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从明日叶中提取的成分具有抗肿瘤促进作用。

Anti-tumor-promotion by principles obtained from Angelica keiskei.

作者信息

Okuyama T, Takata M, Takayasu J, Hasegawa T, Tokuda H, Nishino A, Nishino H, Iwashima A

机构信息

Department of Pharmacognosy and Phytochemistry, Meiji College of Pharmacy, Tokyo, Japan.

出版信息

Planta Med. 1991 Jun;57(3):242-6. doi: 10.1055/s-2006-960082.

Abstract

Potent anti-tumor promoter activity has been found in the nonpolar extracts of the root of "Ashita-Ba", Angelica keiskei Koidz. (Umbelliferae), which is eaten as a vegetable in Japan. From this active fraction, two angular furanocoumarins, archangelicin (1) and 8(S),9(R)-9-angeloyloxy-8,9-dihydrooroselol (2), three linear furanocoumarins, psoralen (3), bergapten (4) and xanthotoxin (5), and three chalcones, 4-hydroxyderricin (6), xanthoangelol (7) and a novel chalcone named ashitaba-chalcone (8), were isolated. Among these compounds, two angular type furanocoumarins, 1 and 2, and three chalcones, 6-8, suppressed 12-O-tetradecanoylphorbol-13-acetate (TPA)-stimulated 32Pi-incorporation into phospholipids of cultured cells, whereas coumarins 3-5 were less effective. In addition, chalcones 6 and 7 were proved to have anti-tumor-promoting activity in mouse skin carcinogenesis induced by 7,12-dimethylbenz[a]anthracene (DMBA) plus TPA. Since chalcones 6 and 7 showed calmodulin-interacting property, both chalcones may reveal anti-tumor-promoting activity via the modulation of calmodulin involved systems. These chalcones may be useful to develop the effective method for cancer prevention.

摘要

在日本作为蔬菜食用的明日叶(Angelica keiskei Koidz.,伞形科)根部的非极性提取物中发现了强效抗肿瘤促进活性。从该活性组分中,分离出两种角型呋喃香豆素,大天使内酯(1)和8(S),9(R)-9-当归酰氧基-8,9-二氢欧芹醇(2),三种线型呋喃香豆素,补骨脂素(3)、佛手柑内酯(4)和花椒毒素(5),以及三种查耳酮,4-羟基德里辛(6)、黄当归醇(7)和一种名为明日叶查耳酮(8)的新型查耳酮。在这些化合物中,两种角型呋喃香豆素1和2以及三种查耳酮6 - 8抑制了12-O-十四酰佛波醇-13-乙酸酯(TPA)刺激的32Pi掺入培养细胞的磷脂中,而香豆素3 - 5的效果较差。此外,查耳酮6和7在由7,12-二甲基苯并[a]蒽(DMBA)加TPA诱导的小鼠皮肤癌发生中被证明具有抗肿瘤促进活性。由于查耳酮6和7表现出与钙调蛋白相互作用的特性,这两种查耳酮可能通过调节涉及钙调蛋白的系统来揭示抗肿瘤促进活性。这些查耳酮可能有助于开发有效的癌症预防方法。

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