Synthesis and identification of unprecedented selective inhibitors of CK1ε-Reference-Cited by-同舟云学术

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Synthesis and identification of unprecedented selective inhibitors of CK1ε

Published:2015-05 Issue: Volume:96 Page:308-317
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Silveira-Dorta Gastón,Sousa Inês J.,Fernandes Miguel X.,Martín Victor S.,Padrón José M.^ORCID

Funder

EU Research Potential

European Regional Development Fund (FEDER)

Spanish MINECO

Instituto de Salud Carlos III

EU Social Fund (FSE)

ACIISI

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference45 articles.

1. Biodiversity of sphingoid bases (“sphingosines”) and related amino alcohols;Pruett;J. Lipid Res.,2008

2. Sphingolipid homeostasis in the web of metabolic routes;Aguilera-Romero;Biochim. Biophys. Acta,2014

3. Sphingolipids in anticancer therapy;Padrón;Curr. Med. Chem.,2006

4. Natural products to drugs: natural product derived compounds in clinical trials;Butler;Nat. Prod. Rep.,2005

5. Pachastrissamine, a cytotoxic an hydrophytosphingosine from a marine sponge, Pachastrissa sp;Kuroda;J. Nat. Prod.,2002

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2. Structure-Based Development of Isoform-Selective Inhibitors of Casein Kinase 1ε vs Casein Kinase 1δ;Journal of Medicinal Chemistry;2023-05-19

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