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具有抗人黑色素瘤活性的桦木酸氨基酸缀合物的制备。

Preparation of amino acid conjugates of betulinic acid with activity against human melanoma.

作者信息

Jeong H J, Chai H B, Park S Y, Kim D S

机构信息

Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois at Chicago, 60612, USA.

出版信息

Bioorg Med Chem Lett. 1999 Apr 19;9(8):1201-4. doi: 10.1016/s0960-894x(99)00165-1.

Abstract

Betulinic acid has been coupled with a series of amino acids at C-28 carboxylic acid position and the toxicity of the derivatives has been evaluated against cultured human melanoma (MEL-2) and human epidermoid carcinoma of the mouth (KB) cell lines. A number of amino acid conjugates of betulinic acid showed improved water solubility as well as selective cytotoxicity. This investigation demonstrates that amino acid conjugates of betulinic acid can produce potentially important derivatives, which may be developed as antitumor agents.

摘要

桦木酸已在C-28羧酸位置与一系列氨基酸偶联,并评估了这些衍生物对培养的人黑素瘤(MEL-2)和人口腔表皮样癌(KB)细胞系的毒性。桦木酸的许多氨基酸缀合物显示出改善的水溶性以及选择性细胞毒性。这项研究表明,桦木酸的氨基酸缀合物可以产生潜在重要的衍生物,这些衍生物可能被开发为抗肿瘤药物。

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