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Oridonin is a covalent NLRP3 inhibitor with strong anti-inflammasome activity. Oridonin (NSC-250682) also acts as an inhibitor of AKT, with IC50 values of 8.4 and 8.9 μM for AKT1 and AKT2, respectively.
Oridonin (10 or 20 μM) causes G2/M phase cell cycle arrest in KYSE70, KYSE410 and KYSE450 cells, and induces apoptosis in these three cell lines at 20 μM. In addition, Oridonin (5, 10 or 20 μM) in combination with cisplatin or 5-FU enhances the inhibition of esophageal squamous cell carcinoma (ESCC) cell growth.
| Molecular Weight | 364.44 |
| Formula | C20H28O6 |
| CAS Number | 28957-04-2 |
| Solubility (25°C) | DMSO 60 mg/mL |
| Storage | 4°C, dry, sealed |
[1] Xiang Li, et al. Oridonin: A Review of Its Pharmacology, Pharmacokinetics and Toxicity
[3] Yuanyuan Zhang, et al. Solubility and Bioavailability Enhancement of Oridonin: A Review
[5] Hongbin He, et al. Oridonin is a covalent NLRP3 inhibitor with strong anti-inflammasome activity
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