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Assay Detail

CHEMBL839587

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Binding
Inhibitory activity against mitogen-activated protein kinase p38
16
Total Activities
16
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Design and synthesis of potent pyridazine inhibitors of p38 MAP kinase.
Tamayo N, Liao L, Goldberg M, Powers D, Tudor YY, Yu V, Wong LM, Henkle B, Middleton S, Syed R, Harvey T, Jang G, Hungate R, Dominguez C.
Bioorg Med Chem Lett (2005) 15 : 2409 -2413
PubMed 15837335 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 16 7.66 8.80

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL365359 1 8.80
CHEMBL372301 1 8.74
CHEMBL265032 1 8.68
CHEMBL197041 1 8.22
CHEMBL436291 1 8.15
CHEMBL197096 1 8.14
CHEMBL195188 1 8.04
CHEMBL193992 1 7.99
CHEMBL426466 1 7.69
CHEMBL193563 1 7.53
CHEMBL363600 1 7.50
CHEMBL197267 1 7.25
CHEMBL193494 1 7.18
CHEMBL196295 1 6.75
CHEMBL193983 1 6.15
CHEMBL196847 1 5.75

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL365359 Ki = 1.6 nM 8.80
CHEMBL372301 Ki = 1.8 nM 8.74
CHEMBL265032 Ki = 2.1 nM 8.68
CHEMBL197041 Ki = 6.0 nM 8.22
CHEMBL436291 Ki = 7.0 nM 8.15
CHEMBL197096 Ki = 7.3 nM 8.14
CHEMBL195188 Ki = 9.2 nM 8.04
CHEMBL193992 Ki = 10.2 nM 7.99
CHEMBL426466 Ki = 20.4 nM 7.69
CHEMBL193563 Ki = 29.7 nM 7.53
CHEMBL363600 Ki = 31.8 nM 7.50
CHEMBL197267 Ki = 56.2 nM 7.25
CHEMBL193494 Ki = 65.9 nM 7.18
CHEMBL196295 Ki = 179.3 nM 6.75
CHEMBL193983 Ki = 709.0 nM 6.15
CHEMBL196847 Ki = 1772.0 nM 5.75