Rottlerin

SKU:BHB11900182
Suppliers
StressMarq Biosciences Inc.
StressMarq Biosciences Inc.
Details Products
Overview
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Rottlerin is a research-grade small-molecule inducer of autophagy supporting Cancer and Autophagy research. Supplied as a orange to brown solid. with 98% purity (CAS 82-08-6, MW 516.55) Soluble to 2 mM in ethanol and to 20 mM in DMSO.; store at -20°C. For research use only.
Cas No. 82-08-6
Molecular Formula C30H28O8
Purity ≥98%
Application Notes Autophagy inducer
Options selector
Catalog no. Size
SIH-394-10MG 10 mg
SIH-394-50MG 50 mg
Available Options

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

  • Options: Size (2) — 10 mg, 50 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-394
Activity
  • Inducer
Alternative Names 3'-[(8-Cinnamoyl-5,7-dihydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)methyl]-2',4',6'-trihydroxy-5'-methylacetophenone
Cas No. 82-08-6
Form Orange to brown solid.
Molecular Weight 516.55
Product Type
  • Biochemicals
  • Small Molecules
Purity ≥98%
Shipping Shipped Ambient
SMILES C1=CC=CC=C1/C=C/C(C2=C(C(=C(C3=C2OC(C)(C)C=C3)O)CC4=C(C(=C(C(=C4O)C(C)=O)O)C)O)O)=O
Solubility Soluble to 2 mM in ethanol and to 20 mM in DMSO.
Source Synthetic
Storage -20ºC

Rottlerin is a natural polyphenol known for its inhibitory effects on protein kinase C (PKC) and Ca²⁺/calmodulin-dependent kinase III. In neuroscience, Rottlerin is recognized for its neuroprotective properties, particularly in models of Parkinson’s disease. It acts as a mitochondrial uncoupler, depolarizing membrane potential and influencing energy metabolism. Rottlerin also induces autophagy by inhibiting mTORC1 signaling, a pathway critical for neuronal survival and protein clearance. Its ability to modulate potassium channels and reduce oxidative stress further supports its application in neurodegenerative disease research. Rottlerin is frequently used to explore the interplay between mitochondrial function, autophagy, and neuronal health.

Classification: Not WHMIS controlled.

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.

Rottlerin (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-394)

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. Gschwendt M. et al. (1994) Biochem Biophys Res Commun. 199(1): 93-8.
2. Wu S., et al. (2007) J Cell Physiol. 210(3): 655-66.
3. Soltoff S. (2001) J Biol Chem. 276(41): 37986-92.
4. Balgi A., et al. (2009) PLoS One. 4(9): e7124.

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