Copper naproxen

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Copper naproxen
File:Copper naproxen.jpg
Sample of copper naproxen in a glass vial
File:Copper naproxen.svg
Names
Other names
Copper(II) 6-methoxy-a-methyl-2-naphthaleneacetate
Identifiers
3D model (JSmol)
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  • InChI=1S/2C14H14O3.Cu/c2*1-9(14(15)16)10-3-4-12-8-13(17-2)6-5-11(12)7-10;/h2*3-9H,1-2H3,(H,15,16);/q;;+2/p-2/t2*9-;/m00./s1
    Key: GBARQYVMLWJLEP-NAWJVIAPSA-L
  • COc1cc2ccc(cc2cc1)[C@H](C)C(=O)[O-].COc1cc2ccc(cc2cc1)[C@H](C)C(=O)[O-].[Cu+2]
Properties
C28H26CuO6
Molar mass 522.056 g·mol−1
Appearance Green solid
Solubility Soluble in methanol, 1,4-dioxane,[1] DMSO, DMF[2]
Related compounds
Related compounds
Copper aspirinate
Copper ibuprofenate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Copper naproxen is a chemical complex of copper2+ chelated with the anti-inflammatory drug naproxen.[1] Copper complexes of NSAIDs like naproxen have been shown to have greater anti-inflammatory properties than the base drug.[3][2]

Copper naproxen can be found as a monohydrate, and it can form complexes with other organic molecules such as nicotinyl alcohol, 3-methylpyridine, and caffeine.[1][4][5]

Preparation

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Copper naproxen is prepared by reacting sodium naproxen with a copper(II) salt such as copper(II) sulfate.[1]

2 C14H13NaO3 + CuSO4 → C28H26CuO6 + Na2SO4

References

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