نتایج جستجو برای: bioconjugation

تعداد نتایج: 645  

Journal: :Organic & biomolecular chemistry 2013
Lalit N Goswami Zachary H Houston Saurav J Sarma Satish S Jalisatgi M Frederick Hawthorne

Herein we describe the sequential synthesis of a variety of azide-alkyne click chemistry-compatible heterobifunctional oligo(ethylene glycol) (OEG) linkers for bioconjugation chemistry applications. Synthesis of these bioorthogonal linkers was accomplished through desymmetrization of OEGs by conversion of one of the hydroxyl groups to either an alkyne or azido functionality. The remaining dista...

Journal: :Bioconjugate chemistry 2011
Niraikulam Ayyadurai Nadarajan Saravanan Prabhu Kanagavel Deepankumar Yoon Jung Jang Nataraj Chitrapriya Eunjung Song Nahum Lee Seog K Kim Byung-Gee Kim Nagasundarapandian Soundrarajan Sungu Lee Hyung Joon Cha Nediljko Budisa Hyungdon Yun

We describe the simple bioconjugation strategy in combination of periodate chemistry and unnatural amino acid incorporation. The residue specific incorporation of 3,4-dihydroxy-l-phenylalanine can alter the properties of protein to conjugate into the polymers. The homogeneously modified protein will yield quinone residues that are covalently conjugated to nucleophilic groups of the amino polysa...

Journal: :Chemical communications 2015
Yang Xu Ling Xu Yuan Xia Chao-Jian Guan Qing-Xiang Guo Yao Fu Chen Wang Yi-Ming Li

Rapid and catalyst-free hydrazone ligation reaction between ortho-halobenzaldehyde derivatives and peptide/protein hydrazides was observed at neutral pH and room temperature. 2-Chlorobenzaldehyde exhibited the fastest reaction and highest conversion rates among the series of ortho-halobenzaldehydes. The resulting hydrazone-containing bioconjugation products were also found to be fairly stable u...

2017
Kun Shen Qiu Wang

A copper-catalyzed aminoalkynylation of alkenes is achieved with ethynylbenziodoxolone (EBX) reagents under mild conditions with only 1 mol% copper catalyst. This transformation allows for rapid construction of diverse important azahetereocycles and installation of valuable alkyne groups in one step. The developed method features remarkable substrate scope for both terminal and internal alkenes...

2012
Rong Tong Jianjun Cheng

Several Zn b-diiminate reagents were developed and used to mediate regioselective O-acylation reactions of therapeutic agents with anhydrides. Various prodrugs were obtained in excellent yield and high regioselectivity, including derivatives of rapamycin and paclitaxel. Furthermore, the application of regioselective acylation was extended to one-pot reactions between therapeutics and carboxylic...

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