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Assay Detail

CHEMBL2072022

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

Binding
Inhibition of human KIAA1363 expressed in 293T/17 cells using 2-thioacetyl MAGE as substrate after 1 hr by serine hydrolase activity-based probe assay
1
Total Activities
1
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

Neutral cholesterol ester hydrolase 1 (CHEMBL5048)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and structure-activity relationship of (1-halo-2-naphthyl) carbamate-based inhibitors of KIAA1363 (NCEH1/AADACL1).
Shreder KR, Lin EC, Wu J, Cajica J, Amantea CM, Hu Y, Okerberg E, Brown HE, Pham LM, Chung de M, Fraser AS, McGee E, Rosenblum JS, Kozarich JW.
Bioorg Med Chem Lett (2012) 22 : 5748 -5751
PubMed 22877630 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 6.82 6.82

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2069333 1 6.82

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2069333 IC50 = 150.0 nM 6.82