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Targeting the pregnane X receptor using microbial metabolite mimicry

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F20%3A73601274" target="_blank" >RIV/61989592:15310/20:73601274 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.embopress.org/doi/full/10.15252/emmm.201911621" target="_blank" >https://www.embopress.org/doi/full/10.15252/emmm.201911621</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.15252/emmm.201911621" target="_blank" >10.15252/emmm.201911621</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Targeting the pregnane X receptor using microbial metabolite mimicry

  • Original language description

    The human PXR (pregnane X receptor), a master regulator of drug metabolism, has essential roles in intestinal homeostasis and abrogating inflammation. Existing PXR ligands have substantial off-target toxicity. Based on prior work that established microbial (indole) metabolites as PXR ligands, we proposed microbial metabolite mimicry as a novel strategy for drug discovery that allows exploiting previously unexplored parts of chemical space. Here, we report functionalized indole derivatives as first-in-class non-cytotoxic PXR agonists as a proof of concept for microbial metabolite mimicry. The lead compound, FKK6 (Felix Kopp Kortagere 6), binds directly to PXR protein in solution, induces PXR-specific target gene expression in cells, human organoids, and mice. FKK6 significantly represses pro-inflammatory cytokine production cells and abrogates inflammation in mice expressing the human PXR gene. The development of FKK6 demonstrates for the first time that microbial metabolite mimicry is a viable strategy for drug discovery and opens the door to underexploited regions of chemical space.

  • 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

    30104 - Pharmacology and pharmacy

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

    2020

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    EMBO Molecular Medicine

  • ISSN

    1757-4676

  • e-ISSN

  • Volume of the periodical

    12

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    19

  • Pages from-to

    "e11621-1"-"e11621-19"

  • UT code for WoS article

    000526640800009

  • EID of the result in the Scopus database

    2-s2.0-85081220801