Iboxamycin
Iboxamycin is a bioactive compound that belongs to the anthracycline family of antibiotics. It is known for its potent antitumor and antibacterial properties.
History[edit | edit source]
Iboxamycin was first isolated in the 1970s from the bacteria Streptomyces ibaraensis. Since then, it has been the subject of numerous pharmacological studies due to its potential therapeutic applications.
Structure and Properties[edit | edit source]
Iboxamycin is a tetracyclic compound with a characteristic anthracycline structure. It contains a quinone moiety and an amino sugar called daunosamine. The compound is highly lipophilic, which allows it to easily penetrate cell membranes.
Biological Activity[edit | edit source]
Iboxamycin exhibits strong antitumor activity by intercalating into DNA and inhibiting the enzyme topoisomerase II. This leads to DNA damage and cell death. The compound also shows antibacterial activity by inhibiting protein synthesis in bacteria.
Clinical Use[edit | edit source]
Despite its potent biological activity, the clinical use of iboxamycin is limited due to its high toxicity. However, research is ongoing to develop derivatives of iboxamycin with improved safety profiles.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD