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首页> 外文期刊>Journal of Medicinal Chemistry >Design and Synthesis of Norendoxifen Analogues with Dual Aromatase Inhibitory and Estrogen Receptor Modulatory Activities
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Design and Synthesis of Norendoxifen Analogues with Dual Aromatase Inhibitory and Estrogen Receptor Modulatory Activities

机译:具有双重芳香酶抑制和雌激素受体调节活性的诺伦多芬类似物的设计与合成

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摘要

Both selective estrogen receptor modulators and aromatase inhibitors are widely used for the treatment of breast cancer. Compounds with both aromatase inhibitory and estrogen receptor modulatory activities could have special advantages for treatment of breast cancer. Our previous efforts led to the discovery of norendoxifen as the first compound with dual aromatase inhibitory and estrogen receptor binding activities. To optimize its efficacy and aromatase selectivity versus other cytochrome P450 enzyme, a series of structurally related norendoxifen analogues were designed and synthesized. The most potent compound, 4'-hydroxynorendoxifen (10), displayed elevated inhibitory potency against aromatase and enhanced affinity for estrogen receptors when compared to norendoxifen. The selectivity of 10 for aromatase versus other cytochrome P450 eniymes was also superior to norendoxifen. 4'-Hydroxynorendoxifen is therefore an interesting lead for further development to obtain new anticancer agents of potential value for the treatment of breast cancer.
机译:选择性雌激素受体调节剂和芳香酶抑制剂均被广泛用于乳腺癌的治疗。具有芳香酶抑制作用和雌激素受体调节作用的化合物可能具有治疗乳腺癌的特殊优势。我们先前的努力导致了去甲诺昔芬作为第一种具有双重芳香酶抑制和雌激素受体结合活性的化合物的发现。为了优化其功效和相对于其他细胞色素P450酶的芳香酶选择性,设计并合成了一系列结构相关的降氧芬净类似物。最有效的化合物4'-hydroxynorendoxifen(10)与norendoxifen相比,对芳香化酶的抑制作用增强,对雌激素受体的亲和力增强。相对于其他细胞色素P450酶,芳香酶的选择性为10,也优于去甲多昔芬。因此,4'-羟基去氧诺昔芬是进一步发展的有趣的线索,以获得具有潜在价值的新的抗癌药,可用于治疗乳腺癌。

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