• 제목/요약/키워드: Elsholtzia bodinieri

검색결과 3건 처리시간 0.014초

Triterpenoid Saponins from Elsholtzia bodinieri

  • Hu, Hao-Bin;Zheng, Xu-Dong;Hu, Huai-Sheng;Jian, Yu-Feng
    • Bulletin of the Korean Chemical Society
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    • 제28권9호
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    • pp.1519-1522
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    • 2007
  • A new oleanane-type triterpenoid estersaponin, bodinierin C (1), along with two known saponins, mazusaponin I (2) and ciwujianoside C (3), were isolated from the water-soluble part of the root barks of Elsholtzia bodinieri. The structure of bodinierin C was characterized by spectroscopic means and chemical hydrolysis as 3β -Ocaffeoyl- 23-hydroxylechinocystic acid 28-O-α -L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β- D-glucopyranosyl ester. The known compounds were identified by comparing their spectral data with those of authentic samples or data reported in the literature. All compounds were firstly isolated from Elsholtzia bodinieri family.

중국 약용식물 추출물의 알도즈 환원 효소 억제 효능 검색 (VII) (Screening of Chinese Herbal Medicines with Inhibitory Effect on Aldose Reductase (VII))

  • 이윤미;김영숙;김주환;김진숙
    • 생약학회지
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    • 제44권2호
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    • pp.161-167
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    • 2013
  • Aldose reductase (AR) has been shown to play an important role in the development of the diabetic complications. To discover novel treatments for diabetic complications from natural sources, 59 Chinese herbal medicines have been investigated for inhibitory activities on AR. Among them, 10 herbal medicines, Catalpa fargesii (stem and leaf), Saussurea Laniceps(whole plant), Alnus nepalensis(stem and leaf), Swertia macrosperma (whole plant), Woodfordia fruticosa (stem and leaf), Elsholtzia bodinieri (whole plant), Elsholtzia fruticosa (whole plant), Rosa multiflora (fruit), Nardostachys chinensis (whole plant), Eurya groffii (stem and leaf) exhibited a significant inhibitory activity compared with 3,3-tetramethyleneglutaric acid (TMG) as positive control. Particularly, 4 herbal medicines, C. fargesii (stem and leaf), S. Laniceps (whole plant), A. nepalensis (stem and leaf), S. macrosperma (whole plant) showed two times more potent inhibitory activity than TMG ($5.37{\mu}g/ml$).