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别洛沙米定的高效合成及其生物活性

High-efficient synthesis and biological activities of allosamidins.

作者信息

Huang Gangliang, Peng Daquan, Mei Xinya, Chen Xin, Xiao Feng, Tang Qilin

机构信息

a College of Chemistry, Chongqing Normal University , Chongqing , China.

出版信息

J Enzyme Inhib Med Chem. 2015 Dec;30(6):863-6. doi: 10.3109/14756366.2014.987137. Epub 2014 Dec 8.

Abstract

The pseudo-trisaccharide allosamidin 1 is a potent inhibitor of all family-18 chitinases, and it is confirmed to have insecticidal and antifungal activities. But the synthesis of allosamidins is very difficult, and it is a challengeable subject. Allosamidins were synthesized in solid-liquid phase, total solid-phase and total liquid-phase, respectively. Solid-liquid phase method realizes the partial solid-phase synthesis of allosamidins. Total solid-phase method greatly simplifies the purification process. Total liquid-phase method shortens the synthetic steps of allosamidins. The insecticidal and antifungal activities of allosamidins were also reported herein.

摘要

假三糖别洛沙米定1是所有18族几丁质酶的有效抑制剂,并且已证实其具有杀虫和抗真菌活性。但是别洛沙米定的合成非常困难,是一个具有挑战性的课题。别洛沙米定分别通过固液相、全固相和全液相进行合成。固液相法实现了别洛沙米定的部分固相合成。全固相法极大地简化了纯化过程。全液相法缩短了别洛沙米定的合成步骤。本文还报道了别洛沙米定的杀虫和抗真菌活性。

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