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Designed as an analog of the PPARγ-binding prostaglandins which could not undergo this conjugation reaction. In human neuroblastoma SH-SY5Y cells, compound was not cytotoxic at up to 25 µM. Failed to covalently modify thioredoxin or induce oxidative stress at 50 µM.3
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
9,10-dihydro-15-deoxy-Δ12,14-Prostaglandin J2, 500 µg | sc-223760 | 500 µg | $91.00 | |||
9,10-dihydro-15-deoxy-Δ12,14-Prostaglandin J2, 1 mg | sc-223760A | 1 mg | $172.00 |