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Assay Detail

CHEMBL5232437

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

Binding
Inhibition of B-Raf V600E mutant (448 to 723 residues) (unknown origin) expressed in Escherichia coli by AlphaScreen 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

Serine/threonine-protein kinase B-raf (CHEMBL5145)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

From Hit Seeking to Magic Bullets: The Successful Union of Epigenetic and Fragment Based Drug Discovery (EPIDD + FBDD).
Vaidergorn MM, da Silva Emery F, Ganesan A.
J Med Chem (2021) 64 : 13980 -14010
PubMed 34591474 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 7.89 7.89

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1229517 VEMURAFENIB 4.0 1 7.89

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1229517 VEMURAFENIB IC50 = 13.0 nM 7.89