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The new triterpene glycoside zygoeichwaloside G was isolated from the roots of Zygophyllum eichwaldii C.A.M. by column chromatography. Acid hydrolysis and PMR and 13C NMR spectroscopy using twodimensional COSY, TOCSY, and HSQC and analysis of HMBC and ROESY spectra established that glycoside G is 19--hydroxyursolic acid 3-O--L-(2-O-sulfo)-arabinopyranoside.  相似文献   
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The chemical composition of the essential oil from the aerial parts of three Lamiaceae species from Uzbekistan was investigated by GC-MS analysis. β-Linalool (26.6%), α-terpineol (10.0%), coumarin (8.9%) and 4,5,7,7α-tetrahydro-4,4,7α-trimethyl-2(6H)-benzofuranone (5.4%) resulted as the main components of Ajuga turkestanica essential oil, while camphene (17.1%), 1,8-cineole (15.9%), β-cymene (7.9%) and limonene (7.4%) in Phlomis regelii. The essential oil of Thymus seravschanicus was dominated by thymol (37.5%), phellandral (26.0%), τ-terpinene (6.6%) and β-cymene (5.2%). The essential oils had considerable antimicrobial activity against different bacterial strains and fungi. Among the tested samples of essential oils, P. regelii essential oil has the significant antioxidant activity with IC50 value of 117.8 ± 8.02 μg/mL.  相似文献   
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The chemical composition of lipid extracts from aerial parts of Zygophyllum oxianum was determined by GC and TLC. The yield of total lipids was 0.75% in leaves, 0.33% in stems, and 0.49% in fruit calculated for fresh plant mass. Phospholipids were represented by nine classes, of which phosphatidylcholine dominated (55.8% in leaves, 56.4% in stems, 63.7% in fruit of total PL). The n-BuOH extract from the plant aerial part exhibited noticeable antifungal activity. The CHCl3:MeOH (2:1) extract from leaves and stems exhibited pronounced in vitro cytotoxicity against human bladder carcinoma cell line 5637 with IC50 6.2 μg/mL.  相似文献   
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Column chromatography of roots ofZygophyllum eichwaldiiC.A.M. (Zygophyllaceae) afforded the new glycoside zygoeichwaloside I. Acid hydrolysis, alkaline saponification, solvolysis, and 1 H and 13 C NMR spectroscopies using COSY, TOCSY, ROESY, HSQC, and HMBC methods established its structure as the 28-O--D-glucopyranosyl ester of pomolic acid 3-O--D-2-O-sulfonylgalactopyranoside.  相似文献   
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