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Angew Chem Int Ed Engl. 2017 Aug 21;56(35):10294-10323. doi: 10.1002/anie.201611914. Epub 2017 Jul 24.

New Modalities for Challenging Targets in Drug Discovery.

Author information

1
Cardiovascular and Metabolic Diseases, Innovative Medicines and Early Development Biotech Unit, AstraZeneca, Pepparedsleden 1, Mölndal, 431 83, Sweden.
2
AstraZeneca MPI Satellite Unit, Abteilung Chemische Biologie, Max Planck Institut für Molekulare Physiologie, Dortmund, Germany.
3
Abteilung Chemische Biologie, Max Planck Institut für Molekulare Physiologie, Dortmund, Germany.
4
Fakultät für Chemie und Chemische Biologie, Technische Universität Dortmund, Germany.
5
Chemical Genomics Centre of the Max Planck Society, Dortmund, Germany.
6
Department of Chemistry & Pharmaceutical Sciences, VU University Amsterdam, The Netherlands.

Abstract

Our ever-increasing understanding of biological systems is providing a range of exciting novel biological targets, whose modulation may enable novel therapeutic options for many diseases. These targets include protein-protein and protein-nucleic acid interactions, which are, however, often refractory to classical small-molecule approaches. Other types of molecules, or modalities, are therefore required to address these targets, which has led several academic research groups and pharmaceutical companies to increasingly use the concept of so-called "new modalities". This Review defines for the first time the scope of this term, which includes novel peptidic scaffolds, oligonucleotides, hybrids, molecular conjugates, as well as new uses of classical small molecules. We provide the most representative examples of these modalities to target large binding surface areas such as those found in protein-protein interactions and for biological processes at the center of cell regulation.

KEYWORDS:

drug conjugates; macrocycles; oligonucleotides; peptides

PMID:
28186380
DOI:
10.1002/anie.201611914
[Indexed for MEDLINE]

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