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Contemporary mTOR inhibitor scaffolds to diseases breakdown: A patent review (2015–2021)

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62690094%3A18470%2F22%3A50019214" target="_blank" >RIV/62690094:18470/22:50019214 - isvavai.cz</a>

  • Alternative codes found

    RIV/00179906:_____/22:10445942

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0223523422004007?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0223523422004007?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.ejmech.2022.114498" target="_blank" >10.1016/j.ejmech.2022.114498</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Contemporary mTOR inhibitor scaffolds to diseases breakdown: A patent review (2015–2021)

  • Original language description

    Mechanistic target of rapamycin (mTOR) is a highly conserved protein kinase acting as a central regulator of cell functions. The kinase forms two distinct mTOR complexes termed as mTORC1 and mTORC2. Dysregulation of mTOR activity is associated with various pathological conditions. Inhibition of overactivated mTOR represent a rational approach in the treatment of numerous human diseases. Rapamycin is a potent natural inhibitor of mTOR exhibiting significant antitumor and immunosuppressive activity. Derivatization of rapamycin provided rapalogs, the first generation of mTOR inhibitors that selectively inhibit mTORC1 activity. Further interest of research community resulted in creation of the second generation of mTOR inhibitors involving both, mTOR kinase inhibitors and dual phosphoinositide 3-kinase (PI3K)/mTOR inhibitors. Recently, combining advances of first and second generation of mTOR inhibitors yielded in the third generation of inhibitors termed as rapalinks. Nowadays, novel inhibitors belonging to all of the three generations are still under development. These inhibitors help us better to understand role of mTOR in mTOR signaling pathway as well as in diverse human diseases. In this review, we summarize recent reported mTOR inhibitors or methods of use thereof in the treatment of various diseases. © 2022 Elsevier Masson SAS

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30107 - Medicinal chemistry

Result continuities

  • Project

    <a href="/en/project/GA20-22037S" target="_blank" >GA20-22037S: The therapeutic potential of novel mTOR inhibitors within the process of ageing</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2022

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    European Journal of Medicinal Chemistry

  • ISSN

    0223-5234

  • e-ISSN

    1768-3254

  • Volume of the periodical

    238

  • Issue of the periodical within the volume

    August

  • Country of publishing house

    FR - FRANCE

  • Number of pages

    29

  • Pages from-to

    "Article number: 114498"

  • UT code for WoS article

    000810543200004

  • EID of the result in the Scopus database

    2-s2.0-85131533377