Pulse radiolysis studies of melatonin and chloromelatonin.

J Photochem Photobiol B

Fordham University, New York, NY 10023, USA.

Published: February 1998

AI Article Synopsis

  • The compounds melatonin and 6-chloromelatonin inhibit the growth of melanoma cells through possible redox reactions.
  • Studies using pulse radiolysis show that the reaction rates of these compounds with various radicals depend on their chemical structure.
  • Specifically, both compounds react quickly with hydroxyl radicals, but not with superoxide radicals.

Article Abstract

The endogenous indole melatonin and the melatonin receptor agonist 6-chloromelatonin block the proliferation of both dermal and uveal melanoma cells by mechanisms that may involve redox reactions. The interactions of hydrated electrons, the azide radical, hydroxyl radicals and superoxide with melatonin and its 6-chloro analogue have been studied using the technique of pulse radiolysis. The reaction rate constants of eaq- and N3 x with these compounds were found to be dependent on substitution at the sixth position. The rate constants for reaction of 6-chloromelatonin and melatonin with solvated electrons are 4.5 x 10(9) M-1 s-1 and 4.2 x 10(8) M-1 s-1, respectively. The reaction rate constants of N3 x with malatonin and chloromelatonin are 9.8 x 10(9) M-1 s-1 and 3.5 x 10(9) M-1 s-1 and 3.5 x 10(9) M-1 s-1, respectively. Melatonin and 6-chloromelatonin react with hydroxyl radicals at near diffusion controlled rates (1.3 x 10(10) M-1 s-1, 8.2 x 10(9) M-1 s-1). Melatonin and 6-chloromelatonin did not react with superoxide radicals and we calculate an upper limit of 1.0 x 10(4) M-1 s-1 for the rate constant for reaction of melatonin and 6-chloromelatonin with superoxide ion.

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http://dx.doi.org/10.1016/s1011-1344(97)00132-2DOI Listing

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