Cholesteryl hemisuccinate Tris Salt

<strong>Cholesteryl hemisuccinate Tris Salt</strong>_x000D_ <strong>Catalog number:</strong> B2017942_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 1 g_x000D_ <strong>Molecular Weight or Concentration:</strong> 607.86 g/mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> −20°C_x000D_ <strong>Keywords:</strong> 3β-Hydroxy-5-cholestene 3-hemisuccinate, 5-Cholesten-3β-ol 3-hemisuccinate, CHEMS, CHS, Cholesteryl hydrogen succinate_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: Djuric Z, Heilbrun LK, Lababidi S, Everett-Bauer CK, Fariss MW. Growth inhibition of MCF-7 and MCF-10A human breast cells by alpha-tocopheryl hemisuccinate, cholesteryl hemisuccinate and their ether analogs Cancer Lett. 1997 Jan 1;111(1-2):133-9._x000D_ 2: Xu H, Deng Y, Chen D, Qin J, Liu J, Shi L, Lu Y. Preparation and characterization of pH-sensitive vesicles made of cholesteryl hemisuccinate Drug Dev Ind Pharm. 2008 Feb;34(2):134-41._x000D_ 3: Cornut D, Soulié M, Moreno A, Boussambe GNM, Damian M, Igonet S, Guillet P, Banères JL, Durand G. Non-ionic cholesterol-based additives for the stabilization of membrane proteins Biochimie. 2023 Feb;205:27-39._x000D_ 4: Fariss MW, Lippman HR, Mumaw VR, Ray SD. Cholesteryl hemisuccinate treatment protects rodents from the toxic effects of acetaminophen, adriamycin, carbon tetrachloride, chloroform and galactosamine Toxicol Lett. 1997 Feb 7;90(2-3):133-44._x000D_ 5: Fariss MW, Fortuna MB, Everett CK, Smith JD, Trent DF, Djuric Z. The selective antiproliferative effects of alpha-tocopheryl hemisuccinate and cholesteryl hemisuccinate on murine leukemia cells result from the action of the intact compounds Cancer Res. 1994 Jul 1;54(13):3346-51._x000D_ 6: Locatelli-Hoops SC, Gorshkova I, Gawrisch K, Yeliseev AA. Expression, surface immobilization, and characterization of functional recombinant cannabinoid receptor CB2 Biochim Biophys Acta. 2013 Oct;1834(10):2045-56._x000D_ 7: Xu H, Wang KQ, Deng YH, Chen DW. Effects of cleavable PEG-cholesterol derivatives on the accelerated blood clearance of PEGylated liposomes Biomaterials. 2010 Jun;31(17):4757-63._x000D_ 8: el Mestikawy S, Taussig D, Gozlan H, Emerit MB, Ponchant M, Hamon M. Chromatographic analyses of the serotonin 5-HT1A receptor solubilized from the rat hippocampus J Neurochem. 1989 Nov;53(5):1555-66._x000D_ 9: Charbe NB, Amnerkar ND, Ramesh B, Tambuwala MM, Bakshi HA, Aljabali AAA, Khadse SC, Satheeshkumar R, Satija S, Metha M, Chellappan DK, Shrivastava G, Gupta G, Negi P, Dua K, Zacconi FC. Small interfering RNA for cancer treatment: overcoming hurdles in delivery Acta Pharm Sin B. 2020 Nov;10(11):2075-2109._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/31674185">10: Augustyn B, Stepien P, Poojari C, Mobarak E, Polit A, Wisniewska-Becker A, Róg T. Cholesteryl Hemisuccinate Is Not a Good Replacement for Cholesterol in Lipid Nanodiscs J Phys Chem B. 2019 Nov 21;123(46):9839-9845. </a>_x000D_ _x000D_ <strong>Products Related to Cholesteryl hemisuccinate Tris Salt can be found at</strong> <a href="https://moleculardepot.com/product-category/Lipids/"> Lipids</a>