合成目标产物 Uridine-5'-Triphosphoric Acid Trisodium Salt 主要起始原料 Ump
(文献来源)合成步骤主要原料 Ump
专利信息
专利号:US-2025243525-A1 优先权日:2022-06-24 标 题 :Biocatalytic manufacture of sugar nucleotides 发明人:HOEPKER ALEXANDER CHRIS; CILA MEGHA; GISKA FABIAN 权利人:ZYMTRONIX CATALYTIC SYSTEMS INC 摘要:The invention provides the production of sugar-nucleotides and the isolation of sugar-nucleotides. In some embodiments the production or isolation are accomplished under acidic conditions. The production is a cell-free synthesis using enzymes, including immobilized enzymes. They may be accomplished using a one-pot reaction protocol. The synthesis may be used as a highly customizable and highly efficient cell-free manufacturing process. In some embodiments, the sugar-nucleotides are used to prepare UDP-Gal, lactose derivatives, and human milk oligosaccharides (HMOs).
专利号:US-8193338-B2 优先权日:2006-07-26 标题:Process for producing di(pyrimidine nucleoside 5'-)polyphosphate 发明人:KOGO SATORU; YAMADA KOHEI; IWAI YUKO; OSAWA KAZUOMI; HAYAKAWA HIROYUKI 权利人:KOGO SATORU; YAMADA KOHEI; IWAI YUKO; OSAWA KAZUOMI; HAYAKAWA HIROYUKI; YAMASA CORP 摘要:A di(pyrimidine nucleoside 5′-)polyphosphate is synthesized by converting a pyrimidine nucleoside 5′-triphosphate into a pyrimidine nucleoside 5′-cyclic triphosphate by use of a condensing agent, and subsequently reacting the pyrimidine nucleoside 5′-cyclic triphosphate with a pyrimidine nucleotide in the presence of a salt of a metal selected from among magnesium, manganese, and iron. Through the method of the invention, a di(pyrimidine nucleoside 5′-)polyphosphate can be synthesized from an unprotected pyrimidine nucleoside 5′-phosphate serving as a starting material at a synthesis yield of 50% or higher. Therefore, the method of the invention is suitable for large-scale synthesis of a di(pyrimidine nucleoside 5′-)polyphosphate.
1: Choi, J.H., Ji, Y.G., and Lee, D.H. Uridine triphosphate increases proliferation of human cancerous pancreatic duct epithelial cells by activating P2Y2 receptor. Pancreas 42(4), 680-686 (2013). 2: Maruoka, H., Jayasekara, M.P.S., Barrett, M.O., et al. Pyrimidine nucleotides with 4-alkyloxyimino and terminal tetraphosphate δ-ester modifications as selective agonists of the P2Y4 receptor. J. Med. Chem. 54(12), 4018-4033 (2011). 3: Matsumoto, T., Nakane, T., and Chiba, S. UTP induces vascular responses in the isolated and perfused canine epicardial coronary artery via UTP-preferring P2Y receptors. Br. J. Pharmacol. 122(8), 1625-1632 (1997).
合成参考文献
摘要:S10 | SWISSPHARMA | Pharmaceutical List with Consumption Data | DOI:10.5281/zenodo.2623484