3-[5-(1H-Indol-3-ylmethylene)-4-oxo-2-thioxothiazolidin-3-yl]-propionic Acid as a Potential Polypharmacological Agent

Author:

Konechnyi Yulian1ORCID,Lozynskyi Andrii2,Ivasechko Iryna3,Dumych Tetiana3,Paryzhak Solomiya3,Hrushka Oksana4,Partyka Ulyana5,Pasichnyuk Iryna6,Khylyuk Dmytro7ORCID,Lesyk Roman2ORCID

Affiliation:

1. Department of Microbiology, Danylo Halytsky Lviv National Medical University, 69 Pekarska, 79010 Lviv, Ukraine

2. Department of Pharmaceutical, Organic and Bioorganic Chemistry, Danylo Halytsky Lviv National Medical University, 69 Pekarska, 79010 Lviv, Ukraine

3. Department of Regulation of Cell Proliferation and Apoptosis, Institute of Cell Biology, Position at the NAS of Ukraine, 79000 Lviv, Ukraine

4. Central Research Laboratory and Industrial Toxicology Laboratory, Danylo Halytsky Lviv National Medical University, Pekarska Str., 69 a, 79010 Lviv, Ukraine

5. Andrej Krypynsky Lviv Medical Academy, Department of Pharmacy, 79010 Lviv, Ukraine

6. Department of Pediatrics No.1, Medical Faculty, Danylo Halytsky Lviv National Medical University, 79010 Lviv, Ukraine

7. Department of Organic Chemistry, Faculty of Pharmacy, Medical University of Lublin, 4A Chodźki Street, 20-093 Lublin, Poland

Abstract

Searching for new types of biological activities among preliminarily identified hit compounds is a key challenge in modern medicinal chemistry. In our study, a previously studied 3-[5-(1H-indol-3-ylmethylene)-4-oxo-2-thioxothiazolidin-3-yl]-propionic acid (Les-6614) was screened for antimicrobial, antifungal, anti-allergic, and antitumor activities. Moreover, cytotoxicity, molecular docking, and SwissAdme online target screening were accomplished. It was determined that the Les-6614 has slight antimicrobial and antitumor activity. However, the studied compound decreased IgE levels in sensitized guinea pigs by 33–86% and reduced IgA, IgM, IL-2, and TNF-α, indicating anti-inflammatory and anti-allergic aactivities. According to the SwissADME web tool, target predictions for Les-6614 potentially have an affinity for lysosomal protective protein, Thromboxane-A synthase, and PPARγ. The molecular docking confirmed that the studied 2-thioxo-4-thiazolidinone derivative showed good bonding with LLP and TXAS, leading to stable protein–ligand complexes. Additionally, Les-6614 is a potential PPARγ modulator, which is important in the pathogenesis of allergy, cancer, and cardiovascular diseases.

Funder

Ministry of Health of Ukraine

National Research Foundation of Ukraine

Publisher

MDPI AG

Subject

Pharmaceutical Science

Reference36 articles.

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