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Click Reactions in Chemistry of Triterpenes – Advances Towards Development of Potential Therapeutics

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F18%3A73591031" target="_blank" >RIV/61989592:15110/18:73591031 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15310/18:73591031

  • Result on the web

    <a href="http://dx.doi.org/10.2174/0929867324666171009122612" target="_blank" >http://dx.doi.org/10.2174/0929867324666171009122612</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2174/0929867324666171009122612" target="_blank" >10.2174/0929867324666171009122612</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Click Reactions in Chemistry of Triterpenes – Advances Towards Development of Potential Therapeutics

  • Original language description

    Triterpenoids are natural compounds with a large variety of biological activities such as anticancer, antiviral, antibacterial, antifungal, antiparazitic, antiinflammatory and others. Despite their low toxicity and simple availability from the natural resources, their clinical use is still severely limited by their higher IC50 and worse pharmacological properties than in the currently used therapeutics. This fact encouraged a number of researchers to develop new terpenic derivatives more suitable for the potential clinical use. This review summarizes a new approach to improve both, the activity and ADME-Tox properties by connecting active terpenes to another modifying molecules using click reactions. Within the past few years, this synthetic approach was well explored yielding a lot of great improvements of the parent compounds along with some less successful attempts. A large quantity of the new compounds presented here are superior in both activity and ADME-Tox properties to their parents. This review should serve the researchers who need to promote their hit triterpenic structures towards their clinical use and it is intended as a guide for the chemical synthesis of better drug candidates.

  • 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

    10401 - Organic chemistry

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

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

Others

  • Publication year

    2018

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    CURRENT MEDICINAL CHEMISTRY

  • ISSN

    0929-8673

  • e-ISSN

  • Volume of the periodical

    25

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    AE - UNITED ARAB EMIRATES

  • Number of pages

    23

  • Pages from-to

    636-658

  • UT code for WoS article

    000425888400006

  • EID of the result in the Scopus database

    2-s2.0-85043302943