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来自恒春厚壳桂的酚类化合物:它们的细胞毒性和酪氨酸激酶抑制特性。

Phenolic compounds from Cryptocarya konishii: their cytotoxic and tyrosine kinase inhibitory properties.

作者信息

Kurniadewi Fera, Juliawaty Lia D, Syah Yana M, Achmad Sjamsul A, Hakim Euis H, Koyama Kiyotaka, Kinoshita Kaoru, Takahashi Kunio

机构信息

Natural Products Research Group, Department of Chemistry, Bandung Institute of Technology, Jalan Ganeca 10, Bandung, Indonesia.

出版信息

J Nat Med. 2010 Apr;64(2):121-5. doi: 10.1007/s11418-009-0368-y. Epub 2009 Dec 11.

Abstract

Two chalcone derivatives, 2'-hydroxychalcone (1) and desmethylinfectocaryone (2), together with five known phenolic compounds infectocaryone (3), cryptocaryone (4), kurzichalcolactone A (5), pinocembrin (6) and trans-N-feruloyltyramine (7), were isolated from the methanol extract of the wood of Cryptocarya konishii. The structures of the new compounds were determined based on the analysis of spectroscopic data, including UV, IR, 1D and 2D NMR, and mass spectra. Evaluation of the cytotoxic and tyrosine kinase inhibitory activities of compounds 1-7 showed that compounds 2-4 strongly inhibited the growth of murine leukemia P-388 cells, whereas compound 4 significantly inhibited the enzyme.

摘要

从红楠木材的甲醇提取物中分离出两种查尔酮衍生物,即2'-羟基查尔酮(1)和去甲基感染核酮(2),以及五种已知的酚类化合物感染核酮(3)、隐核酮(4)、短叶查尔酮内酯A(5)、松属素(6)和反式-N-阿魏酰酪胺(7)。通过对紫外、红外、一维和二维核磁共振以及质谱等光谱数据的分析确定了新化合物的结构。对化合物1-7的细胞毒性和酪氨酸激酶抑制活性的评估表明,化合物2-4强烈抑制小鼠白血病P-388细胞的生长,而化合物4显著抑制该酶。

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