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

CHEMBL718404

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

Binding
Inhibition of matrix metalloprotease-16
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Matrix metalloproteinase-16 (CHEMBL2200)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of macrocyclic hydroxamic acids containing biphenylmethyl derivatives at P1', a series of selective TNF-alpha converting enzyme inhibitors with potent cellular activity in the inhibition of TNF-alpha release.
Xue CB, He X, Corbett RL, Roderick J, Wasserman ZR, Liu RQ, Jaffee BD, Covington MB, Qian M, Trzaskos JM, Newton RC, Magolda RL, Wexler RR, Decicco CP.
J Med Chem (2001) 44 : 3351 -3354
PubMed 11585440 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 4 5.70 5.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL325163 1 5.70
CHEMBL431680 1 -
CHEMBL115263 1 -
CHEMBL114878 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL325163 Ki = 2000.0 nM 5.70
CHEMBL431680 Ki > 2000.0 nM -
CHEMBL115263 Ki > 2000.0 nM -
CHEMBL114878 Ki > 2000.0 nM -