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含酰胺分子释放方面的进展。

Advances in the Release of Amide-Containing Molecules.

作者信息

Wharton Thomas, Spring David R

机构信息

Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.

出版信息

Chemistry. 2025 Mar 17;31(16):e202404413. doi: 10.1002/chem.202404413. Epub 2025 Jan 28.

DOI:10.1002/chem.202404413
PMID:39836098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11914939/
Abstract

The ability to release a molecule from a larger construct in a controlled manner is of great importance to produce effective prodrugs, antibody-drug conjugates, and chemical probes. Amides are ubiquitous functional groups and yet methods to utilise them as molecular release handles are seldom reported. This concept article highlights the advances made in amide release strategies and how these approaches have been utilised.

摘要

以可控方式从较大构建体中释放分子的能力对于生产有效的前药、抗体药物偶联物和化学探针至关重要。酰胺是普遍存在的官能团,但将它们用作分子释放手柄的方法却鲜有报道。这篇概念文章重点介绍了酰胺释放策略方面取得的进展以及这些方法是如何被应用的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/d96c7f9e3a1a/CHEM-31-e202404413-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/557551e58225/CHEM-31-e202404413-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/bee1bd294484/CHEM-31-e202404413-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/025609b0fc67/CHEM-31-e202404413-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/b995184825a7/CHEM-31-e202404413-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/f5e1b3647f88/CHEM-31-e202404413-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/58deae6767f6/CHEM-31-e202404413-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/2b97637bf2cb/CHEM-31-e202404413-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/d96c7f9e3a1a/CHEM-31-e202404413-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/557551e58225/CHEM-31-e202404413-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/bee1bd294484/CHEM-31-e202404413-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/025609b0fc67/CHEM-31-e202404413-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/b995184825a7/CHEM-31-e202404413-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/f5e1b3647f88/CHEM-31-e202404413-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/58deae6767f6/CHEM-31-e202404413-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/2b97637bf2cb/CHEM-31-e202404413-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/11914939/d96c7f9e3a1a/CHEM-31-e202404413-g005.jpg

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本文引用的文献

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Chem Sci. 2024 Apr 2;15(16):6168-6177. doi: 10.1039/d4sc01576b. eCollection 2024 Apr 24.
2
Unlocking Amides: A General Method for the Self-Immolative Release of Amide-Containing Molecules.解锁酰胺:一种通用的自毁释酰胺分子的方法。
Angew Chem Int Ed Engl. 2024 Apr 24;63(18):e202402267. doi: 10.1002/anie.202402267. Epub 2024 Mar 27.
3
Exploration of the antibody-drug conjugate clinical landscape.
抗体药物偶联物临床全景探索。
MAbs. 2023 Jan-Dec;15(1):2229101. doi: 10.1080/19420862.2023.2229101.
4
Stimuli-Responsive PROTACs for Controlled Protein Degradation.刺激响应型 PROTAC 用于可控蛋白降解。
Angew Chem Int Ed Engl. 2023 Sep 25;62(39):e202306824. doi: 10.1002/anie.202306824. Epub 2023 Aug 17.
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Controlled Self-Assembly of Discrete Amphiphilic Oligourethanes with a Cascade Self-Immolative Motif.具有级联自牺牲基序的离散两亲性低聚脲烷的可控自组装。
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Angew Chem Int Ed Engl. 2022 Nov 21;61(47):e202203243. doi: 10.1002/anie.202203243. Epub 2022 Oct 25.
8
A pH-responsive crosslinker platform for antibody-drug conjugate (ADC) targeting delivery.一种用于抗体药物偶联物(ADC)靶向递药的 pH 响应型交联剂平台。
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