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来自红曲米的细胞毒性莫纳可林,红曲米是一种药食两用的中药材。

Cytotoxic monacolins from red yeast rice, a Chinese medicine and food.

作者信息

Zhang Zhihao, Ali Zulfiqar, Khan Shabana I, Khan Ikhlas A

机构信息

National Center for Natural Products Research, School of Pharmacy, University of Mississippi, University, MS 38677, United States.

National Center for Natural Products Research, School of Pharmacy, University of Mississippi, University, MS 38677, United States; Division of Pharmacognosy, Department of BioMolecular Sciences, School of Pharmacy, University of Mississippi, University, MS 38677, United States.

出版信息

Food Chem. 2016 Jul 1;202:262-8. doi: 10.1016/j.foodchem.2015.12.039. Epub 2015 Dec 10.

DOI:10.1016/j.foodchem.2015.12.039
PMID:26920293
Abstract

Seven new monacolins, monacolins Q-S (1-3), α,β-dehydromonacolin S (4), 3α-hydroxy-3,5-dihydromonacolin L (5), 3β-hydroxy-3,5-dihydromonacolin L (6), and α,β-hydromonacolin Q (7) were isolated and characterized from the methanol extract of red yeast rice. In addition, six known monacolins, α,β-dehydrodihydromonacolin K (8), dehydromonacolin K (9), dehydromonacolin L (10), monacolin K (11), dihydromonacolin K (12), dihydromonacolin L (13) and two compounds other than monacolins (14, 15) were also isolated. Structure elucidation of the isolates was achieved by means of NMR and mass spectroscopic data analyses. Compounds 1-5, 8, 9, 11, and 13 were evaluated for their cytotoxic activity against four cancer cell lines (SK-MEL, KB, BT-549, SK-OV-3) and two noncancerous kidney cell lines (LLC-PK1 and Vero). Monacolin Q (1), monacolin R (2) α,β-dehydrodihydromonacolin K (8), dehydromonacolin K (9), and monacolin K (11) showed cytotoxicity to most of these cell lines in terms of inhibition of cell proliferation. The cytotoxicity of monacolin K (11) was the most potent among all the tested monacolins.

摘要

从红曲米甲醇提取物中分离并鉴定出七种新的莫纳可林,即莫纳可林Q - S(1 - 3)、α,β - 脱氢莫纳可林S(4)、3α - 羟基 - 3,5 - 二氢莫纳可林L(5)、3β - 羟基 - 3,5 - 二氢莫纳可林L(6)和α,β - 氢化莫纳可林Q(7)。此外,还分离出六种已知的莫纳可林,α,β - 脱氢二氢莫纳可林K(8)、脱氢莫纳可林K(9)、脱氢莫纳可林L(10)、莫纳可林K(11)、二氢莫纳可林K(12)、二氢莫纳可林L(13)以及两种非莫纳可林类化合物(14, 15)。通过核磁共振和质谱数据分析对分离物进行结构解析。对化合物1 - 5、8、9、11和13针对四种癌细胞系(SK - MEL、KB、BT - 549、SK - OV - 3)和两种非癌性肾细胞系(LLC - PK1和Vero)进行细胞毒性活性评估。莫纳可林Q(1)、莫纳可林R(2)、α,β - 脱氢二氢莫纳可林K(8)、脱氢莫纳可林K(9)和莫纳可林K(11)在抑制细胞增殖方面对大多数这些细胞系显示出细胞毒性。莫纳可林K(11)的细胞毒性在所有测试的莫纳可林中最为显著。

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