| Literature DB >> 3343982 |
H Morita1, M Umeda, T Masuda, Y Ueno.
Abstract
Employing a suspension culture of a mouse mammary carcinoma cell line, FM3A cells, the cytotoxicity and induced mutagenicity of emodin (EM) were examined and compared with those of 2-hydroxy-emodin (2-OH-EM), which was identified as an active form of EM in the Ames/microsomes assay. EM was cytotoxic to FM3A cells in concentrations of 1-10 micrograms/ml, and induced 6-thioguanine-resistant (6TGr) mutation. 2-OH-EM was a little more toxic than EM, but induced little mutation.Entities:
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Year: 1988 PMID: 3343982 DOI: 10.1016/0165-1218(88)90107-3
Source DB: PubMed Journal: Mutat Res ISSN: 0027-5107 Impact factor: 2.433