1-Oleoyl-sn-glycero-3-phosphocholine

<strong>1-Oleoyl-sn-glycero-3-phosphocholine</strong>_x000D_ <strong>Catalog number:</strong> B2017924_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 1 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 521.67_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> (7R,18Z)-4,7-Dihydroxy-N,N,N-trimethyl-10-oxo-3,5,9-trioxa-4-phosphaheptacos-18-en-1-aminium 4-oxide, inner salt, 1-(9Z-Octadecenoyl)-sn-glycero-3-phosphocholine, 1-cis-9-Octadecenoyl-sn-glycero-3-phosphocholine, 1-Oleoyl-2-hydroxy-sn-glycerol-3-phosphocholine, 1-Oleoyl-sn-glycero-3-phosphorylcholine, 3-sn-Lysophosphatidylcholine, 1-oleoyl, L-γ-Oleoyl-α-lysolecithin, Lysolecithin, oleoyl, PC(18:1(9Z)/0:0), PC(18:1/0:0)_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: Yasuda D, Hamano F, Masuda K, Dahlström M, Kobayashi D, Sato N, Hamakubo T, Shimizu T, Ishii S. Inverse agonism of lysophospholipids with cationic head groups at Gi-coupled receptor GPR82 Eur J Pharmacol. 2023 Sep 5;954:175893._x000D_ 2: Yue B, Zhang X, Li W, Wang J, Sun Z, Niu R. Fluoride exposure altered metabolomic profile in rat serum Chemosphere. 2020 Nov;258:127387._x000D_ 3: Su J, Li S, Chen J, Jian C, Hu J, Du H, Hai H, Wu J, Zeng F, Zhu J, Liu Y. Glycerophospholipid metabolism is involved in rheumatoid arthritis pathogenesis by regulating the IL-6/JAK signaling pathway Biochem Biophys Res Commun. 2022 Apr 16;600:130-135._x000D_ 4: Bessonneau V, Ings J, McMaster M, Smith R, Bragg L, Servos M, Pawliszyn J. In vivo microsampling to capture the elusive exposome Sci Rep. 2017 Mar 7;7:44038._x000D_ 5: Riessberger-Gallé U, Hernández-López J, Rechberger G, Crailsheim K, Schuehly W. Lysophosphatidylcholine acts in the constitutive immune defence against American foulbrood in adult honeybees Sci Rep. 2016 Aug 2;6:30699._x000D_ 6: Rouet-Mayer MA, Valentova O, Simond-Côte E, Daussant J, Thévenot C. Critical analysis of phospholipid hydrolyzing activities in ripening tomato fruits. Study by spectrofluorimetry and high-performance liquid chromatography Lipids. 1995 Aug;30(8):739-46._x000D_ 7: Foulds LM, Boysen RI, Crane M, Yang Y, Muir JA, Smith AI, de Kretser DM, Hearn MT, Hedger MP. Molecular identification of lyso-glycerophosphocholines as endogenous immunosuppressives in bovine and rat gonadal fluids Biol Reprod. 2008 Sep;79(3):525-36._x000D_ 8: Schmidt N, Gercken G. Synthesis of a fluorescent analogue of phosphatidylcholine Chem Phys Lipids. 1985 Sep;38(3):309-14._x000D_ 9: Ma W, Paik DC, Barile GR. Bioactive lysophospholipids generated by hepatic lipase degradation of lipoproteins lead to complement activation via the classical pathway Invest Ophthalmol Vis Sci. 2014 Sep 9;55(10):6187-93._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/7104401">10: Chaudhary LR. Subcellular distribution and some properties of acid phospholipase A1 in rat testis Biochimie. 1982 May;64(5):341-6. </a>_x000D_ _x000D_ <strong>Products Related to 1-Oleoyl-sn-glycero-3-phosphocholine can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals /"> Chemicals </a>