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Kinase Inhibitor Indole Derivatives as Anticancer Agents: A Patent Review

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F17%3A73584882" target="_blank" >RIV/61989592:15310/17:73584882 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.2174/1574892811666161003112119" target="_blank" >http://dx.doi.org/10.2174/1574892811666161003112119</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2174/1574892811666161003112119" target="_blank" >10.2174/1574892811666161003112119</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Kinase Inhibitor Indole Derivatives as Anticancer Agents: A Patent Review

  • Original language description

    Cancer accounts for a number of deaths each year. Consequently, prevention of this deadly disease is more challenging and hence the invention of new anticancer agents is of utmost importance. The current review elaborates the importance of indole designs as patented in the form of anticancer drug-like molecules targeting different cites of biological arena. Specific attention was given to kinases such as platelet-derived growth factor receptor, vascular endothelial growth factor receptor and fibroblast growth factor receptor, Bruton&apos;s tyrosine kinase, anaplastic lymphoma kinase, Janus kinase, cyclin-dependent kinase aurora kinases A, B and C, checkpoint kinases, protein kinase R, Pim kinases, phosphoinositide 3kinase, altered proteins kinases, polo-like kinase and many more. Moreover, the article summarizes the mode of action through the particular functions of kinases and the inhibitory potential of indole derivatives toward specific kinase. Certain patents gathered in the existing review article suggest that indole core can be a versatile foundation to discover drug-like kinase inhibitor molecules and modification of substituents existing on the indole moiety may have important impact on the pharmacokinetic and pharmacodynamics aspects of the resultant scaffolds. The information presented here would gather a great deal of interest to identify the new molecular designs bearing indole nucleus presenting novel anticancer drugs with a wide variety of biological targets involved in cancer pathology focusing on the inhibition of tyrosine kinases, serine/ threonine-specific protein kinases, cyclin-dependent kinases, lipid kinases and altered protein kinases.

  • 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

    10403 - Physical chemistry

Result continuities

  • Project

    <a href="/en/project/LM2015073" target="_blank" >LM2015073: Nanomaterials and Nanotechnologies for Environment Protection and Sustainable Future</a><br>

  • Continuities

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

Others

  • Publication year

    2017

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Recent Patents on Anti-Cancer Drug Discovery

  • ISSN

    1574-8928

  • e-ISSN

  • Volume of the periodical

    12

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    AE - UNITED ARAB EMIRATES

  • Number of pages

    18

  • Pages from-to

    55-72

  • UT code for WoS article

    000397249100006

  • EID of the result in the Scopus database

    2-s2.0-85011015033