Sulindac is a known anti-inflammatory drug that functions by inhibition of cyclooxygenases 1 and 2 (COX). There has been recent interest in Sulindac and other non-steroidal anti-inflammatory drugs (NSAID) because of their anti-tumor activity against colorectal cancer. Studies with sulindac have indicated that it may also function as an anti-tumor agent by stimulating apoptosis. Sulindac is a pro-drug, containing a methyl sulfoxide group, that must be reduced to sulindac sulfide to be active as a COX inhibitor. In the present studies we have developed a simple assay to measure sulindac reduction and tested sulindac as a substrate for 6 known members of the methionine sulfoxide reductase (Msr) family that have been identified in Escherichia coli. Only MsrA and a membrane associated Msr can reduce sulindac to the active sulfide. The reduction of sulindac also has been demonstrated in extracts of calf liver, kidney, and brain. Sulindac reductase activity is also present in mitochondria and microsomes.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.bbrc.2003.10.203 | DOI Listing |
J Colloid Interface Sci
February 2025
Tongji School of Pharmacy, Huazhong University of Science and Technology, Wuhan 430030, PR China. Electronic address:
Bioorg Med Chem
December 2024
Pharmaceutical Research Center and School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, PR China; Jiangsu Province Hi-Tech Key Laboratory for Biomedical Research, Southeast University, Nanjing 211189, PR China. Electronic address:
Cardiac inflammation, a pathological cornerstone in cardiac dysfunction, triggers diastolic impairment, leading to profound myocardial hypoxia. This hypoxic state serves as a potent stimulus for the amplification of inflammatory mediator release, ultimately limiting the therapeutic potential of monotherapies. To address this challenge, compounds that integrate non-steroidal anti-inflammatory drugs (NSAIDs) with nitric oxide (NO) donors was synthesized.
View Article and Find Full Text PDFNano Lett
November 2024
Department of Chemistry, Xihua University, Chengdu 610039, China.
Sulfoxides are essential in pharmaceuticals and chemicals, yet traditional thioether oxidation struggles with selectivity and sustainability. This study introduces carbonized polymer dots (CPDs) as effective photocatalysts for ecofriendly thioether to sulfoxide oxidation, using water and ethanol to enhance reaction selectivity and efficiency under 455 nm blue light. These catalysts not only show remarkable efficacy under mild conditions but also display high selectivity for sulfoxide formation, proving versatile across a broad range of substrates.
View Article and Find Full Text PDFMol Cancer
September 2024
Shengli Clinical Medical College of Fujian Medical University, Fuzhou, 350001, China.
The Nab-paclitaxel combined with gemcitabine (AG) regimen is the main chemotherapy regimen for pancreatic cancer, but drug resistance often occurs. Currently, the ability to promote sensitization in drug-resistant cases is an important clinical issue, and the strategy of repurposing conventional drugs is a promising strategy. This study aimed to identify a classic drug that targets chemotherapy resistance's core signaling pathways and combine it with the AG regimen to enhance chemosensitivity.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!