Paper
In vitro and in vivo inhibitory activity of 6-amino-2,4,5-trimethylpyridin-3-ols against inflammatory bowel disease.
Published Oct 1, 2016 · S. Banskota, Han-eol Kang, Dong-Guk Kim
Bioorganic & medicinal chemistry letters
Q2 SJR score
15
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
6-amino-2,4,5-trimethylpyridin-3-ols show potential as a novel platform for anti-inflammatory bowel disease drug discovery, with compound 8m showing over 300-fold better efficacy than sulfasalazine in a rat model of colitis.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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References
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BJ-1108, a 6-Amino-2,4,5-Trimethylpyridin-3-ol Analog, Inhibits Serotonin-Induced Angiogenesis and Tumor Growth through PI3K/NOX Pathway
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Citations
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2024·1citation·B. Awasthi et al.·Journal of medicinal chemistry
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Synthesis of Pyridoxine-Derived Dimethylpyridinols Fused with Aminooxazole, Aminoimidazole, and Aminopyrrole
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2021·1citation·S. V. Fedoseev et al.·Synthetic Communications
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Compound 2-19 shows potential as a dual-acting IBD drug, targeting both TNF- and IL-6 signaling, and shows better anticolitis activity than compound 1 and sulfasalazine.
2021·8citations·Ujjwala Karmacharya et al.·Bioorganic & medicinal chemistry letters
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Synthesis and anti-hepatocellular carcinoma activity of aminopyridinol–sorafenib hybrids
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2021·3citations·B. Awasthi et al.·Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry