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PTP1B inhibitory and cytotoxic activities of triterpenoids from the aerial parts of Agrimonia pilosa

机译:来自Agrimonia Pilosa的航拍的三萜类化合物的PTP1B抑制和细胞毒性活性

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摘要

Recently, PTP1B inhibitors have become the frontier as possible targeting for anti-cancer and anti-diabetic drugs. Twelve triterpenoids from the aerial parts of Agrimonia pilosa were investigated for PTP1B inhibitory and cytotoxic activities. In the results, compounds 3 (IC50 = 0.50 mu M) and 7 (IC50 = 5.88 mu M) were found to possess very powerful inhibitory activity against the PTP1B enzyme, comparable to the positive control ursolic acid (IC50 = 6.60 mu M). In addition, compounds 1, 2, 4, and 10-12 showed potent inhibitory effects against PTP1B, with an IC50 range of 13.48aEuro'14.98 mu M. In the kinetic assay of the PTP1B enzyme, compounds 1 and 2 were noncompetitive, whereas 7 and 11 showed a mixed type. In the docking analysis, the results showed that different residues of PTP1B interacted with twelve triterpenoids. Furthermore, compounds 6 (IC50 = 3.65 mu M) and 12 (IC50 = 1.21 mu M) displayed strong cytotoxic effects against the HeLa cell line. Compounds 2 (IC50 = 16.06 mu M) and 4 (IC50 = 14.73 mu M) showed moderate cytotoxic activities against the HeLa cell line. Compound 2 exhibited comprehensive cytotoxicity against the HL-60 (IC50 = 45.53 mu M) and MCF-7 (IC50 = 34.21 mu M) cell lines. These results support the use of triterpenoids in traditional medicine for prevention and treatment of diabetes and cancer.
机译:最近,PTP1B抑制剂尽可能成为抗癌和抗糖尿病药物可能的靶向前沿。从Agrimonia pilosa的空中零部件进行了1​​2个Triterpenoids进行PTP1B抑制和细胞毒性活动。在结果中,发现化合物3(IC50 =0.50μm)和7(IC50 =5.88μm)对PTP1B酶具有非常强大的抑制活性,与阳性对照熊酸(IC50 =6.60μm)相当。此外,化合物1,2,4和10-12对PTP1B表示有效的抑制作用,IC50范围为13.48Aeuro'14.98μm。在PTP1B酶的动力学测定中,化合物1和2是非竞争力的,而图7和11显示了混合类型。在对接分析中,结果表明,PTP1b的不同残留物与12个三萜类化合物相互作用。此外,化合物6(IC50 =3.65μm)和12(IC50 =1.21μm)显示对HeLa细胞系的强细胞毒性作用。化合物2(IC50 =16.06μm)和4(IC50 =14.73μm)显示对Hela细胞系的中度细胞毒性活性。化合物2对HL-60(IC50 =45.53μm)和MCF-7(IC50 =34.21μm)细胞系具有综合细胞毒性。这些结果支持使用Triterpenoids在传统医学中用于预防和治疗糖尿病和癌症。

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