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

CHEMBL867907

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

Binding
Inhibition of BODIPY-AG binding to human HSP90
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 5 — Multiple protein complex / RNA
Curated By Autocuration

Target

Heat shock protein HSP90 (CHEMBL2095165)
Type PROTEIN FAMILY
Organism Homo sapiens

Publication

Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90.
Ge J, Normant E, Porter JR, Ali JA, Dembski MS, Gao Y, Georges AT, Grenier L, Pak RH, Patterson J, Sydor JR, Tibbitts TT, Tong JK, Adams J, Palombella VJ.
J Med Chem (2006) 49 : 4606 -4615
PubMed 16854066 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 12 6.70 7.47

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL339231 1 7.47
CHEMBL209356 1 7.47
CHEMBL383824 ALVESPIMYCIN 2.0 1 7.21
CHEMBL377559 RETASPIMYCIN HYDROCHLORIDE 3.0 1 7.20
CHEMBL211296 1 7.18
CHEMBL211295 1 7.04
CHEMBL109480 TANESPIMYCIN 3.0 1 6.92
CHEMBL378936 1 6.27
CHEMBL378935 1 6.22
CHEMBL14830 ADENOSINE DIPHOSPHATE 0.5 1 4.06
CHEMBL14249 ADENOSINE TRIPHOSPHATE 2.0 1 -
CHEMBL377782 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL339231 EC50 = 34.0 nM 7.47
CHEMBL209356 EC50 = 34.0 nM 7.47
CHEMBL383824 ALVESPIMYCIN EC50 = 62.0 nM 7.21
CHEMBL377559 RETASPIMYCIN HYDROCHLORIDE EC50 = 63.0 nM 7.20
CHEMBL211296 EC50 = 66.0 nM 7.18
CHEMBL211295 EC50 = 91.0 nM 7.04
CHEMBL109480 TANESPIMYCIN EC50 = 119.0 nM 6.92
CHEMBL378936 EC50 = 541.0 nM 6.27
CHEMBL378935 EC50 = 603.0 nM 6.22
CHEMBL14830 ADENOSINE DIPHOSPHATE EC50 = 87000.0 nM 4.06
CHEMBL14249 ADENOSINE TRIPHOSPHATE EC50 = 1500000.0 nM -
CHEMBL377782 EC50 > 10000.0 nM -