• 제목/요약/키워드: (+)-pinoresinol

검색결과 39건 처리시간 0.029초

연교 추출물 Pinoresinol와 Tamiflu의 병용효과로부터 Influenza Virus 감염에 의한 세포사멸 억제효과 (The Combined Anti-apoptotic Effect from Tamiflu and Pinoresinol of Forsythia fructus Extract Against Influenza Virus Infection)

  • 김상태;김장수;최영웅;김영균
    • 생약학회지
    • /
    • 제42권1호
    • /
    • pp.9-14
    • /
    • 2011
  • The fruit body of Forsythiae Fructus (Oleaceae), a common Korean medical herb, is widely used in the treatment of cold and inflammation. In order to elucidate the action mechanism and the active principles from the plant against anti-influenza virus, the influenza virus hemagglutinin (HA) and neuraminidase (NA) gene RT-PCR and Viral Screening & Identification (VSI) assay were conducted, and the activity against viral replication was also investigated. Consequently, one active constituent, namely pinoresinol showed the in vitro antiviral principle using a cytopathic effect (CPE) reduction method, indicating pinoresinol possessed anti-influenza viral activity. Furthermore, combination of pinoresinol and Tamiflu exhibited higher activities than Tamiflu alone against influenza virus (H3N2) infection. The results suggested that combination of pinoresinol with Tamiflu could be a better candidate for an ant-H3N2 viral agent in the treatment of the influenza.

천연에서부터 제초활성물질의 탐색 - 제2보 둥근잎가정큰나무(Rhathiolepis ovata Briat)로 부터 Pinoresinal의 단리 및 생물활성 (The Search for Naturally Occurring Herbicidal Compounds - II. Isolation of Pinoresinol from Rhathiolepis ovata Briat and Its Biological Activity)

  • 안종웅;최정섭;조광연
    • 한국잡초학회지
    • /
    • 제9권1호
    • /
    • pp.76-79
    • /
    • 1989
  • 둥근잎가정큰나무(Rhathiolepis ovata Briat)에 함유된 발아억제물질을 정제하는 과정에서 강한 활성을 나타내는 주 활성본체의 함유량이 미량(1 ppm 이하)임을 발견하고, 이 물질의 효율적인 분리방법을 모색키 위하여 그 구조에 대한 지견을 얻을 목적으로 각종 chromatography 상에서 이 활성 본체와 유사한 거동을 나타내는 물질의 존재를 확인하여 분리한 후, 구조를 분석한 결과 pinoresinol 임을 알수 있었다. 이에 따라 pinoresinol이 둥근잎가정큰나무에 존재한다는 사실이 처음으로 밝혀지게 되었으며 pinoresinol의 공시종자에 대한 발아억제활성은 논피, 바랭이, 참방동사니, 큰달맞이꽃의 종자에는 안정되지 않았으나, 쇠비름종자에 대해서는 5000 ppm에서 55% 정도 발아를 억제시켰다.

  • PDF

Antitumor and Antiinflammatory Constituents from Celtis sinensis

  • Kim Dae Keun;Lim Jong Pil;Kim Jin Wook;Park Hee Wook;Eun Jae Soon
    • Archives of Pharmacal Research
    • /
    • 제28권1호
    • /
    • pp.39-43
    • /
    • 2005
  • Eight compounds were isolated from the methanolic extract of the twigs of Celtis sinensis through repeated silica gel and Sephadex LH-20 column chromatography. Their chemical structures were elucidated as two triterpenoids, germanicol and epifriedelanol, two amide compounds, trans-N-caffeoyltyramine and cis-N-coumaroyltyramine, two lignan glycoside, pinoresinol glycoside and pinoresinol rutinoside, and two steroids by spectroscopic analysis.

개오동나무 잎으로부터 항산화 활성을 갖는 lignan 화합물의 분리 및 동정 (Isolation and identification of lignans as Antioxidant from loaves of Catalpa ovata G. $D_{ON}$)

  • 국주희;마승진;문제학;박근형
    • KSBB Journal
    • /
    • 제18권6호
    • /
    • pp.511-516
    • /
    • 2003
  • 개오동나무 (Catalpa ovata G. Don) 잎의 MeOH 추출물은 DPPH 라디칼 소거활성을 나타냈으며, 이에 개오동나무 잎에 함유된 항산화물질을 구명하고자 하였다. MeOH 추출물을 용매분획하여 EtOAc 가용 중성획분을 얻고, silica gel adsorption column chromatography, Sephadex LH-20 column chromatography로 정제한 다음 HPLC에 의해 3종의 활성물질을 단리하였다. 단리된 물질들은 HR-MS, 1H-NMR, 13C-NMR, 2D-NMR 등의 기기분석에 의해 piperitol, pinoresinol, lariciresinol로 동정하였다. 이들 물질들을 대상으로 DPPH 라디칼 소거활성을 조사한 결과, lariciresinol ($SC_{50}$/, 19$\mu\textrm{g}$/mL) > pinoresinol ($SC_{50}$/, 31$\mu\textrm{g}$/mL) > piperitol ($SC_{50}$/, 59$\mu\textrm{g}$/mL)의 순으로 항산화활성이 나타났다.

