ORCID: https://orcid.org/0000-0001-8888-5373; Willems, Sabine
ORCID: https://orcid.org/0000-0002-9755-3394; Arp, Christopher J.
ORCID: https://orcid.org/0000-0002-5059-6178; Morstein, Johannes; Haake, Caleb T.; Merk, Daniel
ORCID: https://orcid.org/0000-0002-5359-8128 and Trauner, Dirk
ORCID: https://orcid.org/0000-0002-6782-6056
(2023):
Development of Light‐Activated LXR Agonists.
In: ChemMedChem, Vol. 18, No. 11
[PDF, 5MB]
Abstract
Activation of the oxysterol-sensing transcription factor liver X receptor (LXR) has been studied as a therapeutic strategy in metabolic diseases and cancer but is compromised by the side effects of LXR agonists. Local LXR activation in cancer treatment may offer an opportunity to overcome this issue suggesting potential uses of photopharmacology. We report the computer-aided development of photoswitchable LXR agonists based on the T0901317 scaffold, which is a known LXR agonist. Azologization and structure-guided structure-activity relationship evaluation enabled the design of an LXR agonist, which activated LXR with low micromolar potency in its light-induced (Z)-state and was inactive as (E)-isomer. This tool sensitized human lung cancer cells to chemotherapeutic treatment in a light-dependent manner supporting potential of locally activated LXR agonists as adjuvant cancer treatment.
Item Type: | Journal article |
---|---|
Faculties: | Chemistry and Pharmacy > Department of Pharmacy Chemistry and Pharmacy > Department of Chemistry |
Subjects: | 500 Science > 540 Chemistry |
URN: | urn:nbn:de:bvb:19-epub-108861-6 |
ISSN: | 1860-7179 |
Language: | English |
Item ID: | 108861 |
Date Deposited: | 21. Mar 2024, 12:20 |
Last Modified: | 21. Mar 2024, 12:20 |