| Field | Specification |
|---|---|
| Mfr No | |
| Activity | |
| Alternative Names | 7a,20-Epoxy-1a,6b,7,14-tetrahydroxykaur-16-en-15-one; Isodonol |
| Cas No. | |
| Form | White to off-white powder |
| Molecular Weight | |
| Product Type | |
| Purity | |
| Shipping | |
| SMILES | |
| Solubility | May be dissolved in DMSO (50 mg/ml); or Ethanol (10 mg/ml, warm) |
| Source | Synthetic |
| Storage |
Oridonin is a covalent inhibitor of the NLRP3 inflammasome with potent anti-inflammatory properties. It has demonstrated efficacy in reducing vascular inflammation and modulating PI3K/AKT signaling. In neurodegenerative disease research, Oridonin is being explored for its ability to suppress neuroinflammation, inhibit aberrant signaling pathways, and induce apoptosis in pathological cell populations.
Classification: Warning. Hazard Statements: H351. Precautionary Statements: P203, P280, P318, P405, and P501
Oridonin (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-624)
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).
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equivalents, or discuss custom synthesis with the right QC documentation (RUO).
2. Huang W., et al. (2018) Eur. J. Pharmacol. 826:133.
3. Sun B., et al. (2018) Oncotarget 9:23878.
4. Li CY., et al. (2018) Oncol. Lett. 15:1362.
5. Lu Y., et al. (2018) Cell Death Dis. 9:15.