지역별 두중(杜仲)의 지표성분 및 항산화 활성 비교 (Comparison of Anti-oxidant Activity and Marker Compounds in Eucommiae Cortex Samples from Regional Groups)

  • 유옥철;최성률;주환수;한창;문혜연;정화진;정찬헌
    • 대한본초학회지
    • /
    • 제33권6호
    • /
    • pp.29-34
    • /
    • 2018
  • Objectives : It is necessary to manage herbal medicines based on effectiveness by comparing the efficacy of herbal medicines by region. In this study, we compared anti-oxidative activity and marker compounds of Eucommiae Cortex by regional groups. Methods : Eucommiae Cortex grown and harvested in Gangjin, Sancheong, Yeongwol, Jangsu, and Jecheon were used. Eucommiae Cortex was extracted in distilled water at $100^{\circ}C$ for 3 hours, and filtered. filtered. Extract samples were freeze-dried at $-80^{\circ}C$. Comparison of anti-oxidant activity in Eucommiae Cortex samples from regional groups was measured in 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging, 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) free radical scavenging, and ferric reducing antioxidant power (FRAP) between regional groups of Eucommiae Cortex. In addition, high-performance liquid chromatography (HPLC) analysis was conducted to compare pinoresinol diglucoside concentration by regional groups. Results : HPLC analysis found that pinoresinol diglucoside concentration, widely known as the marker compound of Eucommiae Cortex, was the highest in Gangwon Yeongwol. There was a significant difference in anti-oxidative activity of Eucommiae Cortex between regional groups as discovered in DPPH, ABTS and FRAP assays. DPPH free radical scavenging was the highest in Jeonbuk Jangsu. ABTS free radical scavenging was the highest in Jeonbuk Jangsu and Chungbuck Jecheon. FRAP was the highest in Jeonbuk Jangsu. Conclusions : Although pinoresinol diglucoside concentration was high, anti-oxidative activity was not proportionately high. Pinoresinol diglucoside concentration was the highest in Gangwon Yeongwol. Anti-oxidative activity was the highest in Jeonbuk Jangsu.

Lignans from Lonicerae caulis

  • Yean, Min-Hye;Kim, Ju-Sun;Lee, Je-Hyun;Kang, Sam-Sik
    • Natural Product Sciences
    • /
    • 제16권1호
    • /
    • pp.15-19
    • /
    • 2010
  • A new 2,7'-cyclolignan named lonicerinol (1) along with eight known lignans, (-)-epipinoresinol (2), (-)-pinoresinol (3), $9{\alpha}$-hydroxypinoresinol (4), 7R,8S-dihydrodehydrodiconiferyl alcohol (5), ($\pm$)-neo-olivil (6), (+)-isolariciresinol (7), 3-methoxy-8,4'-oxyneoligna-3',4,7,9,9'-pentol (8), and (-)-pinoresinol 4-O-glucoside (9), were isolated from the caulis of Lonicera japonica THUNB. (Caprifoliaceae). All of these constituents except for (-)-pinoresinol (3) and $9{\alpha}$-hydroxypinoresinol (4) are reported for the first time from the genus Lonicera. The structures and absolute configurations of these compounds were determined on the basis of spectroscopic analysis, including CD and 1D- and 2D-NMR techniques and chemical methods.

Lignans of Rosa multiflora Roots

  • Yeo, Hosup;Chin, Young-Won;Park, Shin-Young;Kim, Jin-Woong
    • Archives of Pharmacal Research
    • /
    • 제27권3호
    • /
    • pp.287-290
    • /
    • 2004
  • Five known lignans, (+)-pinoresinol (1), (+)-8-hydroxypinoresinol (2), (-)- dehydrodiconiferyl alcohol (3), (+)-trans-dehydrodiconiferyl alcohol (4), and (-)-olivil (5), were isolated from the roots of Rosa multiflora for the first time. Their structures were determined using spectroscopic data.

LPS로 유도된 RAW 264.7 세포의 염증반응에서 감송향(甘松香)에서 추출한 8α-hydroxy pinoresinol의 항염증 효과 (Anti-inflammatory Effects of 8α-hydroxy pinoresinol isolated from Nardostachys jatamansi on Lipopolysaccharide-induced Inflammatory Response in RAW 264.7 Cells.)

