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IUPAC name acetic acid | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ECHA InfoCard | 100.222.821 |
PubChem CID | |
CompTox Dashboard (EPA) | |
SMILES
| |
Properties | |
Chemical formula | C23H22ClNO2 |
Molar mass | 379.879 g·mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
Licofelone is a dual COX/LOX inhibitor being considered as a treatment for osteoarthritis and which is under development by Merckle GmbH with partners Alfa Wassermann and Lacer.
Licofelone is both an analgesic and an anti-inflammatory. Inhibition of 5-LOX may reduce the gastrointestinal toxicity associated with other non-steroidal anti-inflammatory drugs, which only inhibit COX (cyclooxygenase). Licofelone is the first drug to inhibit both. It has passed the phase III trials.
References
- Fischer L; Hornig M; Pergola C; et al. (2007). "The molecular mechanism of the inhibition by licofelone of the biosynthesis of 5-lipoxygenase products". British journal of pharmacology. 152 (4): 471–80. doi:10.1038/sj.bjp.0707416. PMC 2050828. PMID 17704828.
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ignored (help) - Vidal C; Gómez-Hernández A; Sánchez-Galán E; et al. (2007). "Licofelone, a balanced inhibitor of cyclooxygenase and 5-lipoxygenase, reduces inflammation in a rabbit model of atherosclerosis". The Journal of pharmacology and experimental therapeutics. 320 (1): 108–16. doi:10.1124/jpet.106.110361. PMID 17015640.
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ignored (help) - Alvaro-Gracia JM (2004). "Licofelone--clinical update on a novel LOX/COX inhibitor for the treatment of osteoarthritis". Rheumatology (Oxford, England). 43 Suppl 1: i21–5. doi:10.1093/rheumatology/keh105. PMID 14752172.
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ignored (help) - http://www.drugdevelopment-technology.com/projects/licofelone/
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