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Design and synthesis of a siderophore conjugate as a potent PSMA inhibitor and potential diagnostic agent for prostate cancer

机译:铁载体结合物的设计和合成作为有效的PSMA抑制剂和潜在的前列腺癌诊断剂

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摘要

A Siderophore conjugate was designed as a potential PSMA inhibitor and diagnostic agent for prostate cancer. A semi-rigid spacer was incorporated to avoid competitive participation of iron binding by the enzyme inhibitor relative to the siderophore component. Biological test results showed that, even with the extended scaffold, this compound is a potent PSMA inhibitor with an IC50 of 4 nM. This siderophore conjugate may be useful for detection of prostate-derived cancer cells by magnetic resonance imaging (MRI).
机译:铁载体共轭被设计为潜在的PSMA抑制剂和前列腺癌的诊断剂。引入半刚性间隔基,以避免铁抑制剂相对于铁载体组分竞争性参与铁结合。生物学测试结果表明,即使使用扩展的支架,该化合物也是有效的PSMA抑制剂,IC50为4 nM。该铁载体共轭物可用于通过磁共振成像(MRI)检测前列腺来源的癌细胞。

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