Synthesis of new 1-phenyl-3-{4-[(2 E )-3-phenylprop-2-enoyl]phenyl}-thiourea and urea derivatives with anti-nociceptive activity
Bioorganic & Medicinal Chemistry, ISSN: 0968-0896, Vol: 16, Issue: 18, Page: 8526-8534
2008
- 55Citations
- 27Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations55
- Citation Indexes55
- 55
- CrossRef45
- Captures27
- Readers27
- 27
Article Description
Chalcones or 1,3-diaryl-2-propen-1-ones are known to be useful for treating pain, inflammation, and certain diseases although their uses have not been scientifically verified. Due to the limitations of opioid and NSAID therapy, there is a continuing search for new analgesics. A series of novel new 1-phenyl-3-{4-[(2 E )-3-phenylprop-2-enoyl]phenyl}-thiourea and urea derivatives were synthesized and evaluated against writhing test in mice, following the aromatic substitution pattern proposed by Topliss. The results of the preliminary bioassays indicate that compound 3 presents promising anti-nociceptive activity in acetic acid-, formalin-, and glutamate-induced pain in mice, compared with some well-known non-steroidal anti-inflammatory and analgesic drugs.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S096808960800730X; http://dx.doi.org/10.1016/j.bmc.2008.08.019; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=51449097508&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/18722128; https://linkinghub.elsevier.com/retrieve/pii/S096808960800730X; https://dx.doi.org/10.1016/j.bmc.2008.08.019
Elsevier BV
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