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首页> 外文期刊>Molecules >Anti-Proliferative Activity of Triterpenoids and Sterols Isolated from Alstonia scholaris against Non-Small-Cell Lung Carcinoma Cells
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Anti-Proliferative Activity of Triterpenoids and Sterols Isolated from Alstonia scholaris against Non-Small-Cell Lung Carcinoma Cells

机译:来自Alstonia Scholaris与非小细胞肺癌细胞分离的三萜类化合物和甾醇的抗增殖活性

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摘要

(1) Background: In China and South Asia, Alstonia scholaris (Apocynaceae) is an important medicinal plant that has been historically used in traditional ethnopharmacy to treat infectious diseases. Although various pharmacological activities have been reported, the anti-lung cancer components of A. scholaris have not yet been identified. The objective of this study is to evaluate the active components of the leaf extract of A. scholaris, and assess the anti-proliferation effects of isolated compounds against non-small-cell lung carcinoma cells; (2) Methods: NMR was used to identify the chemical constitutes isolated from the leaf extract of A. scholaris. The anti-proliferative activity of compounds against non-small-cell lung carcinoma cells was assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay; (3) Results: Eight triterpenoids and five sterols were isolated from the hexane portion of A. scholaris, and structurally identified as: (1) ursolic acid, (2) oleanolic acid, (3) betulinic acid, (4) betulin, (5) 2,3,28-lup-20(29)-ene-triol, (6) lupeol, (7) -amyrin, (8) -amyrin, (9) poriferasterol, (10) epicampesterol, (11) -sitosterol, (12) 6-hydroxy-4-stigmasten-3-one, and (13) ergosta-7,22-diene-3,5,6-triol. Compound 5 was isolated from a plant source for the first time. In addition, compounds 9, 10, 12, and 13 were also isolated from A. scholaris for the first time. Ursolic acid, betulinic acid, betulin, and 2,3,28-lup-20(29)-ene-triol showed anti-proliferative activity against NSCLC, with IC50 of 39.8, 40.1, 240.5 and 172.6 M, respectively.; (4) Conclusion: These findings reflect that pentacyclic triterpenoids are the anti-lung cancer chemicals in A. scholaris. The ability of ursolic acid, betulinic acid, betulin, and 2,3,28-lup-20(29)-ene-triol to inhibit the proliferative activity of NSCLC can constitute a valuable group of therapeutic agents in the future.
机译:(1)背景:在中国和南亚,Alstonia Schararis(Apocynaceae)是一家重要的药用植物,历史上用于传统民族医生以治疗传染病。虽然已经报道了各种药理活动,但尚未确定A. Scholaris的抗肺癌成分。本研究的目的是评估A的叶子提取物的活性成分,并评估分离化合物对非小细胞肺癌细胞的抗扩散作用; (2)方法:NMR用于鉴定从A的叶子提取物中分离的化学构成物。用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑鎓溴化物(MTT)测定评估对非小细胞肺癌细胞的化合物的抗增殖活性; (3)结果:从A的己烷部分分离出八个三萜和五个甾醇,并在结构上鉴定为:(1)熊糖酸,(2)甲醛酸,(3)丁糖酸,(4)丁糖酸,( 5)2,3,28-LUP-20(29) - 三醇,(6)Lupeol,(7)-Amyrin,(8)-Myrin,(9)poriferasterol,(10)素食药物,(11) - Sitosterol,(12)6-羟基-4-stigmasten-3-one,和(13)ergosta-7,22-二烯-3,5,6-三醇。第一次从植物来源中分离化合物5。此外,第一次将化合物9,10,12和13分离出来。熊胆酸,桦木酸,桦木蛋白和2,3,28-LUP-20(29) - 三醇对NSCLC显示出抗增殖活性,分别为39.8,40.1,240.5和172.6米的IC50; (4)结论:这些发现反映了五胞苷三萜类化合物是A的抗肺癌化学品。熊果酸,桦木酸,桦木蛋白和2,3,28-LUP-20(29) - 三醇抑制NSCLC增殖活性的能力可以构成未来有价值的治疗剂。

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