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三萜类化合物对肺纤维化的防治作用。

Anti-Pulmonary Fibrosis Activities of Triterpenoids from .

机构信息

College of Pharmacy, Henan University of Chinese Medicine, Zhengzhou 450046, China.

The Engineering and Technology Center for Chinese Medicine Development of Henan Province, Zhengzhou 450046, China.

出版信息

Molecules. 2022 Jul 29;27(15):4870. doi: 10.3390/molecules27154870.

Abstract

Five new triterpenoids, oenotheralanosterols C-G (-), with seven known triterpenoidcompounds, namely 2,3,19-trihydroxy-24-norurs4,12-dien-28-oic acid (), 3,23-dihydroxy-1-oxo-olean-12-en-28-oic acid (), remangilone C (), knoxivalic acid A (), termichebulolide (), rosasecotriterpene A (), androsanortriterpene C (), were extracted and separated from the dichloromethane part of L. The anti-pulmonary fibrosis activities of all the compounds against TGF-1-induced damage tonormal human lung epithelial (BEAS-2B) cells were investigated in vitro. The results showed that compounds , , , and exhibited significant anti-pulmonary fibrosis activities, with EC values ranging from 4.7 μM to 9.9 μM.

摘要

从 中提取并分离得到了五个新的三萜类化合物,oenotheralanosterols C-G (-),以及七个已知的三萜类化合物,分别是 2,3,19-三羟基-24-降乌苏 4,12-二烯-28-酸 ()、3,23-二羟基-1-氧代-齐墩-12-烯-28-酸 ()、remangilone C ()、knoxivalic 酸 A ()、termichebulolide ()、rosasecotriterpene A () 和 androsanortriterpene C ()。所有化合物对 TGF-β1 诱导的正常人类肺上皮细胞 (BEAS-2B) 损伤的体外抗肺纤维化活性进行了研究。结果表明,化合物 、 、 、 表现出显著的抗肺纤维化活性,EC 值范围为 4.7 μM 至 9.9 μM。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/9369581/460a26cafaa7/molecules-27-04870-g001.jpg

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