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

CHEMBL5331955

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

Binding
Inhibition of wild type N-terminal 6His-tagged BRAF V600E mutant (unknown origin) (D448 to K723 residues) expressed in baculovirus expression system 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

A decade of approved first-in-class small molecule orphan drugs: Achievements, challenges and perspectives.
Gu J, Wu Q, Zhang Q, You Q, Wang L.
Eur J Med Chem (2022) 243 : 114742 -114742
PubMed 36155354 · 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