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Sessilifol A and B, Urease Inhibitory Pimarane-type Diterpenes from Hymenocrater sessilifolius

机译:Sessilifol A和B,来自Hymenocarater Sessilifolius的脲酶抑制术型Diterpenes

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摘要

New pimarane type diterpenes named sessilifol A (1) and B (2) have been isolated from the EtOH soluble fraction of Hymenocrater sessilifolius Benth., along with eight known constituents cirsimaritin (3), gardenin C (4), beta-sitosterol (5), saringosterol (6), beta-sitosterol glucoside (7), ursolic acid (8), sucrose (9) and vanillic acid (10). Their structures were elucidated on the basis of H-1- and C-13-NMR spectra and by 2D-NMR experiments. The structure of 1 was further confirmed by single crystal X-ray diffraction technique. The compound 2 showed potent inhibitory potential against the enzyme urease while 1, 3, 4 and 10 were moderately active.
机译:名为Sessilifol A(1)和B(2)的新的Pimarane型Diterpenes已从Hymenocater Sessilifolius Benth的EtOH可溶性分数中分离出来。以及八个已知的成分Cirsimaritin(3),Gardenin C(4),Beta-sitosterol(5 ),Saringosterol醇(6),β-谷甾醇糖苷(7),尿溶胶(8),蔗糖(9)和香草酸(10)。 它们的结构在H-1-和C-13-NMR光谱和2D-NMR实验的基础上阐明。 通过单晶X射线衍射技术进一步证实了1的结构。 化合物2对酶脲酶的有效的抑制电位显示为1,3,4和10的中度活性。

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