• 제목/요약/키워드: Natural plant products

검색결과 626건 처리시간 0.026초

산조인 (酸棗仁)의 Flavonoid성분 (Flavonoids from the Seeds of Zizyphus jujuba var. spinosa)

  • 이소영;이주영;김주선;이제현;강삼식
    • 생약학회지
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    • 제43권2호
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    • pp.127-136
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    • 2012
  • Eight flavonoids were isolated from the BuOH fraction of the 70% EtOH extract of Zizyphus jujuba var. spinosa seeds along with three known compounds, daucosterol (1), butyl ${\beta}$-D-fructofuranoside (2), and magnoflorine (4). On the basis of spectroscopic methods and comparison with literature values their structures were elucidated as 6"'-feruloylspinosin (3), nicotiflorin (5), 6"'-p-coumaroylspinosin (6), isospinosin (7), 6"'-vanilloylspinosin (8), spinosin (9), hovetrichoside C (10), and camelliaside B (11). Compounds 1, 2, 10, and 11 were isolated from this plant for the first time.

작약(芍藥)의 성분연구(成分硏究) (3);Triterpenoid의 분리 (Phytocheical Studies on Paeoniae Radix (3);Triterpenoids)

  • 김주선;김윤정;이소영;강삼식
    • 생약학회지
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    • 제39권1호
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    • pp.37-42
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    • 2008
  • From the 70% EtOH extract from the roots of Paeonia lactiflora (Paeoniaceae), nine triterpenoids were isolated and identified as ${\beta}-amyrin$ (1), 24-methylenecycloartanol (2), betulinic acid (3), oleanolic acid (4), hederagenin (5), 30-norhederagenin (6), 30-norarjunolic acid (7), arjunolic acid (8), and $3{\beta},4{\beta},23-trihydroxy-24,30-dinorolean-12,20(29)-dien-28-oic$ acid (9) by spectroscopic methods. Among these compounds, 1, 2, 7, 8 and 9 were isolated for the first time from this plant.

작약(芍藥)의 성분연구(成分硏究) (2);Phenol성 물질 및 관련화합물들의 분리 (Phytochemical Studies on Paeoniae Radix (2);Phenolic and Related compounds)

  • 김주선;김윤정;이주영;강삼식
    • 생약학회지
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    • 제39권1호
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    • pp.28-36
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    • 2008
  • From the 70% EtOH extract of Paeonia lactiflora roots (Paeoniaceae), fourteen phenolic and related compounds were isolated. They were identified as ${\alpha}-tocopherol$ (1), dioctylphthalate (2), ${\alpha}-tocospiro$ B (3), paeonol (4), 3,3'-di-O-methylellagic acid(5), 3,4'-di-O-methylellagic acid (6), benzoic acid (7), aromadendrin (8), p-hydroxybenzoic acid (9), (+)-catechin (10), gallic acid (11), nicotinamide (12), methyl gallate (13) and $1,2,3,4,6-penta-O-galloyl-{\beta}-D-glucose$ (14) by spectroscopic methods. Among these compounds, 1-3, 5, 6, 8 and 12 were isolated for the first time from this plant.

작약(芍藥)의 성분연구(成分硏究) (1);Monoterpene glucoside의 분리 (Phytochemical Studies on Paeoniae Radix (1);Monoterpene Glucosides)

  • 연민혜;이주영;김주선;강삼식
    • 생약학회지
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    • 제39권1호
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    • pp.19-27
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    • 2008
  • From the polar fractions of 70% EtOH extract of Paeonia lactiflora roots (Paeoniaceae), ten monoterpene glucosides were isolated and identified as lactiflorin (1), benzoylpaeoniflorin (2), mudanpioside C (3), $1-O-{\beta}-D-glucosylpaeonisuffrone$ (4), paeonidanin (5), $1-O-{\beta}-D-glucosyl-8-O-benzoylpaeonisuffrone$ (6), paeoniflorin (7), albiflorin (8), oxypaeoniflorin (9) and mudanpioside E (10) by spectroscopic methods. Among these glucosides, 3-6 and 10 were isolated for the first time from this plant.

Studies on the Anti-inflammatory Activity of Aralia continentalis (III)

  • Han, Byung-Hoon;Woo, Eun-Rhan;Park, Myung-Hwan;Han, Young-Nam
    • Archives of Pharmacal Research
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    • 제8권2호
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    • pp.59-65
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    • 1985
  • Besides (-) pimara-8(14), 15-dien-19-oic acid [I] which had already been isolated as an active anti-inflammtory principle of Aralia continentalis, (-) kaur-16-en-19-oic acid [II] was separated as another active component of the plant, by tracing albumin stabilizing activity. $IC_{50}$ of [II] for the protein stabilizing activity was 0.026mg/3ml, when those of [I] and phenylbutazone were 0.032 and 0.32 mg/3ml, respectively. Being investigated employing carrageenin-induced edema test in rat hind paw, the anti-inflammatory activity of [II] administered s. c. was slightly lower than that of phenylbutazone, whereas the activity of [II] administered p. p. was three times greater than that of phenylbutazone. These results of [II] were contrary to those of [I] in the aspect of administration routes.

