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Cdc-Like Kinases (CLKs): Biology, Chemical Probes, and Therapeutic Potential
P. Martín Moyano, V. Němec, K. Paruch
Language English Country Switzerland
Document type Journal Article, Review
Grant support
CZ.02.1.01/0.0/0.0/16_025/0007381
European Structural and Investment Funds, Operational Programme Research, Development and Education
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
33066143
DOI
10.3390/ijms21207549
Knihovny.cz E-resources
- MeSH
- Protein Kinase Inhibitors pharmacology therapeutic use MeSH
- Carcinogenesis drug effects metabolism MeSH
- Humans MeSH
- Protein Serine-Threonine Kinases antagonists & inhibitors chemistry genetics metabolism MeSH
- Antineoplastic Agents pharmacology therapeutic use MeSH
- Protein-Tyrosine Kinases antagonists & inhibitors chemistry genetics metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
Protein kinases represent a very pharmacologically attractive class of targets; however, some members of the family still remain rather unexplored. The biology and therapeutic potential of cdc-like kinases (CLKs) have been explored mainly over the last decade and the first CLK inhibitor, compound SM08502, entered clinical trials only recently. This review summarizes the biological roles and therapeutic potential of CLKs and their heretofore published small-molecule inhibitors, with a focus on the compounds' potential to be utilized as quality chemical biology probes.
References provided by Crossref.org
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