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Assay Detail

CHEMBL3707962

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Binding
Biological Assay: Endothelial lipase (EL) and hepatic lipase (HL) activities were measured using a fluorescent substrate, A10070, (Invitrogen, CA) doped into an artificial vesicle containing DMPG (Avanti Polar Lipids) as the excipient. Vesicles were prepared by combining 571 uL of 29 mM DMPG in a 1:1 mixture of MeOH and CHCl3 with 2000 uL of 1 mM A10070 in a 1:1 mixture of MeOH and CHCl3. The mixture was dried under nitrogen in multiple vials then resuspended in 20 mL total volume of 50 mM HEPES pH 8.0 buffer containing 50 mM NaCl and 0.2 mM EDTA. The sample was allowed to sit at room temperature for 15 min and then was sonicated 3x4 mins on ice with a Branson Sonicator using duty cycle 1. This preparation provides vesicles with a mole fraction of 0.11 for the FRET substrate.The enzymatic assay was measured using 384-well white Optiplates. Each well contained 20 uL of assay buffer (50 mM HEPES pH 8.0, 50 mM NaCl and 1 mM CaCl2) and 0.25 uL of a DMSO solution containing a compound.
345
Total Activities
340
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Hepatic triacylglycerol lipase (CHEMBL2127)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Amide, urea or sulfone amide linked benzothiazole inhibitors of endothelial lipase
(2015)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 345 7.00 9.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3677564 1 9.30
CHEMBL3677604 1 9.10
CHEMBL3677538 1 9.10
CHEMBL3677562 1 9.10
CHEMBL3677630 1 9.00
CHEMBL3672652 1 9.00
CHEMBL3677580 1 8.85
CHEMBL3677632 1 8.82
CHEMBL3672654 1 8.72
CHEMBL3677540 1 8.72
CHEMBL3682478 1 8.68
CHEMBL3677434 1 8.66
CHEMBL3677571 1 8.62
CHEMBL3677433 1 8.59
CHEMBL3672653 1 8.59
CHEMBL3677610 1 8.59
CHEMBL3677607 1 8.55
CHEMBL3677537 1 8.55
CHEMBL3677550 1 8.55
CHEMBL3677608 1 8.54
CHEMBL3677543 1 8.52
CHEMBL3677601 1 8.52
CHEMBL3677563 1 8.44
CHEMBL3677545 1 8.44
CHEMBL3677547 1 8.44
CHEMBL3677602 1 8.29
CHEMBL3677548 1 8.28
CHEMBL3682490 1 8.17
CHEMBL3677439 1 8.15
CHEMBL3677567 1 8.14

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3677564 IC50 = 0.5 nM 9.30
CHEMBL3677604 IC50 = 0.8 nM 9.10
CHEMBL3677538 IC50 = 0.8 nM 9.10
CHEMBL3677562 IC50 = 0.8 nM 9.10
CHEMBL3677630 IC50 = 1.0 nM 9.00
CHEMBL3672652 IC50 = 1.0 nM 9.00
CHEMBL3677580 IC50 = 1.4 nM 8.85
CHEMBL3677632 IC50 = 1.5 nM 8.82
CHEMBL3677540 IC50 = 1.9 nM 8.72
CHEMBL3672654 IC50 = 1.9 nM 8.72
CHEMBL3682478 IC50 = 2.1 nM 8.68
CHEMBL3677434 IC50 = 2.2 nM 8.66
CHEMBL3677571 IC50 = 2.4 nM 8.62
CHEMBL3677433 IC50 = 2.6 nM 8.59
CHEMBL3677610 IC50 = 2.6 nM 8.59
CHEMBL3672653 IC50 = 2.6 nM 8.59
CHEMBL3677607 IC50 = 2.8 nM 8.55
CHEMBL3677550 IC50 = 2.8 nM 8.55
CHEMBL3677537 IC50 = 2.8 nM 8.55
CHEMBL3677608 IC50 = 2.9 nM 8.54
CHEMBL3677543 IC50 = 3.0 nM 8.52
CHEMBL3677601 IC50 = 3.0 nM 8.52
CHEMBL3677547 IC50 = 3.6 nM 8.44
CHEMBL3677563 IC50 = 3.6 nM 8.44
CHEMBL3677545 IC50 = 3.6 nM 8.44
CHEMBL3677602 IC50 = 5.1 nM 8.29
CHEMBL3677548 IC50 = 5.2 nM 8.28
CHEMBL3682490 IC50 = 6.7 nM 8.17
CHEMBL3677439 IC50 = 7.1 nM 8.15
CHEMBL3677567 IC50 = 7.3 nM 8.14
CHEMBL3677553 IC50 = 7.7 nM 8.11
CHEMBL3677581 IC50 = 9.4 nM 8.03
CHEMBL3677554 IC50 = 10.0 nM 8.00
CHEMBL3677462 IC50 = 10.0 nM 8.00
CHEMBL3672632 IC50 = 10.0 nM 8.00
CHEMBL3677465 IC50 = 11.0 nM 7.96
CHEMBL3677480 IC50 = 11.0 nM 7.96
CHEMBL3677498 IC50 = 11.0 nM 7.96
CHEMBL3672638 IC50 = 11.0 nM 7.96
CHEMBL3677463 IC50 = 11.0 nM 7.96
CHEMBL3677572 IC50 = 12.0 nM 7.92
CHEMBL3677475 IC50 = 12.0 nM 7.92
CHEMBL3677474 IC50 = 13.0 nM 7.89
CHEMBL3677492 IC50 = 13.0 nM 7.89
CHEMBL3682495 IC50 = 13.0 nM 7.89
CHEMBL3677525 IC50 = 13.0 nM 7.89
CHEMBL3682466 IC50 = 13.7 nM 7.86
CHEMBL3677539 IC50 = 13.9 nM 7.86
CHEMBL3672640 IC50 = 14.0 nM 7.85
CHEMBL3682498 IC50 = 14.3 nM 7.84