 |  | | | | | (R)-Bromoenol lactone-d7 | Phospholipase | | Reference 10534 |  |
| | | Data |  | Molecular Formula | C16H6BrD7O2 |  | Formulation | A solution in methyl acetate |  | Purity | ≥99% deuterated product |  | Stability | 1 year |  | Storage | -20°C |  | Shipping | Wet Ice |  | Correlated Keywords | selective, iPLA2, inhibitors, phospholipases, PLAs, BEL, iPLA2b, iPLA2β, iPLA2g, iPLA2γ, lipids, hydrolases, cells, signaling, digestion, membrane, remodeling, venom, calcium, independent, releases, AA, arachidonic, acids, physiologic, stimuli, irreversible, chiral, mechanism-based, human, recombinants, deuterium, deuterateds, GC/MS, LC/MS, LC-MS, GC-MS, mass, spectrometry, MS, signalling, standards |  | Synonyms | (R)-BEL-d7 |
| | | Description | (R)-Bromoenol lactone-d7 ((R)-BEL-d7) contains seven deuterium atoms at the 2, 3, 4, 5, 6, 7, and 8 positions. It is intended for use as an internal standard for the quantification of (R)-BEL by GC- or LC-mass spectrometry (MS). The phospholipases are an extensive family of lipid hydrolases that function in cell signaling, digestion, membrane remodeling, and as venom components. The calcium-independent phospholipase A2 (iPLA2) are a PLA2 subfamily closely associated with the release of arachidonic acid in response to physiologic stimuli. (R)-Bromoenol lactone ((R)-BEL) is an irreversible, chiral, mechanism-based inhibitor of iPLA2γ. Unlike (S)-BEL, (R)-BEL does not inhibit iPLA2β except at high doses of 20-30 µM. (R)-BEL inhibits human recombinant iPLA2γ with an IC50 of approximately 0.6 µM. | | | Related Products | | | | Documentation | | | | |  | Jenkins, C.M., Han, X., Mancuso, D.J., et al. Identification of calcium-independent phospholipase A2 (iPLA2)β, and not iPLA2γ, as the mediator of arginine vasopressin-induced arachidonic acid release in A-10 smooth muscle cells. J Biol Chem 277(36) 32807-32814 (2002). |  | Balsinde, J., Balboa, M.A., Insel, P.A., et al. Regulation and inhibition of phospholipase A2. Annu Rev Pharmacol Toxicol 39 175-189 (1999). |
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