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从 Piper truncatum 中分离出的木脂素类化合物作为新型有效的抗锥虫化合物。

Lignans Isolated from Piper truncatum Act as New Potent Antitrypanosomal Compounds.

机构信息

Center for Natural and Human Sciences, Federal University of ABC, 09210-580, Santo Andre, SP, Brazil.

Butantan Institute, 05503-900, 1500, São Paulo, SP, Brazil.

出版信息

Chem Biodivers. 2024 May;21(5):e202400547. doi: 10.1002/cbdv.202400547. Epub 2024 Apr 12.

DOI:10.1002/cbdv.202400547
PMID:38507773
Abstract

The hexane extract from twigs of Piper truncatum Vell (Piperaceae) displayed activity against Trypanosoma cruzi and was subjected to chromatographic steps to afford six dibenzylbutyrolactolic lignans, being four knowns: cubebin (1), (-)-9α-O-methylcubebin (2), (+)-9β-O-methylcubebinin (3) and 3,4-dimethoxy-3,4-demethylenedioxycubebin (4) as well as two new, named truncatin A (5) and B (6). Initially, in vitro activity against trypomastigotes was evaluated and compounds 1, 4 and 6 exhibited EC values of 41.6, 21.0 and 39.6 μM, respectively. However, when tested against amastigotes, the relevant clinical form in the chronic phase of Chagas disease, compounds 1-6 displayed activities with EC values ranging from 1.6 to 13.7 μM. In addition, the mammalian cytotoxicity of compounds 1-6 was evaluated against murine fibroblasts (NCTC). Compounds 2, 3 and 4 exhibited reduced toxicity against NCTC cells (CC>200 μM), resulting in SI values of>21.9,>14.5 and>121.9, respectively. Compound 4 showed the highest potency with an SI value twice superior to that determined by the standard drug benznidazole (SI>54.6) against the intracellular amastigotes. These data suggest that lignan 4 can be considered a possible scaffold for designing a new drug candidate for Chagas disease.

摘要

荜澄茄小枝的正己烷提取物(胡椒科)对克氏锥虫表现出活性,并经过色谱步骤得到六个二苄基丁内酯木脂素,其中四个为已知物:荜澄茄素(1)、(-)-9α-O-甲基荜澄茄素(2)、(+)-9β-O-甲基荜澄茄宁(3)和 3,4-二甲氧基-3,4-亚甲二氧基荜澄茄素(4)以及两个新化合物,命名为 truncatin A(5)和 B(6)。最初,评估了对锥虫体的体外活性,化合物 1、4 和 6 的 EC 值分别为 41.6、21.0 和 39.6 μM。然而,当测试对抗阿米巴原虫时,即恰加斯病慢性期的相关临床形式,化合物 1-6 的活性 EC 值范围为 1.6 至 13.7 μM。此外,还评估了化合物 1-6 对小鼠成纤维细胞(NCTC)的哺乳动物细胞毒性。化合物 2、3 和 4 对 NCTC 细胞的毒性降低(CC>200 μM),导致 SI 值分别为>21.9、>14.5 和>121.9。化合物 4 显示出最高的效力,其 SI 值是标准药物苯并咪唑(SI>54.6)对细胞内阿米巴原虫活性的两倍。这些数据表明木脂素 4 可被认为是设计治疗恰加斯病新药的潜在支架。

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