Preclinical studies of PROTACs in hematological malignancies
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023736%3A_____%2F21%3A00013222" target="_blank" >RIV/00023736:_____/21:00013222 - isvavai.cz</a>
Result on the web
<a href="https://doi.org/10.2174/1871529X21666210308111546" target="_blank" >https://doi.org/10.2174/1871529X21666210308111546</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.2174/1871529X21666210308111546" target="_blank" >10.2174/1871529X21666210308111546</a>
Alternative languages
Result language
angličtina
Original language name
Preclinical studies of PROTACs in hematological malignancies
Original language description
Incorrectly expressed or mutated proteins associated with hematologic malignancies have been generally targeted by chemotherapy using small-molecule inhibitors or monoclonal antibodies. But the majority of these intracellular proteins are without active sites and antigens. PROTACs, proteolysis targeting chimeras, are bifunctional molecules designed to polyubiquitinate and degrade specific pathological proteins of interest (POIs) by hijacking the activity of E3-ubiquitin ligases for POI polyubiquitination and subsequent degradation by the proteasome.
Czech name
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Czech description
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Classification
Type
J<sub>SC</sub> - Article in a specialist periodical, which is included in the SCOPUS database
CEP classification
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OECD FORD branch
30205 - Hematology
Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2021
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Cardiovascular & hematological disorders drug targets
ISSN
1871-529X
e-ISSN
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Volume of the periodical
21
Issue of the periodical within the volume
1
Country of publishing house
AE - UNITED ARAB EMIRATES
Number of pages
16
Pages from-to
7-22
UT code for WoS article
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EID of the result in the Scopus database
2-s2.0-85115907360