氨基酸合成及氨基酸前药的抗肿瘤活性。

Anti-cancer drug design Pub Date : 1999-12-01
K Ohsumi, T Hatanaka, R Nakagawa, Y Fukuda, Y Morinaga, Y Suga, Y Nihei, K Ohishi, Y Akiyama, T Tsuji
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引用次数: 0

摘要

本文报道了水溶性氨基酸前药氨基酸的合成及其抗肿瘤活性。在合成的化合物中,7e (CS-39-L-Ser HCI, AC-7700)在结肠癌小鼠腺癌模型中表现出增强的抗肿瘤活性和降低的毒性。化合物7e具有较好的溶解度,易于配制为体内给药。化合物7e在小鼠和人的全血中被裂解生成母体化合物CS-39,可能是通过红细胞膜上的氨基肽酶的作用。
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Synthesis and antitumor activities of amino acid prodrugs of amino-combretastatins.

The synthesis and antitumor activity of water-soluble amino acid prodrugs of amino-combretastatins were reported. Among the synthesized compounds, 7e (CS-39-L-Ser HCI, AC-7700) showed enhanced antitumor activity and decreased toxicity in a Colon 26 murine adenocarcinoma model. Compound 7e showed improved solubility and was easily formulated for in vivo administration. Compound 7e was cleaved to generate the parent compound, CS-39, in the whole blood of mice as well as man, possibly by the action of amino peptidase on the erythrocyte membrane.

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