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翠雀属生物碱及其对 HO 诱导的心肌细胞损伤的影响。

Alkaloids of Delphinium grandiflorum and their implication to HO-induced cardiomyocytes injury.

机构信息

Wuya College of Innovation, School of Traditional Chinese Materia Medica, Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.

Wuya College of Innovation, School of Traditional Chinese Materia Medica, Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.

出版信息

Bioorg Med Chem. 2021 May 1;37:116113. doi: 10.1016/j.bmc.2021.116113. Epub 2021 Mar 17.

Abstract

Three new diterpenoid alkaloids (1-3), and eight known alkaloids (4-11) were isolated from the aerial parts of Delphinium grandiflorum. Grandifline A (1) represents an unprecedented diterpenoid alkaloid ring system featuring a C-7NC17 hemiaminal moiety and a lactone fragment through the linkage of C-17OC19 unit. And we named this newly-discovered class of rearranged C-diterpenoid alkaloid scaffold as grandiflodines (B-12). Grandifline B (2) is the first naturally-occurring 7,17-secolycoctonine diterpenoid alkaloid with a C-7OC17 unit forming a hemiacetal. Their structures were elucidated via spectroscopic data and single-crystal X-ray diffraction analysis. The protective effects of compounds 1-11 on HO-induced cardiomyocytes injury were assayed. And compounds 6 and 10 showed significant protective effects, with IC values of 1.881 ± 0.680 μM and 1.904 ± 0.750 μM, respectively. Further, compound 6 could reduce oxidative damage by inhibiting cell death via the AMPK/AKT/mTOR signaling pathway in HO-induced H9C2 cells.

摘要

从翠雀属植物大花翠雀的地上部分分离得到三个新的二萜生物碱(1-3)和八个已知的生物碱(4-11)。大花灵碱 A(1)代表了一种前所未有的二萜生物碱环系统,其特征是通过 C-17OC19 单元的连接具有 C-7NC17 半亚胺和内酯片段。我们将这个新发现的重排 C-二萜生物碱支架类命名为大花灵碱(B-12)。大花灵碱 B(2)是第一个天然存在的具有 C-7OC17 单元形成半缩醛的 7,17-裂环海罂粟碱二萜生物碱。通过光谱数据和单晶 X 射线衍射分析阐明了它们的结构。测定了化合物 1-11 对 HO 诱导的心肌细胞损伤的保护作用。化合物 6 和 10 表现出显著的保护作用,IC 值分别为 1.881±0.680μM 和 1.904±0.750μM。此外,化合物 6 可以通过抑制 AMPK/AKT/mTOR 信号通路减少氧化损伤,从而抑制 HO 诱导的 H9C2 细胞中的细胞死亡。

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