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2,3-吲哚桦木酸及其甘氨酸缀合物的体外抗黑色素瘤和抗菌活性比较

Comparison of In Vitro Antimelanoma and Antimicrobial Activity of 2,3-Indolo-betulinic Acid and Its Glycine Conjugates.

作者信息

Lombrea Adelina, Semenescu Alexandra-Denisa, Magyari-Pavel Ioana Zinuca, Turks Māris, Lugiņina Jevgeņija, Peipiņš Uldis, Muntean Delia, Dehelean Cristina Adriana, Dinu Stefania, Danciu Corina

机构信息

Department of Pharmacognosy, "Victor Babes" University of Medicine and Pharmacy Timisoara, Eftimie Murgu Square, No. 2, 300041 Timisoara, Romania.

Research Center for Pharmaco-Toxicological Evaluation, "Victor Babes" University of Medicine and Pharmacy Timisoara, Eftimie Murgu Square, No. 2, 300041 Timisoara, Romania.

出版信息

Plants (Basel). 2023 Mar 9;12(6):1253. doi: 10.3390/plants12061253.

Abstract

Malignant melanoma is one of the most pressing problems in the developing world. New therapeutic agents that might be effective in treating malignancies that have developed resistance to conventional medications are urgently required. Semisynthesis is an essential method for improving the biological activity and the therapeutic efficacy of natural product precursors. Semisynthetic derivatives of natural compounds are valuable sources of new drug candidates with a variety of pharmacological actions, including anticancer ones. Two novel semisynthetic derivatives of betulinic acid-N-(2,3-indolo-betulinoyl)diglycylglycine (BA1) and N-(2,3-indolo-betulinoyl)glycylglycine (BA2)-were designed and their antiproliferative, cytotoxic, and anti-migratory activity against A375 human melanoma cells was determined in comparison with known N-(2,3-indolo-betulinoyl)glycine (BA3), 2,3-indolo-betulinic acid (BA4) and naturally occurring betulinic acid (BI). A dose-dependent antiproliferative effect with IC values that ranged from 5.7 to 19.6 µM was observed in the series of all five compounds including betulinic acid. The novel compounds BA1 (IC = 5.7 µM) and BA2 (IC = 10.0 µM) were three times and two times more active than the parent cyclic structure B4 and natural BI. Additionally, compounds BA2, BA3, and BA4 possess antibacterial activity against ATCC 19615 and ATCC 25923 with MIC values in the range of 13-16 µg/mL and 26-32 µg/mL, respectively. On the other hand, antifungal activity toward ATCC 10231 and ATCC 22019 was found for compound BA3 with MIC 29 µg/mL. This is the first report of antibacterial and antifungal activity of 2,3-indolo-betulinic acid derivatives and also the first extended report on their anti-melanoma activity, which among others includes data on anti-migratory activity and shows the significance of amino acid side chain on the observed activity. The obtained data justify further research on the anti-melanoma and antimicrobial activity of 2,3-indolo-betulinic acid derivatives.

摘要

恶性黑色素瘤是发展中国家面临的最紧迫问题之一。迫切需要可能有效治疗对传统药物产生耐药性的恶性肿瘤的新型治疗药物。半合成是提高天然产物前体生物活性和治疗效果的重要方法。天然化合物的半合成衍生物是具有多种药理作用(包括抗癌作用)的新药候选物的宝贵来源。设计了桦木酸的两种新型半合成衍生物——N-(2,3-吲哚-桦木酰基)二甘氨酰甘氨酸(BA1)和N-(2,3-吲哚-桦木酰基)甘氨酰甘氨酸(BA2),并与已知的N-(2,3-吲哚-桦木酰基)甘氨酸(BA3)、2,3-吲哚-桦木酸(BA4)和天然存在的桦木酸(BI)相比,测定了它们对A375人黑色素瘤细胞的抗增殖、细胞毒性和抗迁移活性。在包括桦木酸在内的所有五种化合物系列中均观察到剂量依赖性抗增殖作用,IC值范围为5.7至19.6 μM。新型化合物BA1(IC = 5.7 μM)和BA2(IC = 10.0 μM)的活性分别比母体环状结构B4和天然BI高三倍和两倍。此外,化合物BA2、BA3和BA4对ATCC 19615和ATCC 25923具有抗菌活性,MIC值分别在13 - 16 μg/mL和26 - 32 μg/mL范围内。另一方面,发现化合物BA3对ATCC 10231和ATCC 22019具有抗真菌活性,MIC为29 μg/mL。这是2,3-吲哚-桦木酸衍生物抗菌和抗真菌活性的首次报道,也是关于其抗黑色素瘤活性的首次扩展报道,其中包括抗迁移活性数据,并显示了氨基酸侧链对观察到的活性的重要性。所获得的数据证明了对2,3-吲哚-桦木酸衍生物的抗黑色素瘤和抗菌活性进行进一步研究的合理性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c583/10058300/85360ac87d1e/plants-12-01253-g001.jpg

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