• 생약학회지
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• 제16권3호
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• pp.155-159
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• 1985

Isomotiol $(fern-8-en-3{\beta}-ol)$ was isolated from the n-hexane fraction of Euphorbia supina Rafin. The structure of isomotiol was identified by IR, NMR, Mass spectra and compared with the authentic sample. Isomotiol was first isolated from the family of Euphorbiaceae.

• 생약학회지
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• 제38권3호통권150호
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• pp.291-295
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• 2007

Eight compounds were isolated from the whole plants of Euphorbia supina (Euphorbiaceae) through repeated silica gel, YMC gel and Sephadex LH-20 column chromatography. Their chemical structures were elucidated as 7-hydroxy-6-methoxycoumarin (scopoletin) (1), p-hydroxybenzaldehyde (2), methyl gallate (3), gallic acid (4), quercetin (5), quercetin $3-O-{\alpha}-L-arabinofuranoside$ (avicularin) (6), kaempferol $3-O-{\alpha}-L-arabinofuranoside$ (juglanin) (7) and kaempferol $3-O-{\beta}-D-glucopyranoside$ (astragaline) (8) by spectroscopic (NMR and MS) analysis.

• Natural Product Sciences
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• 제21권3호
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• pp.176-184
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• 2015

In our search for natural soluble epoxide hydrolase (sEH) inhibitors from plants, an extract of the dried whole plants of Euphorbia supina Rafin was found to significantly inhibit sEH activity in vitro. Phytochemical investigation of E. supina resulted in isolation of 17 compounds (1 - 17), including triterpenes (1 - 4), phenolic compounds (5 - 8), and flavonoid derivatives (9 - 17). The structures of the isolated compounds were established mainly by extensive analysis of the 1D and 2D NMR, and MS data. All of the isolated compounds were evaluated for their sEH inhibitory activity. Among the isolated phenolic compounds, 8 was identified as a significant inhibitor of sEH, with an IC₅₀ value of 15.4 ± 1.3 μM. Additionally, a kinetic analysis of isolated compounds (2, 5, 8 - 11, 13, and 17) indicated that the inhibitory effects of flavonoid derivatives 10 and 11 were of mixed-type, with inhibitory constants (K_i) ranging from 3.6 ± 0.8 to 21.8 ± 1.0 μM, whereas compounds 2, 5, 8, 9, 13, and 17 were non-competitive inhibitors with inhibition K_i values ranging from 3.3 ± 0.2 to 39.5 ± 0.0 μM.

• 한국식품영양과학회지
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• 제40권4호
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• pp.486-492
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• 2011

본 연구는 애기땅빈대(Euphorbia supina Rafin.) 열수(ESW) 및 에탄올 추출물(ESE)의 항염증 효과를 조사하기 위하여 RAW 264.7 세포에서 LPS에 의해 생성되는 염증매개물질에 대한 억제효과를 조사하였다. ESW와 ESE은 조사된 모든 농도에서 95% 이상의 생존율을 보여 세포독성이 없는 것으로 확인되었다. ESW의 경우, NO의 생성을 100, 250, 500, $1000\;{\mu}g$/mL 농도에서 각각 21.6%, 31.9%, 44.3%, 54.8% 억제하였고, PGE2의 생성은 250, 500, $1000\;{\mu}g$/mL 농도에서 각각 25.7%, 34%, 38.2% 억제하여 농도 의존적이고 유의적인 억제효과가 확인되었다. IL-6의 생성은 250, $1000\;{\mu}g$/mL 농도에서 각각 66.1%, 54.3% 억제하였다. IL-10, TNF-${\alpha}$의 생성은 $500\;{\mu}g$/mL 농도에서 유의적인 증가를 나타냈다. ESE의 경우, NO의 생성을 100, 250, 500, $1000\;{\mu}g$/mL 농도에서 각각 38.3%, 66%, 74.7%, 77.5%, $PGE_2$의 생성은 100, 250, 500, $1000\;{\mu}g$/mL 농도에서 각각 40%, 51.8%, 92.4%, 94.7% 농도 의존적이고 유의적으로 억제하였다. IL-6의 생성은 100, 250, 500, $1000\;{\mu}g$/mL 농도에서 각각 43.9%, 48.9%, 69.7%, 89.4% 억제하였다. IL-10의 생성은 $500\;{\mu}g$/mL 농도에서 44.1% 억제하였고, TNF-${\alpha}$의 생성은 $1000\;{\mu}g$/mL 농도에서 92.4% 억제하였다. 결과를 종합해 볼때, 애기땅빈대는 ESW보다는 ESE의 경우가 LPS로 활성화된 RAW 264.7 대식세포에서의 염증매개물질 억제효과가 좋은 것으로 나타났으며, ESE는 저농도보다는 $500\;{\mu}g$/mL 이상의 고농도에서 NO, $PGE_2$, IL-6, IL-10, TNF-${\alpha}$와 같은 염증매개물질 억제효과가 좋은 것으로 확인되었다. 따라서 애기땅빈대 ESE는 $500\;{\mu}g$/mL 농도 이상에서 염증매개물질 억제 보조제로서 활용될 수 있을 것으로 사료된다.