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Assay Detail

CHEMBL3705746

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Binding
In Vitro Inhibition Assay: An in vitro assay showed inhibition of CXCR2-mediated intracellular calcium release. Briefly, human neutrophils were suspended in HBSS- (without Ca2+ and Mg2+) containing 10 mM HEPES and FLIPR Calcium 3 dye (3.1x107 cells in total volume 1.7 mL). Cells were aliquoted (200 uL of the cell suspension per tube, 8 tubes total) and 2 uL of the designated compound (with appropriate dilutions) were added to each of 6 tubes. As controls, 2 uL of DMSO (1% final concentration) were added to 2 other tubes. Cells were incubated for 30 min at 37 C. After dye loading, tubes were centrifuged at 6,000 rpm for 1 min, supernatant was removed and the cell pellet was re-suspended in 200 uL of HBSS+ (with Ca2+ and Mg2+) containing 10 mM HEPES. The test compound or DMSO (control) was added again at the same concentrations that were used during cell loading. The cell suspension was aliquoted into a 96-well Reading Plate (Corning) in a volume of 90 uL (105 cells/well).
177
Total Activities
177
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

C-X-C chemokine receptor type 2 (CHEMBL2434)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Pyrimidinecarboxamides as CXCR2 modulators
(2015)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 177 6.37 7.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3658321 1 7.85
CHEMBL3658278 1 7.80
CHEMBL3426944 1 7.66
CHEMBL3654441 1 7.55
CHEMBL3658341 1 7.50
CHEMBL3658338 1 7.43
CHEMBL3342269 1 7.42
CHEMBL3426949 1 7.28
CHEMBL3654444 1 7.23
CHEMBL3654446 1 7.14
CHEMBL3342320 1 7.11
CHEMBL3426945 1 7.10
CHEMBL3639571 1 7.09
CHEMBL3342318 1 6.98
CHEMBL3658241 1 6.95
CHEMBL3658340 1 6.94
CHEMBL3658343 1 6.78
CHEMBL3342312 1 6.76
CHEMBL3658323 1 6.71
CHEMBL3658274 1 6.68
CHEMBL3658260 1 6.67
CHEMBL3342304 1 6.56
CHEMBL3342313 1 6.56
CHEMBL3342314 1 6.56
CHEMBL3342319 1 6.53
CHEMBL3658245 1 6.46
CHEMBL3426951 1 6.41
CHEMBL3342291 1 6.41
CHEMBL3658335 1 6.28
CHEMBL3342317 1 6.28

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3658321 IC50 = 14.0 nM 7.85
CHEMBL3658278 IC50 = 16.0 nM 7.80
CHEMBL3426944 IC50 = 22.0 nM 7.66
CHEMBL3654441 IC50 = 28.0 nM 7.55
CHEMBL3658341 IC50 = 32.0 nM 7.50
CHEMBL3658338 IC50 = 37.0 nM 7.43
CHEMBL3342269 IC50 = 38.0 nM 7.42
CHEMBL3426949 IC50 = 52.0 nM 7.28
CHEMBL3654444 IC50 = 59.0 nM 7.23
CHEMBL3654446 IC50 = 72.0 nM 7.14
CHEMBL3342320 IC50 = 78.0 nM 7.11
CHEMBL3426945 IC50 = 79.0 nM 7.10
CHEMBL3639571 IC50 = 81.0 nM 7.09
CHEMBL3342318 IC50 = 105.0 nM 6.98
CHEMBL3658241 IC50 = 112.0 nM 6.95
CHEMBL3658340 IC50 = 116.0 nM 6.94
CHEMBL3658343 IC50 = 166.0 nM 6.78
CHEMBL3342312 IC50 = 173.0 nM 6.76
CHEMBL3658323 IC50 = 194.0 nM 6.71
CHEMBL3658274 IC50 = 210.0 nM 6.68
CHEMBL3658260 IC50 = 216.0 nM 6.67
CHEMBL3342304 IC50 = 277.0 nM 6.56
CHEMBL3342313 IC50 = 275.0 nM 6.56
CHEMBL3342314 IC50 = 278.0 nM 6.56
CHEMBL3342319 IC50 = 294.0 nM 6.53
CHEMBL3658245 IC50 = 350.0 nM 6.46
CHEMBL3342291 IC50 = 393.0 nM 6.41
CHEMBL3426951 IC50 = 387.0 nM 6.41
CHEMBL3342317 IC50 = 520.0 nM 6.28
CHEMBL3658335 IC50 = 529.0 nM 6.28
CHEMBL3342282 IC50 = 542.0 nM 6.27
CHEMBL3654443 IC50 = 611.0 nM 6.21
CHEMBL3426947 IC50 = 689.0 nM 6.16
CHEMBL3658334 IC50 = 703.0 nM 6.15
CHEMBL3342310 IC50 = 759.0 nM 6.12
CHEMBL3658246 IC50 = 760.0 nM 6.12
CHEMBL3658316 IC50 = 780.0 nM 6.11
CHEMBL3658273 IC50 = 852.0 nM 6.07
CHEMBL3426952 IC50 = 899.0 nM 6.05
CHEMBL3342321 IC50 = 890.0 nM 6.05
CHEMBL3658303 IC50 = 981.0 nM 6.01
CHEMBL3654442 IC50 = 1060.0 nM 5.97
CHEMBL3658288 IC50 = 1150.0 nM 5.94
CHEMBL3658349 IC50 = 1190.0 nM 5.92
CHEMBL3342290 IC50 = 1210.0 nM 5.92
CHEMBL3654445 IC50 = 1230.0 nM 5.91
CHEMBL3658348 IC50 = 1230.0 nM 5.91
CHEMBL3658336 IC50 = 1230.0 nM 5.91
CHEMBL3658311 IC50 = 1250.0 nM 5.90
CHEMBL3342311 IC50 = 1480.0 nM 5.83