CAS: 1255942-06-3; 3-Amino-1-(11,12-Didehydrodibenz[b,F]Azocin-5(6H)-yl)-1-Propanone

结构式图片

相似化合物

1539290-74-8 1337920-23-6 2007915-94-6

欧盟法规

C&L通报

合成工艺路线路线简述

  • 合成目标产物 Dbco-Amine 主要起始原料 5-Dibenzosuberenone
  • (文献来源)合成步骤主要原料 5-Dibenzosuberenone
5-二苯并环庚烯酮置于吡啶,Lithium Aluminium Tetrahydride,盐酸羟胺,Potassium Tert-Butylate,Pyridinium Hydrobromide Perbromide,Potassium Carbonate体系中,用 四氢呋喃,二氯甲烷,水 用作溶剂,化学反应 3.0H,反应生成氮杂二苯并环辛炔胺
参考文献:一种基于click反应的car-T细胞药物递送平台及其构建方法与应用
标题:一种基于click反应的car-T细胞药物递送平台及其构建方法与应用
摘要:本发明公开了一种基于click反应的car‑t细胞药物递送平台及其构建方法与应用,其是由负载药物的烯/炔基工具分子和表达至car‑t细胞表面的叠氮基寡糖发生click反应形成.本发明优点包括:以car‑t细胞为基础,通过click反应键合载药纳米颗粒与car‑t细胞,构建一种新的药物递送平台,增强药物疗效,减少了药物的毒副作用,为car‑t细胞在药物递送平台领域的应用提供了理论和实践基础.

海关参考信息

专利信息


专利号:US-2022411860-A1
优先权日:2015-09-28
标题:Design and synthesis of novel disulfide linker based nucleotides as reversible terminators for dna sequencing by synthesis

专利号:US-2023160000-A1
优先权日:2015-09-28
标 题:Synthesis of novel disulfide linker based nucleotides as reversible terminators for dna sequencing by synthesis

专利号:US-12018097-B2
优先权日:2017-06-09
标题 :Non-chromatographic purification of macrocyclic peptides by a resin catch and release
发明人:CREECH GARDNER S; KHEIRABADI MAHBOUBEH; EASTGATE MARTIN D; NIRSCHL DAVID S; CARTER PERCY H
权利人:BRISTOL MYERS SQUIBB CO
摘要:The disclosure is directed to the synthesis and improved methods for purifying macrocyclic peptides produced by solid phase peptide synthesis. The synthesized peptide is capped with an alkyne-functionalized or azide-functionalized compound of formula (I):prior to cleavage of the peptide from the solid phase support.

专利号:US-2023028388-A1
优先权日:2015-09-28
标 题 :Design and synthesis of novel disulfide linker based nucleotides as reversible terminators for dna sequencing by synthesis

专利号:US-2022401561-A1
优先权日:2019-09-30
标题 :Protein-macromolecule conjugates and methods of use thereof
发明人:SONG YUNTAO; LI HUI; ZHOU HAIPING; LIAO CHUAN
权利人:BEIJING XUANYI PHARMASCIENCES CO LTD
摘要:The present disclosure provides protein-macromolecule conjugates, releasable linkers, and macromolecules, as defined herein. The disclosed conjugates provide unique properties that ae based at least upon the properties of linker and number of linker-Macromolecule moieties. Also provided herein are a method of synthesis and use of conjugates in treating diseases and disorders.

专利号:US-11725224-B2
优先权日:2018-04-16
标题 :Methods for co-activating in vitro non-standard amino acid (nsAA) incorporation and glycosylation in crude cell lysates
发明人:JEWETT MICHAEL CHRISTOPHER; STARK JESSICA CAROL; HERSHEWE JASMINE
权利人:UNIV NORTHWESTERN
摘要:Disclosed are methods, systems, components, and compositions for cell-free synthesis of proteins and glycoproteins. The methods, systems, components, and compositions may be utilized for incorporating non-standard amino acids (nsAAs) into cell-free synthesized proteins and glycosylating or otherwise modifying the cell-free synthesized proteins in vitro. The nsAAs of the cell-free synthesized protein may be modified via glycosylation or other modification.
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主要参考文献


1: Wang H, Tang L, Liu Y, Dobrucka IT, Dobrucki LW, Yin L, Cheng J. In Vivo Targeting of Metabolically Labeled Cancers with Ultra-Small Silica Nanoconjugates. Theranostics. 2016 Jun 16;6(9):1467-76. doi: 10.7150/thno.16003. eCollection 2016.
2: Yoon HI, Yhee JY, Na JH, Lee S, Lee H, Kang SW, Chang H, Ryu JH, Lee S, Kwon IC, Cho YW, Kim K. Bioorthogonal Copper Free Click Chemistry for Labeling and Tracking of Chondrocytes In Vivo. Bioconjug Chem. 2016 Apr 20;27(4):927-36. doi: 10.1021/acs.bioconjchem.6b00010. Epub 2016 Mar 10. doi: 10.1021/bc400490z. Epub 2014 Jan 29.

合成参考文献


摘要:Friscourt, F., Science of Synthesis, (2021) , 646.
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