DO264 | ABHD12 inhibitor
NMR (Conforms)
Available Options
| Size: | Price | Quantity | |
|---|---|---|---|
| 5 mg | $70.00 | ||
| 25 mg | $280.00 |
DO264 (2301866-59-9) is a potent, reversible competitive inhibitor of ABHD12 (α/β-hydrolase domain-containing 12) which shows negligible interaction with other serine hydrolases as determined by activity-based protein profiling.1 The IC50 of DO264 was determined to be 11 nM in isolated enzyme assays and it was shown to be active in vivo and brain penetrant. The compound was shown to produce significant elevation of brain lyso-PS/PI and C20:4 PS content in mice.2 THP-1 macrophages show increased cytokine production and mice show exacerbated immune responses to LCMV infection after treatment with DO264.1,2 Cellular studies should be limited to a concentration of 1 µM which is sufficient to fully inhibit ABDH12 and avoid cytotoxicity.1 Treatment of mice may be done at 30 mg/Kg po or ip with no overt signs of toxicity.1
References/Citations:
1) Ogasawara et al. (2019), Discovery and Optimization of Selective and in Vivo Active Inhibitors of the Lysophosphatidylserine Lipase α/β-Hydrolase Domain-Containing 12 (ABHD12); J. Med. Chem., 62 1643
2) Ogasawara et al. (2018), Selective Blockade of the Lyso-PS Lipase ABHD12 Stimulates Immune Responses In Vivo; Nat. Chem. Biol., 14 1099
NMR (Conforms)
Safety Data Sheet:
Product Data Sheet:
Materials provided by Focus Biomolecules are for laboratory research use only and are not intended for human or veterinary applications. Please note that we do not sell to individuals and that all orders placed by non-research organizations will incur a $20 restocking/refund fee
DO264 (2301866-59-9) is a potent, reversible competitive inhibitor of ABHD12 (α/β-hydrolase domain-containing 12) which shows negligible interaction with other serine hydrolases as determined by activity-based protein profiling.1 The IC50 of DO264 was determined to be 11 nM in isolated enzyme assays and it was shown to be active in vivo and brain penetrant. The compound was shown to produce significant elevation of brain lyso-PS/PI and C20:4 PS content in mice.2 THP-1 macrophages show increased cytokine production and mice show exacerbated immune responses to LCMV infection after treatment with DO264.1,2 Cellular studies should be limited to a concentration of 1 µM which is sufficient to fully inhibit ABDH12 and avoid cytotoxicity.1 Treatment of mice may be done at 30 mg/Kg po or ip with no overt signs of toxicity.1
References/Citations:
1) Ogasawara et al. (2019), Discovery and Optimization of Selective and in Vivo Active Inhibitors of the Lysophosphatidylserine Lipase α/β-Hydrolase Domain-Containing 12 (ABHD12); J. Med. Chem., 62 1643
2) Ogasawara et al. (2018), Selective Blockade of the Lyso-PS Lipase ABHD12 Stimulates Immune Responses In Vivo; Nat. Chem. Biol., 14 1099
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