Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL5579508

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

Toxicity
Inhibition of recombinant human full-length ADAMTS5 using FAM-Thr-Glu-Ser-Glu-Ser-Arg-Gly-Ala-Ile-Tyr-Lys-Lys-TAMRA as substrate by FRET assay
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Publication

Design, synthesis and biological evaluation of arylsulfonamides as ADAMTS7 inhibitors.
Cuffaro D, Burkhard T, Bernardoni BL, Di Leo R, Zhang X, Galati S, Tuccinardi T, Macchia M, Rossello A, Santamaria S, de Groot R, Nuti E.
RSC Med Chem (2024) 15 : 2806 -2825
PubMed 39149096 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 12 7.12 8.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5595366 1 8.52
CHEMBL5589746 1 8.52
CHEMBL5591230 1 8.22
CHEMBL5594088 1 8.05
CHEMBL5593176 1 8.00
CHEMBL5592306 1 7.82
CHEMBL5593273 1 7.05
CHEMBL5594880 1 7.05
CHEMBL5589804 1 6.96
CHEMBL5593591 1 5.42
CHEMBL5590061 1 4.96
CHEMBL5592123 1 4.89

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5595366 Ki = 3.0 nM 8.52
CHEMBL5589746 Ki = 3.0 nM 8.52
CHEMBL5591230 Ki = 6.0 nM 8.22
CHEMBL5594088 Ki = 9.0 nM 8.05
CHEMBL5593176 Ki = 10.0 nM 8.00
CHEMBL5592306 Ki = 15.0 nM 7.82
CHEMBL5593273 Ki = 90.0 nM 7.05
CHEMBL5594880 Ki = 90.0 nM 7.05
CHEMBL5589804 Ki = 110.0 nM 6.96
CHEMBL5593591 Ki = 3800.0 nM 5.42
CHEMBL5590061 Ki = 11000.0 nM 4.96
CHEMBL5592123 Ki = 13000.0 nM 4.89