CAS: 70539-42-3; Bis(2,5-Dioxopyrrolidin-1-yl) O,O'-Ethane-1,2-Diyl Disuccinate

该化合物是合成有机化合物,其结构复杂,包括一个乙基脊柱和由四氧丁酸衍生的两酯功能组,其存在表明它有可能在药用化学中,特别是在药物设计中应用,因为它能够形成氢联结并与生物目标相互作用.这种化合物有可能在有机溶剂中表现出中等溶性,而其极地功能组可能提高极地溶剂的溶性.其分子结构表明它具有潜在的再活动性,特别是在酯化和水解反应方面.此外,该化合物可能具有有趣的热和化学稳定性特性,因此它适合于材料科学和药物的各种应用.如同许多合成化合物一样,安全数据和处理预防措施应予考虑,因为其具体的毒性和环境影响将取决于其浓度和接触途径.

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30364-60-4 1008402-79-6 1334170-02-3

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    专利号:US-10254287-B2
    优先权日:2015-07-21
    标题 :Protein fluorescent nanoparticles and methods of synthesis thereof
    发明人:KUMAR CHALLA VIJAYA; STROMER BOBBI SHANYELLE
    权利人:UNIV CONNECTICUT
    摘要:Disclosed herein are stable and versatile protein nanoparticles having a range of tunable fluorescent properties. Such nanoparticles may find utility in biological imaging. Methods of synthesis of such nanoparticles are also disclosed.

    专利号:WO-9518971-A1
    优先权日:1994-01-11
    标 题 :Methods for the solid phase synthesis of glycoconjugates
    发明人:VETTER DIRK; TUMELTY DAVID A; ANTONENKO VALERY
    权利人:AFFYMAX TECH NV; VETTER DIRK; TUMELTY DAVID A; ANTONENKO VALERY
    摘要:An efficient and versatile method of forming N-linked glycoconjugates is described wherein a glycosyl acceptor, typically comprising an activated carboxyl group, is reacted with a glycosylating agent, typically a glycosylamine, in the presence of a coupling catalyst and optionally an exogenous base. Depending on the choice of reactive site, this method can be utilized to form N-linked glycoconjugates, in either a soluble or substrate-bound, linear or branched format.

    专利号:US-2010247433-A1
    优先权日:2005-10-14
    标题:Use of non-canonical amino acids as metabolic markers for rapidly-dividing cells
    发明人:TIRRELL DAVID; DIETERICH DANIELA C; LINK AARON J; SCHUMAN ERIN
    权利人:CALIFORNIA INST OF TECHN
    摘要:The invention provides methods, reagents and systems to preferentially mark fast-proliferating cells/tissues (such as cancer), by incorporating non-natural amino acids into proteins, preferably in vivo, using the endogenous protein synthesis machinery of an organism. The incorporated non-natural amino acids contain reactive groups for further chemical reagents, which may serve as a “handleâ€? to for a number of uses, such as imaging of cancer cells, targeting drugs to preferentially kill cancer cells, and proteomic analysis in the context of large scale or high throughput screening for candidate drug leads that affects the proliferation of a target cell, etc.

    专利号:US-12195777-B2
    优先权日:2018-02-02
    标 题 :Polynucleotide synthesis method, kit and system
    发明人:HERON ANDREW JOHN
    权利人:OXFORD NANEPORE TECH PLC; OXFORD NANOPORE TECH PLC
    摘要:The invention relates to new in vitro methods for synthesising a polymer, particularly a polynucleotide molecule, having a pre-defined sequence of units such as nucleotides. For synthesising a polynucleotide molecule the methods involve a process of extending a polynucleotide synthesis molecule with a transfer nucleotide. The methods additionally involve repeating the extension process multiple times to iteratively extend the polynucleotide molecule with multiple transfer nucleotides to generate a new polynucleotide molecule having a pre-defined nucleotide sequence. The invention also relates to in vitro methods of joining multiple synthetic polynucleotides following synthesis to form larger synthetic polynucleotides, as well as devices and systems for performing the extension, synthesis and assembly methods of the invention.

    专利号:US-11472777-B2
    优先权日:2015-09-14
    标题:Piperazine and piperidine derivatives, their synthesis and use thereof in inhibiting VDAC oligomerization, apoptosis and mitochondria dysfunction
    发明人:SHOSHAN-BARMATZ VARDA; LEV GRUZMAN ARIE
    权利人:NAT INST BIOTECHNOLOGY NEGEV LTD
    摘要:Provided herein piperazine and piperidine derivatives, their synthesis and use thereof in inhibiting VDAC oligomerization, apoptosis and mitochondria dysfunction. Also provided methods of treatment of diseases associated with said processes, e.g. Alzheimer's and Parkinson's diseases.

    专利号:US-10508091-B2
    优先权日:2015-09-14
    标 题:Piperazine and piperidine derivatives, their synthesis and use thereof in inhibiting VDAC oligomerization, apoptosis and mitochondria dysfunction
    发明人:SHOSHAN-BARMATZ VARDA; LEV GRUZMAN ARIE
    权利人:NAT INST BIOTECHNOLOGY NEGEV LTD
    摘要:Provided herein piperazine and piperidine derivatives, their synthesis and use thereof in inhibiting VDAC oligomerization, apoptosis and mitochondria dysfunction. Also provided methods of treatment of diseases associated with said processes, e.g. Alzheimer's disease.

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    主要参考文献


    1: Dreiling A, Hanneken M, König S. Early cleavage of ethylene glycol bis(succinimidylsuccinate) (EGS)-linker moieties during enzymatic digestion of cross-linked proteins. Rapid Commun Mass Spectrom. 2014 Nov 15;28(21):2385-8. doi: 10.1002/rcm.7034. doi: 10.1088/1748-6041/10/6/065015.

    合成参考文献


    摘要:Compound: Poly(oxy-1,2-ethanediyl), α-[4-[(2,5-dioxo-1-pyrrolidinyl)oxy]-1,4-dioxobutyl]-ω-[4-[(2,5-dioxo-1-pyrrolidinyl)oxy]-1,4-dioxobutoxy]-
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