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Small Targeted Cytotoxics: Current State and Promises from DNA-Encoded Chemical Libraries
被引:125
|作者:
Krall, Nikolaus
[1
]
Scheuermann, Joerg
[1
]
Neri, Dario
[1
]
机构:
[1] Swiss Fed Inst Technol, Swiss Fed Inst Technol Zurich, Inst Pharmaceut Sci, Dept Chem & Appl Biosci, CH-8093 Zurich, Switzerland
基金:
中国国家自然科学基金;
关键词:
cancer;
DNA-encoded libraries;
drug conjugates;
drug delivery;
prodrugs;
HORMONE-RELEASING HORMONE;
IN-VITRO SELECTION;
RECEPTOR-MEDIATED ENDOCYTOSIS;
ANTIBODY-DRUG CONJUGATE;
BOMBESIN ANALOG AN-215;
ED-B DOMAIN;
FOLATE-RECEPTOR;
MEMBRANE ANTIGEN;
ANTITUMOR-ACTIVITY;
PROSTATE-CANCER;
D O I:
10.1002/anie.201204631
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The targeted delivery of potent cytotoxic agents has emerged as a promising strategy for the treatment of cancer and other serious conditions. Traditionally, antibodies against markers of disease have been used as drug-delivery vehicles. More recently, lower molecular weight ligands have been proposed for the generation of a novel class of targeted cytotoxics with improved properties. Advances in this field crucially rely on efficient methods for the identification and optimization of organic molecules capable of high-affinity binding and selective recognition of target proteins. The advent of DNA-encoded chemical libraries allows the construction and screening of compound collections of unprecedented size. In this Review, we survey developments in the field of small ligand-based targeted cytotoxics and show how innovative library technologies will help develop the drugs of the future.
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页码:1384 / 1402
页数:19
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