• 제목/요약/키워드: diterpene

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한국산(韓國産) 부자류(附子類) 생약(生藥)에 관한 연구 (V). -진범 지하부의 성분(成分)에 대하여- (Studies on Korean Aconitum Species(V). -On the Chemical Constituents of Aconitum pseudolaeve var. erectum-)

  • 이현선;정보섭
    • 생약학회지
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    • 제20권1호
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    • pp.6-9
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    • 1989
  • A new aromatic amide, methyl-N-(3-carbamoylpropionyl) anthranilate was isolated for the first time as a natural compound and one known $C_{19}-diterpene\;alkaloid$, avadharidine was also obtained from the root of Aconitum pseudolaeve var. erectum. The\;LD_{50}$ values of water extract and MeOH extract of the root of Aconitum pseudolaeve var. erectum in mice were 1. 23 g (13. 6 g crude drug) and 0. 77 g(5. 13 g crude drug)/kg, p.o., respectively.

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Lsolation of Diterpene acid from Anisotome Lyallii

  • Lim Jin A;Choi Young;Oh In Kio;Kim Hyung Min;Kim Young Ok;Perry Nigel B;Baek Seung Hwa
    • 동의생리병리학회지
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    • 제17권4호
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    • pp.1112-1115
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    • 2003
  • The diterpene acid 1 was isolated from the roots of Anisotome lyallii(Apiaceae/Umbelliferae). The structure of the compound was elucidated as anisotomenoic acid 1 on the basis of spectroscopic methods. This compound was evaluated against P388 murine leukaemia and B 16/F10 melanoma cells.

천연 diterpenoids에 대하여 (Diterpenoids)

  • 한구동
    • 약학회지
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    • 제17권4호
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    • pp.179-216
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    • 1973
  • Diterpenoid늬 연구현황은 본인의 회갑기념논문집에 기재한바 있으나 그후 수년이 경과하여 많은 논문이 발표되어 있으므로 입수된 문헌범위내에서 이를 보충하여 천연 diterpene의 분포, 생합성, 생물학적 중요성 및 이용에 관한 연구등에 대하여 이하 기술코저 한다.

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Diterpene Constituents from Aster oharai

  • Kwon, Hak-Cheol;Yi, Jae-Hun;Lee, Kang-Ro
    • 대한약학회:학술대회논문집
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    • 대한약학회 2000년도 NEW STRATEGY FOR DRUG DEVELOPMENT IN POST-GENOMIC ERA(대한약학회)
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    • pp.238.1-238.1
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    • 2000
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Kaurenoic acid, a Diterpene Derived from Aralia continentalis, Alleviates Lipogenesis in HepG2 Cells

  • Kim, Yu Gon;Kim, Jae Hyeon;Jo, Yong Wan;Kwun, Min Jung;Han, Chang Woo
    • 대한한의학회지
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    • 제36권4호
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    • pp.74-79
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    • 2015
  • Objectives: Here we investigated the anti-lipogenic potential of kaurenoic acid (KA), a diterpene derived from Aralia continentalis, in a cellular model of non-alcoholic fatty liver disease. Methods: HepG2 cells were treated with palmitate for 24h to induce intracellular lipid accumulation. To assess the influence of KA on steatotic HepG2 cells, various concentration of KA was co-administered. After palmitate treatment, Intracellular triglyceride content was measured. Expression level of several lipogenic genes, sterol regulatory element-binding transcription factor-1c (SREBP-1c), acetyl-CoA carboxylase (ACC), fatty acid synthase (FAS), and stearoyl-CoA desaturase-1 (SCD-1) were measured using Western-blot analyses or RT-PCR. Results: Palmitate markedly increased intracellular triglyceride level and expression of related lipogenic genes in HepG2 cells, and which was relieved by co-administered KA. Conclusions: It is conceivable that that KA may have a pharmacological potential to reduce lipid accumulation in non-alcoholic fatty liver disease.