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The glycerol phosphate pathway starts with the reaction of G-3-P with fatty acid-coenzyme A (FA-CoA) to form lysophosphatidic acid (LPA) catalyzed by glycerol-3-phosphate acyltransferase (GPAT) [44]
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After reconstitution with bacteriostatic water or a suitable solvent, store at 28C and use within a limited timeframe
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A pharmacokinetic study in rats found that oral administration produced substantial plasma concentrations, with a maximum concentration of 2252 ng/mL and an elimination half-life of approximately 6.9 hours
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