Kil Yun-Seo, Choi Seul-Ki, Lee Yun-Sil, Jafari Mahtab, Seo Eun-Kyoung
College of Pharmacy, Graduate School of Pharmaceutical Sciences, Ewha Womans University , Seoul 120-750, Korea.
Department of Pharmaceutical Sciences, University of California , Irvine, California 92697, United States.
J Nat Prod. 2015 Oct 23;78(10):2481-7. doi: 10.1021/acs.jnatprod.5b00633. Epub 2015 Oct 2.
Five new chalcones, 4,2',4'-trihydroxy-3'-[(2E,5E)-7-methoxy-3,7-dimethyl-2,5-octadienyl]chalcone (1), (±)-4,2',4'-trihydroxy-3'-[(2E)-6-hydroxy-7-methoxy-3,7-dimethyl-2-octenyl]chalcone (2), 4,2',4'-trihydroxy-3'-[(2E)-3-methyl-5-(1,3-dioxolan-2-yl)-2-pentenyl]chalcone (3), 2',3'-furano-4-hydroxy-4'-methoxychalcone (4), and (±)-4-hydroxy-2',3'-(2,3-dihydro-2-methoxyfurano)-4'-methoxychalcone (5), were isolated from the aerial parts of Angelica keiskei Koidzumi together with eight known chalcones, 6-13, which were identified as (±)-4,2',4'-trihydroxy-3'-[(6E)-2-hydroxy-7-methyl-3-methylene-6-octenyl]chalcone (6), xanthoangelol (7), xanthoangelol F (8), xanthoangelol G (9), 4-hydroxyderricin (10), xanthoangelol D (11), xanthoangelol E (12), and xanthoangelol H (13), respectively. Chalcones 1-13 were evaluated for their promoter activity on heat shock protein 25 (hsp25, murine form of human hsp27). Compounds 1 and 6 activated the hsp25 promoter by 21.9- and 29.2-fold of untreated control at 10 μM, respectively. Further protein expression patterns of heat shock factor 1 (HSF1), HSP70, and HSP27 by 1 and 6 were examined. Compound 6 increased the expression of HSF1, HSP70, and HSP27 by 4.3-, 1.5-, and 4.6-fold of untreated control, respectively, without any significant cellular cytotoxicities, whereas 1 did not induce any expression of these proteins. As a result, 6 seems to be a prospective HSP inducer.
从明日叶的地上部分分离出5种新的查耳酮,分别为4,2',4'-三羟基-3'-[(2E,5E)-7-甲氧基-3,7-二甲基-2,5-辛二烯基]查耳酮(1)、(±)-4,2',4'-三羟基-3'-[(2E)-6-羟基-7-甲氧基-3,7-二甲基-2-辛烯基]查耳酮(2)、4,2',4'-三羟基-3'-[(2E)-3-甲基-5-(1,3-二氧戊环-2-基)-2-戊烯基]查耳酮(3)、2',3'-呋喃基-4-羟基-4'-甲氧基查耳酮(4)和(±)-4-羟基-2',3'-(2,3-二氢-2-甲氧基呋喃基)-4'-甲氧基查耳酮(5),同时还分离出8种已知的查耳酮6 - 13,它们分别被鉴定为(±)-4,2',4'-三羟基-3'-[(6E)-2-羟基-7-甲基-3-亚甲基-6-辛烯基]查耳酮(6)、黄当归醇(7)、黄当归醇F(8)、黄当归醇G(9)、4-羟基德里辛(10)、黄当归醇D(11)、黄当归醇E(12)和黄当归醇H(13)。对查耳酮1 - 13进行了它们对热休克蛋白25(hsp25,人hsp27的小鼠形式)启动子活性的评估。化合物1和6在10 μM时分别将hsp25启动子激活至未处理对照的21.9倍和29.2倍。进一步检测了化合物1和6对热休克因子1(HSF1)、HSP70和HSP27的蛋白质表达模式。化合物6分别将HSF1、HSP70和HSP27的表达增加至未处理对照的4.3倍、1.5倍和4.6倍,且无任何明显的细胞毒性,而化合物1未诱导这些蛋白质的任何表达。结果表明,化合物6似乎是一种有前景的热休克蛋白诱导剂。