Literature DB >> 17894645

Nitroparacetamol (NCX-701) and pain: first in a series of novel analgesics.

E Alfonso Romero-Sandoval1, M Mar Curros-Criado, Gema Gaitan, Carlos Molina, Juan F Herrero.   

Abstract

The combination of numerous classic drugs with nitric oxide donors has led to the development of new compounds with promising therapeutic activities in a great variety of situations, including cardiovascular and respiratory systems, ocular pressure, inflammation, and pain. One of the first compounds developed was NCX-701 or nitroparacetamol, resulting from the combination of paracetamol, a classic and popular analgesic used in a great number of over-the-counter medications because of its antipyretic and analgesic properties, and a nitrooxybutyroyl moiety, which releases nitric oxide at a low but steady level. Although paracetamol is devoid of most of the gastrointestinal toxicity associated with aspirin-like drugs, this type of compounds was first designed to take advantage of the cytoprotective properties of nitric oxide when released at low concentrations. However, the combination of these molecules also resulted in an unexpected enhancement of the analgesic activity of paracetamol. In fact, NCX-701 has been shown to be effective in acute nociception as well as in neuropathic pain, situations in which paracetamol and other COX inhibitors are devoid of any effect. In addition, NCX-701 is more potent and, in some circumstances, more effective than its parent compound in different models of inflammatory pain. Furthermore, whereas paracetamol lacks any effective antiinflammatory action, NCX-701 might reduce inflammation. All these results taken together imply that the mechanism of action of NCX-701 is different from that of paracetamol, although it is not yet established for either molecule. NCX-701 appears to be a promising compound in the treatment of different types of pain, with a likely better profile of side effects than its parent molecule, paracetamol. Although recent clinical trials provided data consistent with the preclinical profile of NCX-701, further studies are needed to support its clinical use.

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Year:  2007        PMID: 17894645      PMCID: PMC6494127          DOI: 10.1111/j.1527-3458.2007.00016.x

Source DB:  PubMed          Journal:  CNS Drug Rev        ISSN: 1080-563X


  4 in total

1.  The peripheral administration of a nitric oxide donor potentiates the local antinociceptive effects of a DOR agonist during chronic inflammatory pain in mice.

Authors:  Arnau Hervera; Sergi Leánez; Roger Negrete; Olga Pol
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2009-07-28       Impact factor: 3.000

Review 2.  The Contribution of Serotonergic Receptors and Nitric Oxide Systems in the Analgesic Effect of Acetaminophen: An Overview of the Last Decade.

Authors:  Yeşim Hamurtekin; Ammar Nouilati; Cansu Demirbatir; Emre Hamurtekin
Journal:  Turk J Pharm Sci       Date:  2020-02-19

3.  Local loperamide inhibits thermal hyperalgesia but not mechanical allodynia induced by intratibial inoculation of melanoma cells in mice.

Authors:  Verdad Curto-Reyes; Lucía Juárez; Eva García-Pérez; Manuel Florentino Fresno; Agustín Hidalgo; Luis Menéndez; Ana Baamonde
Journal:  Cell Mol Neurobiol       Date:  2008-03-22       Impact factor: 5.046

4.  Antinociceptive effects of NCX-701 (nitro-paracetamol) in neuropathic rats: enhancement of antinociception by co-administration with gabapentin.

Authors:  M Mar Curros-Criado; Juan F Herrero
Journal:  Br J Pharmacol       Date:  2009-07-23       Impact factor: 8.739

  4 in total

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