5860627 IC50 = 194.0 nM 6.71
CHEMBL1785014 IC50 = 200.0 nM 6.70
CHEMBL1242384 IC50 = 238.0 nM 6.62
CHEMBL2030556 IC50 = 304.0 nM 6.52
CHEMBL2078865 IC50 = 316.0 nM 6.50
CHEMBL2079136 IC50 = 353.0 nM 6.45
CHEMBL1784969 IC50 = 360.0 nM 6.44
CHEMBL5774425 IC50 = 403.0 nM 6.39
CHEMBL2079317 IC50 = 497.0 nM 6.30
CHEMBL2059166 IC50 = 554.0 nM 6.26
CHEMBL2078794 IC50 = 636.0 nM 6.20
CHEMBL5896441 IC50 = 649.0 nM 6.19
CHEMBL2079167 IC50 = 675.0 nM 6.17
CHEMBL1785020 IC50 = 820.0 nM 6.09
CHEMBL2079214 IC50 = 838.0 nM 6.08
CHEMBL5932426 IC50 = 969.0 nM 6.01
CHEMBL5918917 IC50 = 1073.0 nM 5.97
CHEMBL2079215 IC50 = 1153.0 nM 5.94
CHEMBL5767089 IC50 = 1230.0 nM 5.91
CHEMBL5875647 IC50 = 1267.0 nM 5.90
CHEMBL2079137 IC50 = 1589.0 nM 5.80
CHEMBL2078815 IC50 = 1636.0 nM 5.79
CHEMBL2079232 IC50 = 1680.0 nM 5.78
CHEMBL5983391 IC50 = 1701.0 nM 5.77
CHEMBL1242754 IC50 = 1700.0 nM 5.77
CHEMBL1785021 IC50 = 1700.0 nM 5.77
CHEMBL5776934 IC50 = 1798.0 nM 5.75
CHEMBL5889864 IC50 = 2010.0 nM 5.70
CHEMBL2079138 IC50 = 2360.0 nM 5.63
CHEMBL2079213 IC50 = 2943.0 nM 5.53
CHEMBL5861083 IC50 = 4159.0 nM 5.38
CHEMBL5814019 IC50 = 4790.0 nM 5.32
CHEMBL2079229 IC50 = 4861.0 nM 5.31
CHEMBL2030558 IC50 = 5982.0 nM 5.22
CHEMBL1231371 IC50 = 6000.0 nM 5.22
CHEMBL5909447 IC50 = 6350.0 nM 5.20
CHEMBL2078805 IC50 = 7340.0 nM 5.13
CHEMBL6047364 IC50 = 7326.0 nM 5.13
CHEMBL5785484 IC50 = 7845.0 nM 5.11
CHEMBL573578 IC50 = 7700.0 nM 5.11
CHEMBL1231370 IC50 = 7900.0 nM 5.10
CHEMBL2078771 IC50 = 8040.0 nM 5.09