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Anti-Proliferative Activity of Triterpenoids and Sterols Isolated from Alstonia scholaris against Non-Small-Cell Lung Carcinoma Cells

机译:阿尔斯通氏菌分离的三萜和甾醇对非小细胞肺癌细胞的抗增殖活性

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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) 2β,3β,28-lup-20(29)-ene-triol, (>6) lupeol, (>7) β-amyrin, (>8) α-amyrin, (>9) poriferasterol, (>10) epicampesterol, (>11) β-sitosterol, (>12) 6β-hydroxy-4-stigmasten-3-one, and (>13) ergosta-7,22-diene-3β,5α,6β-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 2β,3β,28-lup-20(29)-ene-triol showed anti-proliferative activity against NSCLC, with IC50 of 39.8, 40.1, 240.5 and 172.6 μM, 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 2β,3β,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 Scholaris(Apocynaceae)是重要的药用植物,历史上一直在传统的民族药房中用于治疗传染病。尽管已经报道了各种药理活性,但尚未鉴定出A. Scholaris的抗肺癌成分。这项研究的目的是评估书生曲霉的叶提取物的活性成分,并评估分离的化合物对非小细胞肺癌细胞的抗增殖作用。 (2)方法:采用核磁共振法(NMR)鉴定从书生曲霉叶片提取物中分离出的化学成分。通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物(MTT)测定法评估化合物对非小细胞肺癌细胞的抗增殖活性; (3)结果:从A. Scholaris的己烷部分中分离出八种三萜和五种固醇,其结构鉴定为:(> 1 )乌索酸,(> 2 )齐墩果酸酸,(> 3 )桦木酸,(> 4 )桦木酸,(> 5 )2β,3β,28-lup-20(29)-烯-三醇,(> 6 )羽扇豆油,(> 7 )β-淀粉蛋白,(> 8 )α-淀粉蛋白,(> 9 < / strong>)卟啉甾醇,(> 10 )表甘醇,(> 11 )β-谷甾醇,(> 12 )6β-羟基-4-stigmasten- 3-one和(> 13 )麦角稳定剂7,22-二烯3β,5α,6β-三醇。化合物> 5 是首次从植物来源中分离出来的。此外,化合物A.studys的第一个化合物也分别是> 9 ,> 10 ,> 12 和> 13 。时间。熊果酸,桦木酸,桦木素和2β,3β,28-lup-20(29)-ene-triol对NSCLC均具有抗增殖活性,IC50分别为39.8、40.1、240.5和172.6μM。 (4)结论:这些发现反映了五环三萜类化合物是A. Scholaris中的抗肺癌化学物质。熊果酸,桦木酸,桦木素和2β,3β,28-lup-20(29)-ene-triol抑制NSCLC增殖活性的能力可在将来构成有价值的治疗药物。

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