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阿佐雷拉密苏里烷二萜类化合物的进一步研究。

Further mulinane diterpenoids from Azorella compacta.

机构信息

Departamento de Química, Facultad de Ciencias, Universidad de Chile, Casilla 653, Santiago, Chile.

出版信息

J Pharm Pharmacol. 2013 Aug;65(8):1231-8. doi: 10.1111/jphp.12083. Epub 2013 May 21.

Abstract

OBJECTIVES

The chemical study of a dichloromethane extract from Azorella compacta was directed to the isolation of characteristic mulinane and azorellane diterpenoids in order to determine their gastroprotective activity.

METHODS

Usual chromatographic techniques on the extract led to the isolation of 12 compounds, which were identified by their spectroscopic properties. The HCl/ethanol-induced gastric lesions model in mice was used to determine the gastroprotective activity.

KEY FINDINGS

The new diterpenoids, 13β-hydroxymulinane (1), mulin-11,13-dien-20-ol (2), 13α-methoxyazorellanol (3) and mulin-11,13-dien-18-acetoxy-16,20-dioic acid (12) were isolated from A. compacta. The known diterpenoids mulin-11,13-dien-20-oic acid (4), 13α-hydroxyazorellane (5), 13β-hydroxyazorellane (6), mulinic acid (7), mulinolic acid (8) and azorellanol (9), and the aromatic compounds 5,7-dihydroxychromone (10) and isoflavonoid biochanin A (11), were also obtained from the extract. Compounds 6, 9 and 12 at 20 mg/kg reduced gastric lesions by 69%, 71% and 73%, respectively, being statistically similar to lansoprazole at the same dose.

CONCLUSIONS

The results corroborate the intraspecific chemical variations detected previously in specimens of A. compacta collected at different Chilean latitudes. A high concentration of azorellanol (9) could account in part for some of the therapeutic properties attributed to this species, in particular in ulcer treatment. Most of the mulinane and azorellane diterpenoids isolated in this study showed relevant gastroprotective activity at a low dose in the bioassay.

摘要

目的

从密花远志中二氯甲烷提取物的化学成分研究,分离出具有特征性的木榴烷和远志烷二萜类化合物,以确定其胃保护活性。

方法

对提取物进行常规色谱技术处理,分离出 12 种化合物,通过光谱特性对其进行鉴定。采用盐酸/乙醇诱导的小鼠胃损伤模型来确定胃保护活性。

主要发现

从 A. compacta 中分离出新型二萜类化合物 13β-羟木榴烷(1)、木榴烷-11,13-二烯-20-醇(2)、13α-甲氧基远志醇(3)和木榴烷-11,13-二烯-18-乙酰氧基-16,20-二酸(12)。从提取物中还获得了已知的二萜类化合物木榴烷-11,13-二烯-20-酸(4)、13α-羟基远志烷(5)、13β-羟基远志烷(6)、木莲酸(7)、木莲醇酸(8)和远志醇(9),以及芳香族化合物 5,7-二羟基色酮(10)和异黄酮生物黄酮 A(11)。化合物 6、9 和 12 在 20 mg/kg 剂量下可分别减少 69%、71%和 73%的胃损伤,与相同剂量的兰索拉唑统计学上相似。

结论

结果证实了先前在不同智利纬度采集的 A. compacta 标本中检测到的种内化学变异。高浓度的远志醇(9)可能部分解释了该物种的一些治疗特性,特别是在治疗溃疡方面。本研究中分离出的大多数木榴烷和远志烷二萜类化合物在低剂量的生物测定中表现出显著的胃保护活性。

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