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蛇床子果实中的新香豆素类化合物及抗炎成分。

New coumarins and anti-inflammatory constituents from the fruits of Cnidium monnieri.

作者信息

Lee Tzong-Huei, Chen Yuan-Chih, Hwang Tsong-Long, Shu Chih-Wen, Sung Ping-Jyun, Lim Yun-Ping, Kuo Wen-Lung, Chen Jih-Jung

机构信息

Graduate Institute of Pharmacognosy, Taipei Medical University, Taipei 110, Taiwan.

Department of Pharmacy & Graduate Institute of Pharmaceutical Technology, Tajen University, Pingtung 907, Taiwan.

出版信息

Int J Mol Sci. 2014 May 28;15(6):9566-78. doi: 10.3390/ijms15069566.

Abstract

The fruit of Cnidium monnieri is commercially used as healthcare products for the improvement of impotence and skin diseases. Three new coumarins, 3'-O-methylmurraol (1), rel-(1'S,2'S)-1'-O-methylphlojodicarpin (2), and (1'S,2'S)-1'-O-methylvaginol (3), have been isolated from the fruits of C. monnieri, together with 14 known compounds (4-17). The structures of these new compounds were determined through spectroscopic and MS analyses. Compounds 1, 4-12, and 14-17 exhibited inhibition (IC50 ≤ 7.31 µg/mL) of superoxide anion generation by human neutrophils in response to formyl-l-methionyl-l-leucyl-l-phenylalanine/cytochalasin B (fMLP/CB). Compounds 7, 9-11, 15, and 17 inhibited fMLP/CB-induced elastase release with IC50 values ≤7.83 µg/mL. This investigation reveals that bioactive isolates (especially 6, 7, 14, and 17) could be further developed as potential candidates for the treatment or prevention of various inflammatory diseases.

摘要

蛇床子的果实作为改善阳痿和皮肤病的保健品在商业上有应用。从蛇床子果实中分离出了三种新的香豆素,即3'-O-甲基莫雷醇(1)、反式-(1'S,2'S)-1'-O-甲基弗洛乔迪卡品(2)和(1'S,2'S)-1'-O-甲基阴道醇(3),以及14种已知化合物(4 - 17)。这些新化合物的结构通过光谱和质谱分析确定。化合物1、4 - 12以及14 - 17对人中性粒细胞因甲酰基-L-蛋氨酰-L-亮氨酰-L-苯丙氨酸/细胞松弛素B(fMLP/CB)刺激产生超氧阴离子具有抑制作用(IC50≤7.31μg/mL)。化合物7、9 - 11、15和17以IC50值≤7.83μg/mL抑制fMLP/CB诱导的弹性蛋白酶释放。该研究表明,具有生物活性的分离物(尤其是6、7、14和17)可进一步开发成为治疗或预防各种炎症性疾病的潜在候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0667/4100110/313442a45052/ijms-15-09566-g001.jpg

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