  • 최선복;박성주
    • 대한본초학회지
    • /
    • 제31권5호
    • /
    • pp.1-6
    • /
    • 2016
  • Objectives : Nardostachys jatamansi (NJ) is a medicinal herb that has been reported in various traditional systems of medicine for its use in antispasmodic, a digestive stimulant, skin diseases. Previous studies have already reported that NJ effectively protects against inflammation. However, the active compound in NJ is unknown. Therefore, in the present study, we analyzed effects of a compound, 8α-hydroxy pinoresinol (HP), isolated from NJ against lipopolysaccharide (LPS) induced inflammation in RAW 264.7 cells.Methods : To examine the anti-inflammatory effect of HP against LPS, intraperitoneally pre-treat the HP (100, 200, 500 and 1,000 nM) 1 h prior to LPS challenges. LPS was stimulated with 500 ng/ml in RAW 264.7 cells. To identify the anti-inflammatory effect of HP, we measured inflammatory mediators such as inducible nitric oxide synthase (iNOS) and its derivative nitric oxide (NO), cyclooxygenase-2 (COX-2), prostaglandin E2 (PGE2). Also we evaluated molecular mechanisms including mitogen-activated protein kinases (MAPKs) and nuclear factor-kappaB (NF-κB) activation by western blot.Results : The HP inhibited production of inflammatory mediators, such as iNOS and its derivative NO, COX-2 and PGE2 in LPS- induced inflammationin RAW 264.7 cells. Additionally, HP also inhibited activation of p38 pathway signaling but not extracellularsignal-regulatedkinase (ERK), c-jun NH2-terminal kinase (JNK), and NF-κB.Conclusion : Our results suggest that HP has anti-inflammatory functions through the dephosphorylation of p38 and HP can provide beneficial strategy for prevention and therapy of inflammation.

SJ004의 추출용매별 항산화 활성 및 표준화 연구 (Antioxidant Activity and Standardization of Extraction Solvents of SJ004)

  • 이대연;조주휘;김완수;이호성;이영우;박상인;안건상;이인희
    • 한방재활의학과학회지
    • /
    • 제30권2호
    • /
    • pp.67-75
    • /
    • 2020
  • Objectives SJ004 is a natural herbal medicine that contains Acyranthes japonica Nakai and Eucommia ulmoides Oliver traditionally used for joint and spinal diseases. This study aimed to establish an efficient method of extracting SJ004 to standardize using the yield, high-performance liquid chromatography (HPLC), and antioxidant assay. Methods SJ004 was extracted with distilled water, 70% and 100% of ethyl alcohol (EtOH). The method validation of 20-hydroxyecdysone and pinoresinol diglucoside was determined by HPLC-photo diode array and the content of SJ004 was calculated. The antioxidant activity of each extract was compared and measured using total flavonoids, total phenolic compounds, 2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid), and ferric reducing antioxidant power according to the standard protocol. Results The yield was highest in pure water extract and lowest in 100% EtOH. But, the content of marker compounds indicating 20-hydroxyecdysone and pinoresinol diglucoside was highest in 100% EtOH extract. In the physiological activity measurement using antioxidant activity, 100% ethanol extract was highest. The limit of detection indicating 20-hydroxyecdysone and pinoresinol diglucoside were analyzed 0.33 ㎍/mL, 0.1616 ㎍/mL, and the limit of quantification were analyzed 1.01 ㎍/mL and 0.49 ㎍/mL respectively. Conclusions The experimental results showed that the extraction conditions have a significant effect on content of marker compounds and antioxidant activity. As a result of method validation, SJ004 was standardized by 20-hydroxyecdysone and pinoresinol diglucoside.

포제에 따른 두충의 지표성분 함량분석 (Quantitative Determination of the Six Marker Compounds in Eucommiae Cortex by Processing Method)

  • 서창섭;김정훈;신현규;김병수
    • 생약학회지
    • /
    • 제46권2호
    • /
    • pp.123-132
    • /
    • 2015
  • In this study, we carried out quantification analysis of the six marker components, geniposidic acid, chlorogenic acid, geniposide, pinoresinol diglucoside, liriodendrin, and genipin in the 70% ethanol extracts of non-processed Eucommiae Cortex and processed Eucommiae Cortex using a high-performance liquid chromatography coupled with photodiode array detector. The six components were separated on Gemini C18 column (5 μm, 4.6×250 mm) by the gradient elution with 1.0% (v/v) acetic acid in water and 1.0% (v/v) acetic acid in acetonitrile as mobile phase. The flow rate was 1.0 mL/min and the injection volume was 10 mL. The amount of geniposidic acid, chlorogenic acid, geniposide, pinoresinol diglucoside, liriodendrin, and genipin in non-processed Eucommiae Cortex were 1.31, 0.31, 0.66, 0.46, 0.46, and 0.03%, respectively, while the amount of the six compounds in non-processed Eucommiae Cortex were 0.04-0.78, 0.01-0.14%, 0.05-0.63%, 0.01-0.37%, 0.15-0.42%, and not detected, respectively. After processing treatment, the contents of three iridoids, two lingnan, and one phenylpropanoid decreased in Eucommiae Cortex.