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Synthesis, Anti-Tumor and Anti-Angiogenic Activity Evaluations of Asiatic Acid Amino Acid Derivatives

机译:亚洲氨基酸衍生物的合成,抗肿瘤和抗血管生成活性的评价

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Fifteen semi-synthetic derivatives of asiatic acid (AA) have been synthesized and evaluated for their biological activities. The successful modification of these compounds at the C-2, C-3, C-23 and C-28 positions was confirmed using NMR, MS and IR spectra. Further, their anti-tumor effects were evaluated in vitro using different cancer cell lines (HeLa, HepG2, B16F10, SGC7901, A549, MCF7 and PC3), while their anti-angiogenic activities were evaluated in vivo using a larval zebrafish model. Among the derivatives, compounds 4-10 showed more potent cytotoxic and anti-angiogenic effects than AA, while compounds 11-17 had significantly less effects. The new derivative 10 was also included in finished formulations to evaluate its stability using HPLC due to its potential topical use. The derivative 10 had markedly better anti-tumor activities than both AA and other derivatives, with similar stability as its parent compound AA.
机译:已经合成了十五种亚硫酸(AA)的半合成衍生物,并对其生物学活性进行了评估。使用NMR,MS和IR光谱证实了这些化合物在C-2,C-3,C-23和C-28位置的成功修饰。此外,使用不同的癌细胞系(HeLa,HepG2,B16F10,SGC7901,A549,MCF7和PC3)在体​​外评估了它们的抗肿瘤作用,同时使用幼虫斑马鱼模型在体内评估了它们的抗血管生成活性。在衍生物中,化合物4-10显示出比AA更有效的细胞毒性和抗血管生成作用,而化合物11-17则显示出明显更低的作用。由于其潜在的局部用途,新的衍生物10也包含在最终制剂中,以评估使用HPLC的稳定性。衍生物10具有比AA和其他衍生物明显更好的抗肿瘤活性,并且具有与其母体化合物AA相似的稳定性。

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