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

CHEMBL5377322

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

Binding
Inhibition of Fam-labeled BimBH3 peptide binding to wild type N-terminal 6His-tagged human recombinant HSP70 NBD (1 to 383 residues) expressed in Escherichia coli BL21 (DE3) assessed as dissociation constant incubated for 24 hrs by fluorescence polarization assay
1
Total Activities
1
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

Exploiting the "Hot-Spots" of Hsp70<b>-</b>Bim Protein<b>-</b>Protein Interaction to Optimize the 1-Oxo-1<i>H</i>-phenalene-2,3-dicarbonitrile Analogues as Specific Hsp70<b>-</b>Bim Inhibitors.
Wang Z, Zhang H, Li X, Song Y, Wang Y, Hu Z, Gao Q, Jiang M, Yin F, Yuan L, Liu J, Song T, Lu S, Xu G, Zhang Z.
J Med Chem (2023) 66 : 16377 -16387
PubMed 38011535 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Kd 1 6.68 6.68

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5397919 1 6.68

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5397919 Kd = 210.0 nM 6.68