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Platelet Anti-aggregatory Effects of Coumarins from the Roots of Angelica genuflexa and A. gigas

  • Lee, Yong-Yook;Lee, Sang-Hyun;Jin, Jing-Ling;ChoiYun, Hye-Sook
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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    • pp.196.1-196.1
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    • 2003
  • Angelica genuflexa (Umbelliferae) is a perennial herbaceous plant which has also been variously reported as A. koreana and Ostericum koreanum. The MeOH extract was reported to have strong anti-thrombotic potential in the acute thrombosis model. In our preliminary testing, the MeOH extract and one of the solvent fractions (90% MeOH fr.) were observed to have both platelet anti-aggregating and anti-coagulant effects. Five coumarins, isoimperatorin (1), pabulenol (2), isooxypeucedanin (3), oxypeucedanin hydrate (4) and osthol (5) were isolated from the MeOH extract of Angelica genuflexa in the course of searching for anti-platelet and anti-coagulant components. (omitted)

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Phytochemical Constituents of the Leaves of Hosta longipes

  • Kim, Chung Sub;Kim, Ki Hyun;Lee, Kang Ro
    • Natural Product Sciences
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    • 제20권2호
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    • pp.86-90
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    • 2014
  • Phytochemical investigation of the 80% MeOH extract from the leaves of Hosta longipes resulted in the isolation of sixteen compounds (1 - 16). The structures of the compounds were elucidated by spectroscopic methods to be methyl 10,10-dimethoxydecanoate (1), methyl 10-hydroxy-8E,12Z-octadecadienoate (2), methyl coriolate (3), trans-phytol (4), phytene-1,2-diol (5), phyton (6), (3S,5R,6S,7E,9R)-7-megastigmene-3,6,9-triol (7), (3S,5R,6S,9R)-3,6,9-trihydroxymegastigman-7-ene (8), shikimic acid (9), p-coumaramide (10), trans-N-p-coumaroyltyramine (11), cis-N-coumaroyltyramine (12), tryptophan (13), thymidine (14), adenosine (15), and deoxyadenosine (16). Compound 1 was synthesized, but not yet isolated from natural source, and compounds 2-16 were isolated for the first time from this plant source.

약제별 및 살포시기별 자두 검은점무늬병 방제효과 (Control Efficacy of Different Types of Chemicals with Different Spraying Schedules on Plum Bacterial Black Spot)

  • 류영현;이중환;권태영;김승한;김동근
    • 식물병연구
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    • 제18권4호
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    • pp.349-353
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    • 2012
  • 자두 검은점무늬병은 Xanthomonas arboricola pv. pruni에 의한 세균성 병해로 과실표면에 검은 반점형태의 병징이 발생하여 과실 상품성을 저하시켜 자두 재배농가에 큰 경제적 손실을 초래하는데 이러한 자두 검은점무늬병에 대한 효과적인 약제 방제체계를 개발하기 위하여 몇 종의 화학약제와 살포체계를 구성하여 휴면기중에는 동제 약제를 그리고 과실생육기중에는 항생제계열 약제를 살포하였는데 과실생육기중에서의 항생제계열 약제살포는 휴면기중의 동제 약제살포보다 높은 방제효과를 나타내었다. 자두의 개화만개 10일 후부터 10일 간격으로 3회의 항생제계열 약제살포는 93%의 높은 방제가를 얻을 수 있었는데 비해서 휴면기중의 동제 약제살포는 26-42%의 낮은 방제가를 얻는데 그쳤다. 또한 항생제계열 약제의 처음 살포시기가 개화만개 후 20일이나 30일 보다는 개화만개 후 10일에서 더 높은 방제효과를 얻을 수 있었다.

한국 자생식물 추출물 23종의 Aldo-keto reductase family 1 B10 (AKR 1 B10) 효소 억제효과 (Inhibitory Effects of 23 Korean Local Plant Extracts on Aldo-keto reductase family 1 B10 (AKR 1 B10))

  • 이주영;송대근;정상훈;김종환;안수용;노주원;판철호
    • 생약학회지
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    • 제40권3호
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    • pp.238-243
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    • 2009
  • We examined ethanol extracts prepared from 23 Korean local plants obtained in Pyeongchang, Gangwon-do for their inhibitory effects on recombinant human AKR 1 B10 (rhAKR1B10) in vitro. To do this, rhAKR1B10 was first expressed in E. coli as a biological active form and purified by using Ni-affinity chromatography followed by gel permeation chromatography. Then, rhAKR1B10 was used for screening out 23 Korean local plant extracts having an inhibitory activity against itself. Among them, six extracts showed more than 50% inhibition of rhAKR1B10 activity at the concentration of $10{\mu}g$/ml. Especially, the extracts of Ligularia fischeri var. spiciformis Nakai and Rhus trichocarpa Miq. were the most potent because their $IC_{50}$ values were 2.94 and $2.00{\mu}g$/ml, respectively.