• 제목/요약/키워드: Dammar

검색결과 13건 처리시간 0.019초

사천 구암 출토 미투리 보존처리 (Conservation Treatment of Mituri (hemp shoes) of the Choseon Dynasty in Sacheon, South Korea)

  • 송지애;정아름
    • 보존과학연구
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    • 통권34호
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    • pp.50-61
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    • 2013
  • 사천 구암 발굴현장 내 출토된 조선시대 회곽묘에서 복식류와 함께 미투리가 출토되었다. 미투리는 목재와 초본류로 제작된 복합재질로 앞총부가 소실되거나 매우 약한 상태로 수습되었다. 보존처리를 위하여 미투리에 대한 과학적 재질분석과 강화제 선정 예비실험을 먼저 진행하였다. 재질 분석 결과, 미투리는 벼속(Oryza spp.), 마섬유, 쌍자엽식물 1종이 사용됨을 확인하였으며 또한 뒤쪽 도갱이에 붙어있었던 직물은 면섬유로 분석되었다. 강화제 선정을 위해 약품 5종(Polyethylene Glycol, Paraloid-B72, Dammar gum, Methyl Cellulose, Silicone resin)을 선정하여 예비실험을 실시하였다. 색차, 광택성, 내절강도와 인장강도 변화를 약품별로 측정하여 결과를 비교하여 PEG를 강화제로 선정하였다. PEG는 색도 및 광택변화가 적고, 인장강도가 높게 확인되어 가장 적합한 것으로 판단되었다. 미투리 보존처리는 클리닝 후 PEG 4000을 5%에서 80%까지 농도를 높여 유물에 견고성을 부여하였으며 조절건조를 통해 보존처리를 완료하였다.

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Ginsenoside $Rg_5$, A Genuine Dammarane Glycoside from Korean Red Ginseng

  • Kim, Shin-Il;Park, Jeong-Hill;Ryu, Jae-Ha;Park, Jong-Dae;Lee, You-Hui;Park, Jae-Hyun;Kim, Tae-Hee;Kim, Jong-Moon;Baek, Nam-In
    • Archives of Pharmacal Research
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    • 제19권6호
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    • pp.551-553
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    • 1996
  • A genuine dammarane glycoside, named ginsenoside $Rg_{5}$, has been isolated by repeated column chromatography and preparative HPLC from the MeOH extract of Korean red ginseng (Panax ginseng C.A. Meyer). The chemical structure of ginsenoside$ Rg_{5}$ was determined as $3-O-[{\beta}-D-glucopyranosyl (1{\rightarrow}2)-{\beta}-D-glucopyranosyl]$ dammar-20(22), $24-diene-3{\beta},12{\beta}-diol$ by spectral and chemical methods. The stereostructure of a double bond at C-20(22) of ginsenoside $Rg_{5}$ was characterized as (E) from the chemical shift of C-21 in the $^{13}C-NMR $and a NOESY experiment in the $^{1}H-NMR$.

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Identification of Dammarane-type Triterpenoid Saponins from the Root of Panax ginseng

  • Lee, Dong Gu;Lee, Jaemin;Yang, Sanghoon;Kim, Kyung-Tack;Lee, Sanghyun
    • Natural Product Sciences
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    • 제21권2호
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    • pp.111-121
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    • 2015
  • The root of Panax ginseng, is a Korea traditional medicine, which is used in both raw and processed forms due to their different pharmacological activities. As part of a continued chemical investigation of ginseng, the focus of this research is on the isolation and identification of compounds from Panax ginseng root by open column chromatography, medium pressure liquid chromatography, semi-preparative-high performance liquid chromatography, Fast atom bombardment mass spectrometric, and nuclear magnetic resonance. Dammarane-type triterpenoid saponins were isolated from Panax ginseng root by open column chromatography, medium pressure liquid chromatography, and semi-preparative-high performance liquid chromatography. Their structures were identified as protopanaxadiol ginsenosides [gypenoside-V (1), ginsenosides-Rb1 (2), -Rb2 (3), -Rb3 (4), -Rc (5), and -Rd (6)], protopanaxatriol ginsenosides [20(S)-notoginsenoside-R2 (7), notoginsenoside-Rt (8), 20(S)-O-glucoginsenoside-Rf (9), 6-O-[$\alpha$-L-rhamnopyranosyl(1$\rightarrow$2-$\beta$-D-glucopyranosyl]-20-O-$\beta$-D-glucopyranosyl-$3\beta$,$12\beta$, 20(S)-dihydroxy-dammar-25-en-24-one (10), majoroside-F6 (11), pseudoginsenoside-Rt3 (12), ginsenosides-Re (13), -Re5 (14), -Rf (15), -Rg1 (16), -Rg2 (17), and -Rh1 (18), and vinaginsenoside-R15 (19)], and oleanene ginsenosides [calenduloside-B (20) and ginsenoside-Ro (21)] through the interpretation of spectroscopic analysis. The configuration of the sugar linkages in each saponin was established on the basic of chemical and spectroscopic data. Among them, compounds 1, 8, 10, 11, 12, 19, and 20 were isolated for the first time from P. ginseng root.