Abstract
Two series of rhein analogues were synthesized with modification at the 3-position. Their cytotoxicities were evaluated using an MTT assay. Among all the compounds synthesized, one compound showed the best potency, with an IC(50) value of 2.7 μM against the HeLa cell line and 0.6 μM against the MOLT4 cell line.
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Anthraquinones / chemical synthesis
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Anthraquinones / chemistry*
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Anthraquinones / pharmacology
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Antineoplastic Agents / chemical synthesis
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Antineoplastic Agents / chemistry*
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Antineoplastic Agents / pharmacology
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Cell Line, Tumor
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Cell Proliferation / drug effects
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Humans
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Neoplasms
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Structure-Activity Relationship
Substances
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1,8-dihydroxy-3-(2'-chloro-acetamido)anthraquinone
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Anthraquinones
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Antineoplastic Agents
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rhein