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Cdc-Like Kinases (CLKs): Biology, Chemical Probes, and Therapeutic Potential
P. Martín Moyano, V. Němec, K. Paruch
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články, přehledy
Grantová podpora
CZ.02.1.01/0.0/0.0/16_025/0007381
European Structural and Investment Funds, Operational Programme Research, Development and Education
NLK
Directory of Open Access Journals
od 2000
Free Medical Journals
od 2000
Freely Accessible Science Journals
od 2000
PubMed Central
od 2007
Europe PubMed Central
od 2007
ProQuest Central
od 2000-03-01
Open Access Digital Library
od 2000-01-01
Open Access Digital Library
od 2007-01-01
Health & Medicine (ProQuest)
od 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
od 2000
PubMed
33066143
DOI
10.3390/ijms21207549
Knihovny.cz E-zdroje
- MeSH
- antitumorózní látky farmakologie terapeutické užití MeSH
- inhibitory proteinkinas farmakologie terapeutické užití MeSH
- karcinogeneze účinky léků metabolismus MeSH
- lidé MeSH
- protein-serin-threoninkinasy antagonisté a inhibitory chemie genetika metabolismus MeSH
- tyrosinkinasy antagonisté a inhibitory chemie genetika metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy 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.
Citace poskytuje Crossref.org
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