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1.
Chemistry ; 30(30): e202400611, 2024 May 28.
Article in English | MEDLINE | ID: mdl-38512657

ABSTRACT

Transition-metal-catalyzed bioorthogonal reactions emerged a decade ago as a novel strategy to implement spatiotemporal control over enzymatic functions and pharmacological interventions. The use of this methodology in experimental therapy is driven by the ambition of improving the tolerability and PK properties of clinically-used therapeutic agents. The preclinical potential of bioorthogonal catalysis has been validated in vitro and in vivo with the in situ generation of a broad range of drugs, including cytotoxic agents, anti-inflammatory drugs and anxiolytics. In this article, we report our investigations towards the preparation of solid-supported Cu(I)-microdevices and their application in bioorthogonal uncaging and click reactions. A range of ligand-functionalized polymeric devices and off-on Cu(I)-sensitive sensors were developed and tested under conditions compatible with life. Last, we present a preliminary exploration of their use for the synthesis of PROTACs through CuAAC assembly of two heterofunctional mating units.


Subject(s)
Click Chemistry , Copper , Copper/chemistry , Catalysis , Biocompatible Materials/chemistry , Alkynes/chemistry , Ligands , Polymers/chemistry , Humans , Azides/chemistry
2.
J Med Chem ; 65(2): 1047-1131, 2022 01 27.
Article in English | MEDLINE | ID: mdl-34624192

ABSTRACT

The central role of dysregulated kinase activity in the etiology of progressive disorders, including cancer, has fostered incremental efforts on drug discovery programs over the past 40 years. As a result, kinase inhibitors are today one of the most important classes of drugs. The FDA approved 73 small molecule kinase inhibitor drugs until September 2021, and additional inhibitors were approved by other regulatory agencies during that time. To complement the published literature on clinical kinase inhibitors, we have prepared a review that recaps this large data set into an accessible format for the medicinal chemistry community. Along with the therapeutic and pharmacological properties of each kinase inhibitor approved across the world until 2020, we provide the synthesis routes originally used during the discovery phase, many of which were only available in patent applications. In the last section, we also provide an update on kinase inhibitor drugs approved in 2021.


Subject(s)
Antineoplastic Agents/therapeutic use , Drug Approval , Neoplasms/drug therapy , Protein Kinase Inhibitors/therapeutic use , Small Molecule Libraries/therapeutic use , Antineoplastic Agents/chemical synthesis , Humans , Neoplasms/enzymology , Protein Kinase Inhibitors/chemical synthesis , Small Molecule Libraries/chemical synthesis , United States , United States Food and Drug Administration
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