Radicicol

SKU:BHB11900008
Suppliers
StressMarq Biosciences Inc.
StressMarq Biosciences Inc.
Details Products
Overview
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Radicicol is a research-grade small-molecule inhibitor of Hsp90 for Cancer and Heat Shock studies. Supplied as a white to yellow solid with 97% purity (CAS 12772-57-5, MW 364.8) soluble in DMSO; store at -20°C. For research use only.
Cas No. 12772-57-5
Molecular Formula C18H17CIO6
Purity 97% by TLC
Application Notes Hsp90 inhibitor
Options selector
Catalog no. Size
SIH-117A 1 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 1 mg.
  • Lead time: options listed as “in stock at manufacturer” typically ship in 2-3 business days; other statuses may take longer.
  • Storage: -20ºC
  • Shipping: ships at ambient temperature.
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Mfr No SIH-117
Activity
  • Inhibitor
Cas No. 12772-57-5
Form White to Yellow Solid
Molecular Weight 364.8
Product Type
  • Biochemicals
  • Small Molecules
Purity 97% by TLC
Shipping Shipped Ambient
SMILES COc1ccc2c(=O)c(coc2c1OC)c3cc(c(cc3I)OC)OC
Solubility Soluble in DMSO
Source Produced by fermentation
Storage -20ºC

Radicicol is a macrocyclic antifungal compound that functions as a potent inhibitor of HSP90, a molecular chaperone involved in protein folding and stability. In neuroscience, Radicicol’s ability to bind HSP90 and disrupt its interaction with client proteins offers a mechanism for modulating neurodegenerative disease pathways. It selectively depletes kinases such as Raf and inhibits src-like kinases, contributing to the regulation of cellular stress responses and apoptosis. Radicicol also exhibits anti-angiogenic properties and induces morphological reversion in transformed cells, which may be relevant in neuro-oncology. Its strong binding affinity to HSP90 across species, including yeast and bacterial homologs, underscores its utility in translational research models. By targeting chaperone-mediated proteostasis, Radicicol holds promise for therapeutic intervention in disorders characterized by protein misfolding and aggregation.

Classification: Caution: Substance not yet fully tested.

Safety Phrases:

  • S22 - Do not breathe dust
  • S24/25 - Avoid contact with skin and eyes
  • S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection

Radicicol (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-117)

Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.

  • Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
  • Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
  • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
  • QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
  • Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity

To quote quickly, tell us: compound name + CAS/structure (SMILES or mol file), intended assay context, solvent preference, salt/stereochemistry requirements, purity/QC level, and the amount (mg–g).

Can’t find the compound you’re looking for?
Send the CAS or structure and your specs. We can help source it, suggest close equivalents, or discuss custom synthesis with the right QC documentation (RUO).

1. Kwon H.J., et al. (1992) Cancer Res. 52: 6929.
2. Yen A., et al. (1994) Exp.Cell Res. 214: 163.
3. Kwon H.J., et al. (1995) J.Biochem.(Tokyo) 118: 221.
4. Soga S., et al. (1998) J.Biol.Chem. 273: 822.
5. Oikawa T., et al. (1993) Eur.J.Pharmacol. 241: 221.
6. Roe S.M. et al. (1999) J.Med.Chem. 42: 260.

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