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Sesquiterpenoids and 2-(2-Phenylethyl)chromone Derivatives from the Resinous Heartwood of Aquilaria sinensis

机译:Sesquiterpenoids和2-(2-苯基乙基)铬酮衍生物来自<斜视> Aquilaria sinensis的树脂心材

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Graphic Abstract One novel spirolactone, aquilarisinolide ( 1 ), three new sesquiterpenoids, (2 R ,4 S ,5 R ,7 R )-2-hydroxyeremophila-9,11-dien-8-one ( 2 ), (1 R ,4 S ,5 S ,7 R ,11 R )-13-hydroxyepidaphnauran-9-en-8-one ( 3 ), and (4 R ,5 S ,7 R ,8 S ,10 S ,13 R )-8,13-dihydroxyrotunda-1,11-dien-3-one ( 4 ), together with 13 known compounds ( 5 – 17 ) were isolated from the resinous heartwood of Aquilaria sinensis (Thymelaeaceae). The structures of the new compounds were elucidated based on the analysis of NMR and MS data and theoretical calculations their ECD spectra. The isolated compounds were evaluated for their protective activities against PC12 cell injury induced by corticosterone (CORT) and 1-methyl-4-phenylpyridine ion (MPP ~(+)), as well as inhibitory activities against BACE1. Compound 4 , 5,6-dihydroxy-2-(2-phenylethyl)chromone ( 5 ), daphnauranol B ( 7 ), 6-methoxy-2-[2-(3-methyoxyphenyl)ethyl]chromone ( 10 ), isoagarotetrol ( 14 ), and 1-hydroxy-1,5-diphenylpentan-3-one ( 16 ) showed significant protective effects on CORT-induced injury in PC12 cells at a concentration of 20?μM ( P ?&?0.001). Isoagarotetrol ( 14 ) showed a significant protective effect on MPP ~(+)-induced injury in PC12 cells at a concentration of 20?μM ( P ?&?0.001), while compound 4 showed a moderate activity ( P ?&?0.01). The BACE1-inhibitory activities of all tested compounds were very weak with less than 30% inhibition at a concentration of 20?μM. Supplementary Information The online version contains supplementary material available at 10.1007/s13659-021-00313-0.
机译:图形摘要一部分新型螺旋体,Aigilarisinolide(1),三种新的倍二萜类化合物,(2 R,4 S,5 R,7 R)-2-羟基汞合金 - 9,11-Dien-8-一(2),(1 R, 4 s,5 s,7 r,11 r)-13-羟基哌丹-9-en-8-one(3),(4 r,5 s,7 r,8 s,10 s,13 r)-8 ,13-二羟基吡坦-1,11-DIEN-3-one(4)与13种已知的化合物(5-17)与Aquilaria Sinensis(Thymelaeacee)的树脂心材分离出来。基于NMR和MS数据的分析和其ECD光谱的理论计算阐明了新化合物的结构。评估分离的化合物对由皮质酮(CORT)和1-甲基-4-苯基吡啶离子(MPP〜(+))的PC12细胞损伤的保护活性,以及​​对BACE1的抑制活性。化合物4,5,6-二羟基-2-(2-苯基乙基)铬酮(5),二烷酰胺B(7),6-甲氧基-2- [2-(3-甲氧氧基苯基)乙基]铬酮(10),异冈毒素( 14)和1-羟基-1,5-二苯基戊烷-3-一(16)对PC12细胞的皮质诱导损伤的显着保护作用,其浓度为20Ωμm(p?&amp; 0.001)。胰岛素(14)对MPP〜(+)诱导的PC12细胞造成的浓度的浓度为20≤μm(p≤≤00.<0.001),而化合物4显示了中等活动(P?&amp ; ?0.01)。所有测试化合物的Bace1抑制活性非常弱,浓度为20μm的浓度小于30%。补充信息在线版本包含10.1007 / S13659-021-00313-0的补充材料。

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