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BioAssay: AID 266546

Inhibition of BODIPY-AG binding to human HSP90

17-Allylamino-17-demethoxygeldanamycin (17-AAG)1 is a semisynthetic inhibitor of the 90 kDa heat shock protein (Hsp90) currently in clinical trials for the treatment of cancer. However, 17-AAG faces challenging formulation issues due to its poor solubility. Here we report the synthesis and evaluation of a highly soluble hydroquinone hydrochloride derivative of 17-AAG, 1a (IPI-504), and several of more ..
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 Tested Compounds
 Tested Compounds
All(12)
 
 
Active(9)
 
 
Unspecified(3)
 
 
 Tested Substances
 Tested Substances
All(12)
 
 
Active(9)
 
 
Unspecified(3)
 
 
AID: 266546
Data Source: ChEMBL (365491)
BioAssay Type: Confirmatory, Concentration-Response Relationship Observed
Depositor Category: Literature, Extracted
BioAssay Version:
Deposit Date: 2010-05-24
Modify Date: 2014-08-25

Data Table ( Complete ):           View Active Data    View All Data
Targets
Sequence: RecName: Full=Heat shock protein HSP 90-beta; Short=HSP 90; AltName: Full=Heat shock 84 kDa; Short=HSP 84; Short=HSP84
Description ..   
Protein Family: Hsp90 protein
Comment ..   

Gene:HSP90AB1     Related Protein 3D Structures     More BioActivity Data..


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BioActive Compounds: 9
Description:
Title: Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90.

Abstract: 17-Allylamino-17-demethoxygeldanamycin (17-AAG)1 is a semisynthetic inhibitor of the 90 kDa heat shock protein (Hsp90) currently in clinical trials for the treatment of cancer. However, 17-AAG faces challenging formulation issues due to its poor solubility. Here we report the synthesis and evaluation of a highly soluble hydroquinone hydrochloride derivative of 17-AAG, 1a (IPI-504), and several of the physiological metabolites. These compounds show comparable binding affinity to human Hsp90 and its endoplasmic reticulum (ER) homologue, the 94 kDa glucose regulated protein (Grp94). Furthermore, the compounds inhibit the growth of the human cancer cell lines SKBR3 and SKOV3, which overexpress Hsp90 client protein Her2, and cause down-regulation of Her2 as well as induction of Hsp70 consistent with Hsp90 inhibition. There is a clear correlation between the measured binding affinity of the compounds and their cellular activities. Upon the basis of its potent activity against Hsp90 and a significant improvement in solubility, 1a is currently under evaluation in Phase I clinical trials for cancer.
(PMID: 16854066)
Comment
Compounds with activity <= 50uM or explicitly reported as active by ChEMBL are flagged as active in this PubChem assay presentation.
Categorized Comment - additional comments and annotations
From BioAssay Depositor:
Assay Type: Binding
Target Type: Target is a group of closely related proteins
Assay Data Source: Scientific Literature
Result Definitions
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TIDNameDescriptionHistogramTypeUnit
OutcomeThe BioAssay activity outcomeOutcome
1EC50*EC50 PubChem standard valueFloatμM
3BEIBinding Efficiency Index(nM)Float
2SEISurface Efficiency Index(nM)Float
4LELigand EfficiencyFloat
5LLELipophilic Ligand EfficiencyFloat
6EC50 activity commentEC50 activity commentString
7EC50 standard flagEC50 standard flagInteger
8EC50 qualifierEC50 qualifierString
9EC50 published valueEC50 published valueFloatmM
10EC50 standard valueEC50 standard valueFloatnM
11EC50 data validityEC50 data validityString
12EC50 activity commentEC50 activity commentString
13EC50 standard flagEC50 standard flagInteger
14EC50 qualifierEC50 qualifierString
15EC50 published valueEC50 published valueFloatnM
16EC50 standard valueEC50 standard valueFloatnM
17EC50 data validityEC50 data validityString
18EC50 activity commentEC50 activity commentString
19EC50 standard flagEC50 standard flagInteger
20EC50 qualifierEC50 qualifierString
21EC50 published valueEC50 published valueFloatμM
22EC50 standard valueEC50 standard valueFloatnM
23EC50 data validityEC50 data validityString

* Activity Concentration.

Data Table (Concise)
Data Table ( Complete ):     View Active Data    View All Data
Classification
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