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Tolfenamic acid


Tolfenamic acid


Tolfenamic acid (Clotam, Tufnil, TFA) is a member of the anthranilic acid derivatives (or fenamate) class of NSAID drugs. Like other members of the class, it is a COX inhibitor and prevents formation of prostaglandins.

It is used in the UK as a treatment for migraine. It is generally not available in the US. It is available in some Asian, Latin American and European countries as a generic drug for humans and for animals.

Medical uses

TFA, like other non-steroidal anti-inflammatory drugs (NSAIDs), finds utility in the prevention and treatment of conditions associated with pain and inflammation. However, despite its efficacy when administered intramuscularly, subcutaneously, or orally, TFA-based drugs have not yet gained approval in the United States and some other countries due to the significant number of reported side effects.

Nevertheless, TFA exhibits promise in medical practice, demonstrating the ability to inhibit the growth of cancer cells in the pancreas, sigmoid colon, and rectum. Further research and development may unveil its potential for therapeutic applications in the future.

Chemistry

Tolfenamic acid, belonging to the pharmacological group of fenamates, possesses a chemical structure typical of anthranilic acid derivatives. In this structure, one of the hydrogen atoms of the nitro group is substituted by a benzene ring featuring a methyl group and a chlorine atom at the ortho- and meta- positions, respectively.

Currently, nine forms of TFA have been identified, some of which are determined by conformational states. These polymorphic forms exhibit variations in the spatial arrangement within the unit cell and in the values of the C-N(H)-C-C angle. This diversity in solid forms makes TFA an attractive candidate for modification and utilization in medical applications.

History

It was discovered by scientists at Medica Pharmaceutical Company in Finland.

References

External links

  • Tolfenamic acid information (Diseases Database)
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Text submitted to CC-BY-SA license. Source: Tolfenamic acid by Wikipedia (Historical)