CAS: 18542-37-5; Dl-Vernolepin

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    专利信息


    专利号:US-11851651-B2
    优先权日:2017-06-19
    标 题 :Automated methods for scalable, parallelized enzymatic biopolymer synthesis and modification using microfluidic devices
    发明人:BANAL JAMES; BERLEANT JOSEPH DON; SHEPHERD TYSON; BATHE MARK
    权利人:MASSACHUSETTS INST TECHNOLOGY
    摘要:Methods for the automated template-free synthesis of user-defined sequence controlled biopolymers using microfluidic devices are described. The methods facilitate simultaneous synthesis of up to thousands of uniquely addressed biopolymers from the controlled movement and combination of regents as fluid droplets using microfluidic and EWOD-based systems. In some forms, biopolymers including nucleic acids, peptides, carbohydrates, and lipids are synthesized from step-wise assembly of building blocks based on a user-defined sequence of droplet movements. In some forms, the methods synthesize uniquely addressed nucleic acids of up to 1,000 nucleotides in length. Methods for adding, removing and changing barcodes on biopolymers are also provided. Biopolymers synthesized according to the methods, and libraries and databases thereof are also described. Modified biopolymers, including chemically modified nucleotides and biopolymers conjugated to other molecules are described.

    专利号:US-2010317886-A1
    优先权日:2009-06-11
    标 题 :Synthesis of isotopically-labeled functionalized dienes
    发明人:MARTINEZ RODOLFO A
    权利人:MARTINEZ RODOLFO A
    摘要:All labeled carbons are derived ultimately from CO, as carbon-13 is separated from its lighter isotope by cyrogenic distillation of carbon monoxide (CO). Creation of stereospecific and site-specific compounds used for starting materials will address growing demands for labeled compounds, including isotopically-labeled functionalized dienes. Functionalized diene compounds can be used as precursors for the production of isotopically labeled pharmaceuticals, biomolecules, and natural products.

    专利号:BE-856002-A
    优先权日:1977-06-22
    标题:PREPARATION OF STARTING MATERIALS WITH 2-OXA-3-DECALON SKELETON FOR THE SYNTHESIS OF VERNOLEPIN-LIKE TUMOR GROWTH INHIBITORS

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    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Thongnest S, Chawengrum P, Keeratichamroen S, Lirdprapamongkol K, Eurtivong C, Boonsombat J, Kittakoop P, Svasti J, Ruchirawat S. Vernodalidimer L, a sesquiterpene lactone dimer from Vernonia extensa and anti-tumor effects of vernodalin, vernolepin, and vernolide on HepG2 liver cancer cells. Bioorg Chem. 2019 Aug 16;92:103197. doi: 10.1016/j.bioorg.2019.103197. [Epub ahead of print] pii: E2110. doi: 10.3390/molecules24112110.
    3: Kimani NM, Matasyoh JC, Kaiser M, Brun R, Schmidt TJ. Anti-Trypanosomatid Elemanolide Sesquiterpene Lactones from Vernonia lasiopus O. Hoffm. Molecules. 2017 Apr 8;22(4). pii: E597. doi: 10.3390/molecules22040597.
    4: Bach SM, Díaz FR, Bach H, Catalán CA. A facile and efficient four-step enantioselective synthesis of (+)-vernolepin from (+)-minimolide, the major germacranolide of Mikania minima. Nat Prod Commun. 2011 Apr;6(4):433-8.

    合成参考文献


    参考文献:10.1055/s-0040-1705991
    摘要:Wipf P, Nguyen TT. Intramolecular Diels–Alder Reactions of Oxazoles, Imidazoles, and Thiazoles. Synthesis. 2020 Dec 14;53(07):1181–99. doi: 10.1055/s-0040-1705991.
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