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通过加速硫酰氟交换点击化学实现功能库的模块化合成。

Modular synthesis of functional libraries by accelerated SuFEx click chemistry.

作者信息

Homer Joshua A, Koelln Rebecca A, Barrow Andrew S, Gialelis Timothy L, Boiarska Zlata, Steinohrt Nikita S, Lee Erinna F, Yang Wen-Hsuan, Johnson Robert M, Chung Taemoon, Habowski Amber N, Vishwakarma Dharmendra S, Bhunia Debmalya, Avanzi Charlotte, Moorhouse Adam D, Jackson Mary, Tuveson David A, Lyons Scott K, Lukey Michael J, Fairlie W Douglas, Haider Shozeb M, Steinmetz Michel O, Prota Andrea E, Moses John E

机构信息

Cancer Center, Cold Spring Harbor Laboratory 1 Bungtown Rd Cold Spring Harbor NY 11724 USA

La Trobe Institute for Molecular Science, La Trobe University Melbourne VIC 3086 Australia.

出版信息

Chem Sci. 2024 Mar 4;15(11):3879-3892. doi: 10.1039/d3sc05729a. eCollection 2024 Mar 13.

Abstract

Accelerated SuFEx Click Chemistry (ASCC) is a powerful method for coupling aryl and alkyl alcohols with SuFEx-compatible functional groups. With its hallmark favorable kinetics and exceptional product yields, ASCC streamlines the synthetic workflow, simplifies the purification process, and is ideally suited for discovering functional molecules. We showcase the versatility and practicality of the ASCC reaction as a tool for the late-stage derivatization of bioactive molecules and in the array synthesis of sulfonate-linked, high-potency, microtubule targeting agents (MTAs) that exhibit nanomolar anticancer activity against multidrug-resistant cancer cell lines. These findings underscore ASCC's promise as a robust platform for drug discovery.

摘要

加速硫氟交换点击化学(ASCC)是一种将芳基和烷基醇与硫氟交换兼容官能团偶联的强大方法。凭借其标志性的良好动力学和出色的产物收率,ASCC简化了合成工作流程,简化了纯化过程,非常适合发现功能分子。我们展示了ASCC反应作为生物活性分子后期衍生化工具以及用于合成具有纳摩尔级抗多药耐药癌细胞系抗癌活性的磺酸盐连接的高效微管靶向剂(MTA)阵列的多功能性和实用性。这些发现突出了ASCC作为药物发现强大平台的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97f0/10935723/332a8fa1c909/d3sc05729a-f1.jpg

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