- In vitro and ex vivo free radical scavenging activities of carazostatin, carbazomycin B and their derivatives
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Free radical scavenging activities of various carbazole compounds, carazostatin, carbazomycin B and their chemically modified derivatives were studied in vitro and ex vivo. Among these compounds, carazostatin, which was isolated as a free radical scavenger from the culture of Streptomyces chromofuscus, showed the most potent inhibitory activity against lipid peroxidation of rat brain homogenate in vitro. Carbazomycin B, a known antimicrobial antibiotic, also exhibited strong activity in this system. Although O-modified derivatives of carazostatin and carbazomycin B retained considerable activity, N,O-dimethyl derivatives did not suppress the peroxidation. On the other hand, the results from the ex vivo evaluation of these carbazoles in the lipid peroxidation system of mouse blood plasma showed that the original compounds as well as their O-modified derivatives had a strong inhibitory activity upon oral administration to mice. These findings suggest that these natural carbazoles and their effective derivatives can protect tissues from the peroxidative damage due to generation of free radicals.
- Kato,Kawasaki,Urata,Mochizuki
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- Synthesis and Electrochemical Properties of the Naturally Occuring Free Radical Scavenger Carazostatin
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A short synthesis of the naturally occuring free radical scavenger carazostatin 1 starting from indol-3-ylacetic acid is described, the key step being the regiospecific Diels-Alder reaction of the indolopyrone 2 with ethyl trimethylsilylpropynoate.Electro
- Jackson, P. Mark,Moody, Christopher J.,Mortimer, Roger J.
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p. 2941 - 2944
(2007/10/02)
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