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Assay Detail

CHEMBL709173

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

Binding
Inhibition of human MMP-3.
13
Total Activities
13
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

Stromelysin-1 (CHEMBL283)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design, synthesis, and structure-activity relationships of macrocyclic hydroxamic acids that inhibit tumor necrosis factor alpha release in vitro and in vivo.
Xue CB, Voss ME, Nelson DJ, Duan JJ, Cherney RJ, Jacobson IC, He X, Roderick J, Chen L, Corbett RL, Wang L, Meyer DT, Kennedy K, DeGradodagger WF, Hardman KD, Teleha CA, Jaffee BD, Liu RQ, Copeland RA, Covington MB, Christ DD, Trzaskos JM, Newton RC, Magolda RL, Wexler RR, Decicco CP.
J Med Chem (2001) 44 : 2636 -2660
PubMed 11472217 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 13 8.09 8.71

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL417537 1 8.71
CHEMBL279785 MARIMASTAT 3.0 1 8.62
CHEMBL88718 1 8.54
CHEMBL92385 1 8.52
CHEMBL23725 1 8.52
CHEMBL24761 1 8.47
CHEMBL91636 1 8.11
CHEMBL88520 1 7.85
CHEMBL328090 1 7.79
CHEMBL329124 1 7.65
CHEMBL48258 1 7.62
CHEMBL45631 1 7.49
CHEMBL433381 1 7.32

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL417537 Ki = 1.93 nM 8.71
CHEMBL279785 MARIMASTAT Ki = 2.4 nM 8.62
CHEMBL88718 Ki = 2.88 nM 8.54
CHEMBL92385 Ki = 3.0 nM 8.52
CHEMBL23725 Ki = 3.0 nM 8.52
CHEMBL24761 Ki = 3.4 nM 8.47
CHEMBL91636 Ki = 7.8 nM 8.11
CHEMBL88520 Ki = 14.0 nM 7.85
CHEMBL328090 Ki = 16.2 nM 7.79
CHEMBL329124 Ki = 22.3 nM 7.65
CHEMBL48258 Ki = 24.1 nM 7.62
CHEMBL45631 Ki = 32.7 nM 7.49
CHEMBL433381 Ki = 48.0 nM 7.32