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Title: Radioprotection of EMT6 tumor by a new class of radioprotectors based on a pseudo-peptide cysteamine combination. Author: Lespinasse F, Oiry J, Fatome M, Ardouin P, Imbach J, Malaise EP, Guichard M. Journal: Int J Radiat Oncol Biol Phys; 1985 May; 11(5):1035-8. PubMed ID: 2985525. Abstract: Although WR-2721 preferentially protects normal tissues against irradiation, it seemed desirable to find other drugs presenting a lower toxicity and the same radioprotective properties. A new compound, I 102, was selected; it was characterized on one hand by a coupling between cysteamine and an amino-acid, and on the other hand by an acetyl-group, which protects the thiol function. The effects of WR-2721 and of I 102 were studied on EMT6 tumors grafted on BALB/c mice. Whatever the size of the tumor, the cell survival increased as a function of the time elapsed between the injection of I 102 and the end of the irradiation (TI). In contrast, the radioprotection afforded by WR-2721 was found to be independent of TI. The survival curves suggest that, like WR-2721, I 102 protects essentially oxygenated cells.[Abstract] [Full Text] [Related] [New Search]