Dipalmitin (Highly Pure)

<strong>Dipalmitin (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2018210_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 50 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 568.91_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20℃_x000D_ <strong>Keywords:</strong> Glycerol 1,2(3)-dihexadecanoate_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Ryu EK, Ross RJ, Matsushita T, MacCoss M, Hong CI, West CR. Phospholipid-nucleoside conjugates. 3. Syntheses and preliminary biological evaluation of 1-beta-D-arabinofuranosylcytosine 5'-monophosphate-L-1,2-dipalmitin and selected 1-beta-D-arabinofuranosylcytosine 5-diphosphate-L-1,2-diacylglycerols J Med Chem. 1982 Nov;25(11):1322-9._x000D_ 2: Pallas NR, Pethica BA. Lateral intermolecular forces between biomembrane lipids in two dimensions: 1,2-dipalmitin at the heptane/water interface compared with phospholipids J Phys Chem B. 2007 Jan 11;111(1):74-80._x000D_ 3: MacCoss M, Ryu EK, Matsushita T. The synthesis, characterization, and preliminary biological evaluation of 1-beta-D-arabinofuranosylcytosine-5'-diphosphate-L-1,2-dipalmitin Biochem Biophys Res Commun. 1978 Nov 29;85(2):714-23._x000D_ 4: Matsushita T, Ryu EK, Hong CI, MacCoss M. Phospholipid derivatives of nucleoside analogs as prodrugs with enhanced catabolic stability Cancer Res. 1981 Jul;41(7):2707-13._x000D_ 5: Rahman YE, Patel KR, Cerny EA, Maccoss M. The treatment of intravenously implanted Lewis lung carcinoma with two sustained release forms of 1-beta-D-arabinofuranosylcytosine Eur J Cancer Clin Oncol. 1984 Aug;20(8):1105-12._x000D_ 6: Fahey DA, Small DM. Surface properties of 1,2-dipalmitoyl-3-acyl-sn-glycerols Biochemistry. 1986 Jul 29;25(15):4468-72._x000D_ 7: Chen XS, Chen DH, Si JY, Tu GZ. Chemical constituents of Typhonium giganteum Engl J Asian Nat Prod Res. 2001;3(4):277-83._x000D_ 8: Ábrego-García A, Poggi-Varaldo HM, Ponce-Noyola MT, Calva-Calva G, Galíndez-Mayer CJJ, Medina-Mendoza GG, Rinderknecht-Seijas NF. Bioprocessing of Two Crop Residues for Animal Feeding into a High-Yield Lovastatin Feed Supplement Animals (Basel). 2022 Oct 7;12(19):2697._x000D_ 9: Pollack JD, Clark DS, Somerson NL. Four-directional-development thin-layer chromatography of lipids using trimethyl borate J Lipid Res. 1971 Sep;12(5):563-9._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/2160332">10: Kodali DR, Tercyak A, Fahey DA, Small DM. Acyl migration in 1,2-dipalmitoyl-sn-glycerol Chem Phys Lipids. 1990 Feb;52(3-4):163-70. </a>_x000D_ _x000D_ <strong>Products Related to Dipalmitin (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals /"> Chemicals </a>